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WO2024246354A1 - Peptides à activité lipolytique, anti-lipogène, antifibrotique et anti-inflammatoire - Google Patents

Peptides à activité lipolytique, anti-lipogène, antifibrotique et anti-inflammatoire Download PDF

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Publication number
WO2024246354A1
WO2024246354A1 PCT/EP2024/065136 EP2024065136W WO2024246354A1 WO 2024246354 A1 WO2024246354 A1 WO 2024246354A1 EP 2024065136 W EP2024065136 W EP 2024065136W WO 2024246354 A1 WO2024246354 A1 WO 2024246354A1
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Prior art keywords
peptide
seq
pharmaceutically acceptable
acceptable salt
fragment
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English (en)
Inventor
David Martinez Selva
Rafael SIMÓ CANONGE
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Endolipid Therapeutics SL
Fundacio Institut de Recerca Hospital Universitari Vall dHebron
Original Assignee
Endolipid Therapeutics SL
Fundacio Institut de Recerca Hospital Universitari Vall dHebron
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Priority to AU2024280725A priority Critical patent/AU2024280725A1/en
Publication of WO2024246354A1 publication Critical patent/WO2024246354A1/fr
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
    • C07K14/4717—Plasma globulins, lactoglobulin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Definitions

  • Peptides with lipolytic, anti-lipogenic, antifibrotic and anti-inflammatory activity are Peptides with lipolytic, anti-lipogenic, antifibrotic and anti-inflammatory activity.
  • the present invention relates to the field of peptides and their medical use in therapy of diseases associated to the accumulation of fat in an organ, to inflammation and/or fibrosis, in particular in the therapy of Nonalcoholic fatty liver disease (NAFLD) and obesity. It also relates to their use in cosmetics.
  • NAFLD Nonalcoholic fatty liver disease
  • Non-alcoholic fatty liver disease is a leading cause of liver-related morbidity and mortality. It affects between 17% and 46% of adults. It is characterized by the accumulation of fat inside the liver cells, which causes inflammation and scarring of the organ.
  • NAFLD encompasses a spectrum of conditions which ranges from fatty liver to cirrhosis.
  • the main stages of NAFLD are (I) fatty liver (steatosis), (II) non-alcoholic steatohepatitis (NASH), (ill) hepatic fibrosis, and (iv) cirrhosis.
  • Fatty liver is characterized by an excess of fat in the liver but very little or no inflammation or cell damage.
  • accumulation of fat is accompanied by inflammation and liver cells damage.
  • Inflammation and cell damage can lead to scarring and the appearance of fibrosis.
  • persistent inflammation can cause scar tissue formation and hepatic fibrosis, which can ultimately lead to cirrhosis.
  • NAFLD ha a complex pathophysiology, that includes lipid accumulation, inflammation and fibrosis.
  • NAFLD neurodegenerative disease
  • NAFLD The main treatment of NAFLD consist in reducing corporal weight. Weight loss can reduce fat, inflammation, and fibrosis— or scarring— in the liver. However, apart from controlling the conditions that contribute to fatty liver disease, efficient treatments of NASH are missing.
  • SHBG sex hormone- binding globulin
  • the invention relates to a peptide or a pharmaceutically acceptable salt thereof, wherein the peptide has a length of 9 to 49 amino acids, each one of the amino acids being L- or D-amino acid and comprises: a peptide fragment F1 with a length of 4-10 amino acids, each one of the amino acids being L- or D-amino acid, and with sequence
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A
  • X 3 represents D or N
  • X 4 represents P, N, a basic amino acid or a hydrophobic amino acid, preferably P, N, L, V, or A,
  • X 5 represents E or Q
  • X 6 and X 7 are the same or different and represent A, V, L or I,
  • X 8 represents F or P
  • subindexes "a”, “b”, “c”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1 and at least two of them represent 1
  • the peptide further comprises:
  • a peptide fragment F2 at the N-terminal end of peptide fragment F1 with a length of 5 to 19 amino acids, each one of the amino acids being L- or D-amino acid, and that comprises sequence SEQ ID NO.2 (SF(X 9 )VR), wherein X 9 represents E or Q, and/or ii) a peptide fragment F3 at the C-terminal end of peptide fragment F1 , with a length of 10 to 20 amino acids, each one of the amino acids being L- or D-amino acid, and that comprises SEQ ID NO.
  • GDTNPKDDWF GDTNPKDDWF
  • the peptide has a length of 10-40 amino acids, and consists of a peptide fragment F1 and, additionally: of a peptide fragment F2 at the N-terminal end of peptide fragment F1 and/or of a peptide fragment F3 at the C-terminal end of peptide fragment F1, wherein,:
  • peptide fragment F1 has SEQ ID NO. 9: TWDPEGVIFY or is a variant thereof that has at least 80% sequence identity with SEQ ID NO.9, wherein each one of the amino acids of peptide fragment F1 is a L- or D-amino acid; ii) peptide fragment F2 has SEQ ID NO. 13 (TKTSSSFEVR) or is a variant thereof with at least 80% sequence identity with SEQ ID NO.13; or has SEQ ID NO.
  • VMTFDLTKITKTSSSFEVR or is a variant thereof with at least 80% sequence identity with SEQ ID NO.14; and wherein each one of the amino acids of peptide fragment F2 is a L- or D-amino acid; and ill) peptide fragment F3 has SEQ ID NO. 4 (GDTNPKDDWF) or is a variant thereof with at least 80% sequence identity with SEQ ID NO.4; or has SEQ ID NO. 15 (GDTNPKDDWFMLGLRDGRPE) or is a variant thereof with at least 90% sequence identity with SEQ ID NO.15; and wherein each one of the amino acids of peptide fragment F3 is a L- or D-amino acid.
  • GDTNPKDDWF GDTNPKDDWF
  • MGLRDGRPE GDTNPKDDWFMLGLRDGRPE
  • peptides falling within the scope of the first aspect have the advantageous effects mentioned above (lipolytic, anti-lipogenic, antifibrotic and anti-inflammatory).
  • peptide with SEQ ID NO. 16 reduces the mRNA expression of key hepatic lipogenic enzymes in HepG2 cells, reduces collagen fibrosis (collagen 1 A expression) induced by TGFpl in LX-2 cells, and induces lipolysis in adipocytes (see example 3).
  • mice that received subcutaneous administration of the peptide with SEQ ID NO.16 while being treated to develop obesity and fatty liver disease showed a reduction of total body weight gain, liver weight, subcutaneous and visceral adipose tissue, of the expression of different indicators of hepatic lipogenesis and of hepatic lipid accumulation, reduced steatosis scores, and reduced hepatic inflammation as compared to control mice simply treated to develop obesity and fatty liver disease but with no SEQ ID NO. 16 peptide administration.
  • the authors of the present invention have shown that peptide with SEQ ID NO. 16, prevents the development of symptoms associated to obesity and NAFLD in an animal model of the diseases, including lipid accumulation, fibrosis and inflammation.
  • Example 6 a mouse model of obesity and fatty liver disease that received subcutaneous administration of SEQ ID NO. 16 showed a reduction of body weight gain, of liver weight, of serum levels of glucose, Alanine transaminase (ALT) and Aspartate transaminase (AST), of hepatic lipid accumulation and of hepatic lipogenesis indicators, of steatosis scores, as well as a reduction in hepatic and adipose tissue inflammation as compared to obesity and fatty liver disease mouse model that did not receive SEQ ID NO. 16 administration.
  • mouse model that received SEQ ID NO. 16 administration did not show hepatic fibrosis, contrary to those with no SEQ ID NO. 16 administration.
  • the authors of the present invention have shown that peptide with SEQ ID NO. 16 can revert the symptomatology associated to obesity and NAFLD in an animal model of the diseases, in particular lipid accumulation, fibrosis and inflammation.
  • the invention in a second aspect, relates to a pharmaceutical composition
  • a pharmaceutical composition comprising a therapeutical effective amount of the peptide, or pharmaceutically acceptable salt thereof, according to the first aspect of the invention, and one or more therapeutically acceptable carriers.
  • the invention relates to the peptide, or a pharmaceutically acceptable salt thereof, according to the first aspect of the invention, or the pharmaceutical composition according to the second aspect of the invention, for use in therapy.
  • the invention relates to the peptide, or a pharmaceutically acceptable salt thereof, according to the first aspect of the invention, or the pharmaceutical composition according to the second aspect of the invention, for use in the treatment and/or prevention of a condition or disease caused or associated to the accumulation of fat in an organ or tissue, particularly in an organ, inflammation and/or fibrosis.
  • the invention relates to a cosmetic composition
  • a cosmetic composition comprising the peptide, or pharmaceutically acceptable salt thereof, of the first aspect of the invention, and one or more cosmetically acceptable carriers.
  • the invention relates to the use of the peptide or a pharmaceutically acceptable salt thereof, according to the first aspect of the invention, or the cosmetic composition according to the fifth aspect of the invention, in cosmetics.
  • the invention relates to a kit of parts comprising: a peptide, or pharmaceutically acceptable salt thereof, according to the first aspect of the invention, the pharmaceutical composition according to the second aspect of the invention, or the cosmetic composition according to the fifth aspect of the invention, and a device selected from the group consisting of an injection device, an implant, or a biodegradable container.
  • the invention relates to a device, such as an injection device, an implant, or a biodegradable container, comprising the peptide or pharmaceutically acceptable salt thereof according to he first aspect, the pharmaceutical composition according to the second aspect of the invention, or the cosmetic composition according to the fifth aspect of the invention.
  • Fig. 1 shows the peptide synthesis flow.
  • Fig. 2 Human hepatoblastoma cell line HepG2 was treated with vehicle (DMSO) in the absence or presence of 30mM fructose and Telmisartan (5pg/ml), Semaglutide (1 OnM) or GP6 (10 or 40pig/ml) for 5 days. RNA was extracted and mRNA levels of Acetyl-CoA Carboxylase (ACC) (panel A) and Peroxisome proliferator- activated receptor gamma (PPARy) (panel B) relative to 18S were measured by RTPCR.
  • ACC Acetyl-CoA Carboxylase
  • PPARy Peroxisome proliferator- activated receptor gamma
  • Fig. 3 Human hepatic stellate cell line LX-2 was treated with vehicle (DMSO) or TGF
  • Fig. 4 Mature human subcutaneous adipocytes were treated with vehicle (DMSO), 1 piM of Isoproterenol, Semaglutide (10nM) or GP6 (25, 50 or 100pig/ml) for 16h. Glycerol concentration was assessed using a Lipolysis Assay Kit (Tebu-bio).
  • Fig. 5 Human hepatoblastoma cell line HepG2 was treated with vehicle (DMSO) or 1 O M of GP4, GP7, GP8 or GP9 for 24h. RNA was extracted and mRNA levels of Acetyl-CoA Carboxylase (ACC), Fatty Acid Synthase (FAS) and ATP-Citrate Lyase (ACLY) relative to 18S were measured by RTPCR.
  • ACC Acetyl-CoA Carboxylase
  • Fatty Acid Synthase Fatty Acid Synthase
  • ACLY ATP-Citrate Lyase
  • Fig. 6 Human hepatic stellate cell line LX-2 was treated with vehicle (DMSO) or TGF
  • vehicle DMSO
  • 31 10ng/ml
  • Fig. 7 Mature human subcutaneous adipocytes were treated with vehicle (DMSO), 3pi M of Isoproterenol or 1 O M of GP4, GP8 or GP9 for 16h. Glycerol concentration was assessed using a Lipolysis Assay Kit (Tebu- bio). Lipolysis induction was calculated with respect to the control cells treated with DMSO.
  • vehicle DMSO
  • 3pi M of Isoproterenol or 1 O M of GP4, GP8 or GP9 for 16h.
  • Glycerol concentration was assessed using a Lipolysis Assay Kit (Tebu- bio). Lipolysis induction was calculated with respect to the control cells treated with DMSO.
  • Fig. 8 Total body weight (panel A) and body weight increment (panel B) were measured at the end of the experiment in vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • FIG. 9 Liver (panel A) and adipose tissue from subcutaneous (panel B), visceral (panel C) and brown (panel D) origin were weighed at the end of the experiment in vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 10 H&E histological examination of livers from vehicle and GP6 treated mice at the end of the experiment. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • FIG. 11 Liver triglyceride (TAG) content (panel A) of vehicle and GP6 treated mice at the end of the experiment. Brunt score (panel B), Steatosis (panel C) and % of steatosis (panel D) were analyzed in H&E histological sections. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 12 Peroxisome Proliferator Activator Receptor gamma (PPARY) (panel B), Acetyl-CoA Carboxylase (ACC) (panel A) and Fatty Acid Synthase (FAS) (panel C) mRNA levels relative to 18S were measured by RTPCR in livers from vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 13 F4/80 (panel D), TNFo (panel A), IL1 p (panel B) and IL6 (panel C) mRNA levels relative to 18S were measured by RTPCR in livers from vehicle and GP6 treated mice.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • Fig. 14 F4/80 mRNA levels relative to 18S were measured by RTPCR in adipose tissue of control, vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Col1A1 mRNA levels relative to 18S were measured by RTPCR in adipose tissue of control, vehicle and GP6 treated mice.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • FIG. 16 Body weight increment (panel A) and liver weight (panel B) were measured at the end of the experiment in vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • AST (panel A) and ALT (panel B) activity levels in serum were measured at the end of the experiment in vehicle and GP6 treated mice.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • Fig. 18 Picrosirius staining of livers from vehicle and GP6 treated mice at the end of the experiment (panel A), collagen staining pointed by black arrows.. Picrosirius red quantification using Imaged software of all sections (Panel B). Fibrosis stage determination by the pathologist of all sections. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Col1A1 mRNA levels relative to 18S were measured by RTPCR in livers of vehicle and GP6 treated mice.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • Fig. 20 F4/80 mRNA levels relative to 18S were measured by RTPCR in livers of vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 21 Total body weight (panel A) and liver weight (panel B) were measured at the end of the experiment in control, vehicle, Telmisartan and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Glucose and AST activity levels in serum were measured at the end of the experiment in control, vehicle, Telmisartan and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 23 H&E histological examination of livers from control, vehicle and GP6 treated mice at the end of the experiment. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 24 Liver triglyceride (TAG) content (panel A) of control, vehicle, Telmisartan and GP6 treated mice at the end of the experiment. Steatosis (panel C) and Brunt score (panel B) analysis were performed in H&E histological sections. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • TAG Liver triglyceride
  • Fig. 25 Peroxisome Proliferator Activator Receptor gamma (PPARY) (panel A) and Acetyl-CoA Carboxylase (ACC) (panel B) mRNA levels relative to 18S were measured by RTPCR in livers of control, vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 26 Picrosirius staining of livers of control, vehicle and GP6 treated mice at the end of the experiment.
  • White arrows show normal collagen deposits and black arrows show collagen deposits from increase hepatic fibrosis.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • FIG. 27 Col1A1 (panel A) and TGFpl (panel B) mRNA levels relative to 18S were measured by RTPCR in livers of control, vehicle and GP6 treated mice.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • Fig. 28 F4/80 (panel A) and TNFo mRNA levels relative to 18S were measured by RTPCR in livers of control, vehicle and GP6 treated mice.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • Fig. 29 F4/80 (panel A) and IL1 p (Panel B) mRNA levels relative to 18S were measured by RTPCR in livers of control, vehicle and GP6 treated mice.
  • Mpk mg/kg
  • SC subcutaneous administration
  • QD once a day administration.
  • Fig. 30 Col1A1 mRNA levels relative to 18S were measured by RTPCR in adipose tissue of control, vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 31 Col1A1 mRNA levels relative to 18S were measured by RTPCR in heart of control, vehicle and GP6 treated mice. Mpk: mg/kg; SC: subcutaneous administration; QD: once a day administration.
  • Fig. 32 Effect of GP6 and modified peptides on hepatic lipogenesis in HepG2 cells. Each bar within each group represents mRNA levels of a key hepatic lipogenic enzyme, from left to right: Acetyl-CoA Carboxylase (ACC), ATP Citrate Lyase (ACLY) and Fatty Acid Synthase (FAS), and a key transcription factor regulating several lipogenic enzymes such as PPARy (PPARy).
  • ACC Acetyl-CoA Carboxylase
  • ACLY ATP Citrate Lyase
  • PPARy a key transcription factor regulating several lipogenic enzymes
  • Fig. 33 Effect of different peptides and SHBG on fibrosis in LX-2 cells.
  • Fig. 34 Effects of different peptides and SHBG in reducing hepatic lipogenic key enzymes in the presence of 30mM fructose.
  • Each bar within each group represents mRNA levels of a key hepatic lipogenic enzyme, from left to right: Acetyl-CoA Carboxylase (ACC), ATP Citrate Lyase (ACLY) and Fatty Acid Synthase (FAS), and a key transcription factor regulating several lipogenic enzymes such as PPARy (PPARy).
  • ACC Acetyl-CoA Carboxylase
  • ACLY ATP Citrate Lyase
  • PPARy a key transcription factor regulating several lipogenic enzymes
  • any ranges given include both the lower and the upper endpoints of the range.
  • the invention relates to a peptide or a pharmaceutically acceptable salt thereof, wherein the peptide has a length of 9 to 49 amino acids, particularly of 10-40 amino acids, each one of the amino acids being L- or D-amino acid, and that comprises peptide fragment F1, and additionally fragment/s F2 and/or F3 as defined above.
  • the peptide of the first aspect has a length of 9 to 49 amino acids, particularly of 10-40 amino acids, each one of the amino acids being L- or D-amino acid, and consists of peptide fragment F1, and additionally fragment/s F2 and/or F3 as defined above. More particularly, the peptide of the first aspect has a length of 10-40 amino acids, and:
  • peptide fragment F1 has SEQ ID NO. 9: TWDPEGVIFY or is a variant thereof that has at least 80% sequence identity with SEQ ID NO.9, wherein each one of the amino acids of peptide fragment F1 is a L- or D-amino acid; ii) peptide fragment F2 has SEQ ID NO. 13 (TKTSSSFEVR) or is a variant thereof with at least 80% sequence identity with SEQ ID NO.13; or has SEQ ID NO.
  • VMTFDLTKITKTSSSFEVR or is a variant thereof with at least 80% sequence identity with SEQ ID NO.14; and wherein each one of the amino acids of peptide fragment F2 is a L- or D-amino acid; and iii) peptide fragment F3 has SEQ ID NO. 4 (GDTNPKDDWF) or is a variant thereof with at least 80% sequence identity with SEQ ID NO.4; or has SEQ ID NO. 15 (GDTNPKDDWFMLGLRDGRPE) or is a variant thereof with at least 80% sequence identity with SEQ ID NO.15; and wherein each one of the amino acids of peptide fragment F3 is a L- or D-amino acid.
  • GDTNPKDDWF GDTNPKDDWF
  • MGLRDGRPE GDTNPKDDWFMLGLRDGRPE
  • peptide refers to the term commonly known by a skilled person.
  • the term refers to short chains of amino acids, typically between 2 and 50 amino acids in length, linked by peptide bonds.
  • Peptide bonds linking the amino acids of a peptide generally form through a dehydration reaction and join the carboxyl group of one amino acid to the amine group of the next amino acid in a head-to-tail manner to form a peptide chain. This leaves a free carboxylic group at one end of the peptide, called the C-terminus, and a free amine group on the other end called the N-terminus.
  • the protein When the protein is translated from messenger RNA, it is created from N-terminus to C-terminus.
  • the convention is to write the amino acid sequence of the peptide from N- to C-terminus, and thus to put the C-terminal end on the right.
  • fragment F2 is directly linked to the N-terminus of fragment F1.
  • the peptide of the invention does not comprise fragment F3, and fragment F2 is directly linked to the N-terminus of fragment F1 .
  • the peptide of the invention consists of fragment F2 and fragment F1 and fragment F2 is directly linked to the N-terminus of fragment F1.
  • fragment F3 is directly linked to the C-terminus of fragment F1.
  • the peptide of the invention does not comprise fragment F2 and fragment F3 is directly linked to the C-terminus of fragment F1 .
  • the peptide of the invention consists of fragments F1 and fragment F3 and fragment F3 is directly linked to the C-terminus of fragment F1.
  • the peptide of the invention comprises fragments F2, F1 and F3 and fragment F2 is directly linked to the N-terminus of fragment F1 and fragment F3 is directly linked to the C-terminus of fragment F1.
  • the peptide consists of fragments F2, F1 and F3 and fragment F2 is directly linked to the N-terminus of fragment F1 and fragment F3 is directly linked to the C-terminus of fragment F1 .
  • the term “directly linked”, as used herein, refers to the fact that the C-terminal amino acid of a peptide fragment (i.e. the last amino acid of the amino acid chain of the peptide) is linked to the N-terminal amino acid of another peptide fragment (the first amino acid of the amino acid chain of said peptide) by a peptide bond.
  • the term “directly linked” in the context of two peptide fragments refers to the fact that the two fragments are directly linked by a peptide bond.
  • the term “directly linked” in the context of two peptide fragments refers to the fact that the C-terminal amino acid of one fragment is linked to the N-terminal amino acid of the other fragment by a peptide bond.
  • peptide fragment F2 is linked to the N-terminus of peptide fragment F1 by a peptide bond, particularly by a peptide bond between the C-terminal amino acid of fragment F2 and the N-terminal amino acid of fragment F1.
  • peptide fragment F3 is linked to the C-terminus of peptide fragment F1 by a peptide bond, particularly by a peptide bond between the C-terminal amino acid of fragment F1 and the N-terminal amino acid of fragment F3.
  • length of a peptide refers to the number of amino acids forming said peptide or peptide fragment.
  • a peptide with a length of 4-10 amino acids is peptide that has 4-10 amino acids
  • a peptide with a length of 15 amino acids is a peptide that has 15 amino acids or whose number of amino acids is 15. Therefore, the expression “the peptide has a length of 9 to 49 amino acids” or “the peptide has 9 to 49 amino acids”, or a "peptide with a length of 9-49 amino acids” as used herein, refers to a peptide whose number of amino acids is of 9-49.
  • the peptide of the invention has a length of 9-49, 10-49, 11-49, 12-49, 13-49, 14-49, 15- 49, 16-49, 17-49, 18-49, 18-49, 19-49 or 20-49 amino acids, particularly 14-49.
  • the length of the peptide of the invention is of 15-49.
  • the length of the peptide of the invention is of 20-49.
  • the length of the peptide of the inventions is of 10-48, 11-48, 12-48, 13-48, 14-48, 15-48, 16-48, 17-48, 18-48, 18-48, 19-48 or 20-48 amino acids, more particularly, 10-48 amino acids.
  • the peptide of the invention has a length of 9-49, 9-48, 9-47, 9-46, 9-45, 9-44, 9-43, 9-42, 9-41 , 9-40, 9-39-, 9-38, 9-37, 9-36, 9-35, 9-34,9-33, 9-32, 9-31 , 9-30, 9-29, 9-28, 9-27, 9-26, 9-25, 9-24, 9-23, 9-22, 9-21 , 9-20 amino acids, particularly 9-30 amino acids.
  • the peptide of the invention has a length of 10-48, 11-45, 12-40, 12-35, 15- 35, 15-30 amino acids, particularly 15-30 amino acids.
  • the peptide of the invention has a length of 20-30 amino acids. In another embodiment, the peptide of the invention has a length of 15- 20 amino acids. In a more particularly embodiment, the peptide of the invention has a length of 12-35, even more particularly 15-30 amino acids. In another embodiment, the length of the peptide of the invention is selected from the list consisting of 15, 16, 17, 18, 19, 20, 28 and 30 amino acids. In another embodiment, the length of the peptide of the invention is selected from the list consisting of 20, 28, 29 and 30 amino acids. In another more particular embodiment, the length of the peptide of the invention is selected from the list consisting of 20, 29 and 30 amino acids. In another particular embodiment, the peptide of the invention has a length of 20 amino acids.
  • the peptide of the invention has a length of 28 amino acids. In another particular embodiment, the peptide of the invention has a length of 29 amino acids. In another particular embodiment, the peptide of the invention has a length of 30 amino acids.
  • the term "peptide fragment” or “fragment” as used herein refers to a peptide subunit of the corresponding peptide. Thus, said fragment is a short chain of amino acids comprised within a peptide and with a length shorter than that of said peptide, i.e. with a number of amino acids lower than the number of amino acids of said peptide.
  • the peptide fragments referred to as F1 , F2 and F3 herein are amino acid chains that have a length shorter than that of the peptide of the invention.
  • the length of the peptide of the invention is equal or higher than the sum of the lengths of the fragments comprised in the peptide of the invention and that are defined as F1, F2 and F3.
  • the peptide of the invention comprises, in addition to said fragments, additional amino acids.
  • the length of the peptide of the invention is equal to the sum of the lengths of the fragments comprised in the peptide of the invention and that are defined as F1 , F2 and F3. In a particular embodiment, the length of the peptide of the invention is equal or higher than the sum of the lengths of the fragments defined as F1 , F2, and F3 which are comprised in the peptide of the invention. In a particular embodiment, the length of the peptide of the invention is equal to the sum of the lengths of the fragments defined as F1 , F2, and F3 which are comprised in the peptide of the invention.
  • peptide fragment F1 has a length of 4-10, 5-10, 6-10, 7-10, 8-10, or 9-10 amino acids. In a particular embodiment, fragment F1 has a length of 5-10. In a more particular embodiment, fragment F1 has a length of 10 amino acids.
  • peptide fragment F2 has a length of 5-19, 6-19, 7-19, 8-19, 9-19, 10-19, 10-19, 11-19, 12-19, 13-19, 14-19, 15-19, 16-19, 17-19, or 18-19 amino acids. In a particular embodiment, the peptide fragment F2 has a length of 19 amino acids. In another embodiment, the peptide fragment F2 has a length of 5-10, 6-10, 7-10, 8-10, or 9-10 amino acids. In a particular embodiment, peptide fragment F2 has a length of 5, 6, 7, 8, 9 or 10 amino acids, more particularly 10 amino acids.
  • peptide fragment F3 has a length of 10-20, 1 1-20, 12-20, 13-20, 14-20, 15-20, 16-20, 17-20, 18-20, or 19-20 amino acids. In a particular embodiment, fragment F3 has a length of 20 amino acids. In a more particular embodiment, fragment F3 has a length of 10 amino acids.
  • basic amino acid refers to amino acids with side chains containing nitrogen and resembling ammonia which is a base (such as amines, guanidines, or imidazole).
  • bases such as amines, guanidines, or imidazole.
  • Non-limitative examples of basic amino acids are Lys, Arg, and His.
  • the basic amino acids referred herein are Lys, Arg, and/or His.
  • Hydrophobic amino acids refers to amino acids having hydrophobic side chains, which tend to be repelled from water. When part of a protein, these amino acids typically form the hydrophobic core of proteins, which is isolated from the polar solvent.
  • Non-limitative examples of hydrophobic amino acids include glycine (Gly), alanine (Ala), valine (Vai), leucine (Leu), isoleucine (lie), proline (Pro), phenylalanine (Phe), methionine (Met), and tryptophan (Trp).
  • the hydrophobic amino acids referred herein are selected from the list consisting of glycine (Gly), alanine (Ala), valine (Vai), leucine (Leu), isoleucine (lie), proline (Pro), phenylalanine (Phe), methionine (Met), and tryptophan (Trp).
  • the hydrophobic amino acids referred herein are selected from the list consisting of alanine (Ala), valine (Vai), leucine (Leu), isoleucine (lie), proline (Pro), phenylalanine (Phe) and cysteine (Cys).
  • the hydrophobic amino acids referred herein are selected from the list consisting of alanine (Ala), valine (Vai), and leucine (Leu).
  • salt As used herein, the term "pharmaceutically acceptable salt”, or “acceptable salt” or “salt” refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Appropriate acceptable salts are well known in the art.
  • Examples of pharmaceutical acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange.
  • inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid
  • organic acids such as acetic acid, trifluoroacetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange.
  • salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulphate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulphate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulphate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulphate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulphate, 3-
  • Salts derived from appropriate bases include alkali metal, alkaline earth metal, and ammonium.
  • Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like.
  • Further acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulphate, phosphate, nitrate, lower alkyl sulfonate and aryl sulfonate.
  • fragment F1 of the peptide of the invention has a length of 4-10, 5-10, 6-10, 7-10, 8-10, 9-10, or 10 amino acids, more particularly, 4-10 amino acids, each one of the amino acids being L- or D- amino acid, and has a sequence SEQ ID NO. 5: (X 1 ) a (X 2 ) b D (X 4 )E G(X 6 ) d (X 7 ) e (X 8 )f(Y) g , wherein:
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A;
  • X 4 represents P, N or L,
  • X 6 and X 7 are the same or different and represent A, V, L or I;
  • X 8 represents F or P
  • subindexes "a”, “b”, “d”, “e”, “f” and “g”” are integer numbers independently selected from 0 and 1.
  • fragment F1 of the peptide of the invention has a length of 4-10, 5-10, 6-10, 7-10, 8-10, 9-10, or 10 amino acids, more particularly, 4-10 amino acids, each one of the amino acids being L- or D-amino acid, and has a sequence SEQ ID NO. 6: (X 1 ) a (X 2 ) b D P E G(X 6 ) d (X 7 ) e (X 8 )f(Y) g wherein:
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A
  • X 6 and X 7 are the same or different and represent A, V, L or I,
  • X 8 represents F or P, subindexes "a”, “b”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1 ;
  • fragment F1 of the peptide of the invention has a length of 4-10, 5-10, 6-10, 7-10, 8-10, 9-10, or 10 amino acids, more particularly, 4-10 amino acids, each one of the amino acids being L- or D-amino acid, and has a sequence SEQ ID NO. 7: (X 1 ) a (X 2 ) b D L E G(X 6 ) d (X 7 ) e (X 8 )f(Y) g , wherein:
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A
  • X 6 and X 7 are the same or different and represent A, V, L or I;
  • X 8 represents F or P
  • subindexes "a”, “b”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1.
  • peptide fragment F1 of the peptide of the invention has a length of 4-10, 5-10, 6- 10, 7-10, 8-10, 9-10, or 10 amino acids, more particularly, 4-10 amino acids, each one of the amino acids being L- or D-amino acid, and has a sequence SEQ ID NO. 8: (X 1 ) a (X 2 ) b D N E G(X 6 ) d (X 7 ) e (X 8 )f(Y) g . wherein:
  • X 1 represents T, or A
  • X 2 represents W, N, Q K or A
  • X 6 and X 7 are the same or different and represent A, V, L or I;
  • X 8 represents F or P
  • subindexes "a”, “b”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1.
  • the peptide fragment F1 of the peptide of the invention has a sequence selected from the group consisting of SEQ ID NO. 78-82.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid , and has sequence SEQ ID NO.10: (T)a(X 2 ) b D(X 4 ) c EG(X 6 ) d (X 7 ) e (X 8 ) f (Y) g wherein:
  • X 2 represents W, N, Q or K
  • X 4 represents P, N, a basic amino acid or a hydrophobic amino acid, preferably P, N, L, V, or A,
  • X 6 and X 7 are the same or different and represent A, V, L or I,
  • X 8 represents F or P
  • subindexes "a”, “b”, “c”, “d” “e”, “f” and “g” are integer numbers independently selected from 0 and 1 ; provided that two, three, four, five or six of the subindexes "a”, “b”, “c” “d”, “e”, “f' and “g” represent 1 ; and the remaining subindexes represent zero.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7-9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has SEQ ID NO. 10, wherein:
  • - X 6 and X 7 are the same or different and represent L, V, or A, and/or
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has SEQ ID NO. 83: (T)a(X 2 ) b D(X 4 )EG(X 6 ) d (X 7 ) e (X 8 ) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 , X 7 and X 8 are as defined in SEQ ID NO. 10 and X 4 represents P, L or N.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has SEQ ID NO. 84: (T)a(X 2 ) b DPEG(X 6 ) d (X 7 ) e (X 8 ) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 , X 7 and X 8 are as defined in SEQ ID NO. 10.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has a SEQ ID NO. 85: (T)a(X 2 ) b DLEG(X 6 ) d (X 7 ) e (X 8 ) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 , X 7 and X 8 are as defined in SEQ ID NO. 10.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has SEQ ID NO. 86: (T)a(X 2 ) b DNEG(X 6 ) d (X 7 ) e (X 8 ) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 , X 7 and X 8 are as defined in SEQ ID NO. 10.
  • fragment F1 of the peptide of the invention has a sequence selected from the group consisting of SEQ ID NO. 67-76
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid , and has sequence SEQ ID NO.11 : (T) a (X 2 ) b D(X 4 )EG(X 6 ) d (X 7 ) e (F)f(Y) g wherein:
  • X 2 represents W, N, Q or K
  • X 4 represents P, N or a basic amino acid
  • X 6 and X 7 are the same or different and represent A, V, L or I, subindexes "a”, “b”, “d”, “e”, “f”, and “g” are integer numbers independently selected from 0 and 1; provided that one, two, three, four or five of the subindexes "a”, “b”, “d” “e”, “f, and “g” represent 1 ; and the remaining subindexes represent zero.
  • peptide fragment F1 is as defined in the embodiment above, wherein:
  • X 2 represents W or N
  • X 4 represents P or N, and/or
  • X 6 or X 7 represents V, L or I .
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has a SEQ ID NO. 87: (T)a(X 2 ) b D(X 4 )EG(X 6 ) d (X 7 ) e (F) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 and X 7 are as defined in SEQ ID NO. 11 and X 4 represents P, L or N.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has SEQ ID NO. 88: (T)a(X 2 ) b DPEG(X 6 ) d (X 7 ) e (F) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 and X 7 are as defined in SEQ ID NO. 11.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has a SEQ ID NO. 89: (T)a(X 2 ) b DNEG(X 6 ) d (X 7 ) e (F) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 , X 7 and X 8 are as defined in SEQ ID NO. 11.
  • the peptide fragment F1 of the peptide of the invention has a length of 5-9, 6-9, 7- 9, 8-9, or 9 amino acids, particularly 5-9 amino acids, each one of the amino acids being L- or D-amino acid, and has a SEQ ID NO. 90: (T)a(X 2 ) b DLEG(X 6 ) d (X 7 ) e (F) f (Y) g , wherein a, b, d, e, f, g, X 2 , X 6 , X 7 and X 8 are as defined in SEQ ID NO. 11.
  • the peptide fragment F1 of the peptide of the invention has a sequence selected from the group consisting of: SEQ ID NO. 23-63.
  • the peptide of the invention wherein fragment F1 has a sequence selected from the group consisting of SEQ ID NO. 10, 11 , 83-90, 23-63, 67-76 has a length of 10-48, 11-48, 12-48, 13-48, 14-48, 15-48, 16-48, 17-48, 18-48, 18-48, 19-48, 20-48 amino acids, more particularly, 10-48 amino acids.
  • peptide fragment F1 has SEQ ID NO. 9: TWDPEGVIFY or is a sequence variant thereof that has at least 70% sequence identity with SEQ ID NO.9, wherein each one of the amino acids of peptide fragment F1 is a L- or D-amino acid.
  • peptide fragment F1 is a sequence variant of SEQ ID NO. 9 that has at least 80% sequence identity with SEQ ID NO.9, wherein each one of the amino acids of peptide fragment F1 is a L- or D-amino acid.
  • peptide fragment F1 is a sequence variant of SEQ ID NO. 9 that has at least 90% sequence identity with SEQ ID NO.9, wherein each one of the amino acids of peptide fragment F1 is a L- or D-amino acid.
  • sequence variant is defined below.
  • sequence variant in the context of variants of a peptide fragment with a specific sequence, substantially maintains or improves the activities of the reference peptide fragment from which it derives in the peptide of the invention.
  • the peptide of the invention that comprises a sequence variant of a peptide fragment substantially maintains or improves the activity of the peptide reference, wherein the peptide reference has the same sequence as the former, except that it comprises the reference peptide fragment, instead of the sequence variant thereof.
  • the peptide of the invention wherein fragment F1 is a sequence variant of SEQ ID NO.9 substantially maintains or improves the activity of the same peptide comprising instead of F1 as a sequence variant of SEQ ID NO.9, F1 with SEQ ID NO.9.
  • the sequence variant of said peptide fragment has at least 90 %, more particularly at least 95 %, or even more particularly at least 99% of the activity of the reference peptide fragment in the peptide of the invention or when part of the peptide of the invention.
  • the peptide of the invention that comprises a sequence variant of a peptide fragment has at least 90 %, more particularly at least 95 %, or even more particularly at least 99% of the activity of the peptide reference, wherein the peptide reference has the same sequence as the former, except that it comprises the reference peptide fragment, instead of the sequence variant thereof.
  • the activity of the peptide fragment or of the peptide of the invention refers to the lipolytic, anti-lipogenic, antifibrotic and/or anti-inflammatory activities of the peptide fragment or peptide, respectively.
  • it refers to the anti-lipogenic activity.
  • it refers to the anti-lipogenic and antifibrotic activities.
  • it refers to the anti-lipogenic and lipolytic activities.
  • it refers to the anti-lipogenic and anti-inflammatory activities.
  • it refers to the anti- lipogenic, antifibrotic and lipolytic activities.
  • it refers to the anti-lipogenic, antifibrotic and anti-inflammatory activities.
  • it refers to the anti-lipogenic, lipolytic and anti-inflammatory activities. In another particular embodiment, it refers to the anti-lipogenic, antifibrotic, lipolytic and anti-inflammatory activities. In another particular embodiment, it refers to the antifibrotic activity. In another particular embodiment, it refers to the antifibrotic and lipolytic. In another particular embodiment, it refers to the antifibrotic and anti-inflammatory activities. In another particular embodiment, it refers to the antifibrotic, lipolytic and anti-inflammatory activities. In another particular embodiment, it refers to the lipolytic activity. In another particular embodiment, it refers to the antiinflammatory activity. In another particular embodiment, it refers to the lipolytic and anti-inflammatory activities. Particularly, it refers to the anti-lipogenic or antifibrotic activity. More particularly, it refers to the anti-lipogenic and antifibrotic activity.
  • Methods to determine the activity of the peptide of the invention in particular the lipolytic, anti-lipogenic, antifibrotic and anti-inflammatory activities of a peptide, are provided below and apply herein.
  • methods to determine if a peptide fragment of interest maintains the activity of the reference peptide fragment in the peptide of the invention comprise comparing the corresponding activity of the peptide of the invention comprising the peptide fragment of interest, with that of the same peptide, comprising instead of the peptide fragment of interest, the reference peptide fragment.
  • peptide fragment F1 of the peptide of the invention has sequence SEQ ID NO.
  • TWDPEGVIFY wherein each one of the amino acids is L- or D-amino acid.
  • the peptide of the invention comprising SEQ ID NO. 9 as fragment F1 , has a length of 14-48 amino acids.
  • the peptide fragment F2 has a length of 5 to 19 amino acids, each one of the amino acids being L- or D-amino acid, and comprises sequence SEQ ID NO.2 (SF(X 9 )VR), wherein X 9 represents E or Q.
  • the peptide fragment F2 consists of sequence SEQ ID NO.2 (SF(X 9 )VR), wherein X 9 represents E or Q wherein each one of the amino acids is L- or D-amino acid.
  • the peptide fragment F2 comprises sequence SEQ ID NO. 12 (SFEVR). In another particular embodiment of the peptide or pharmaceutically acceptable salt thereof of the invention, the peptide fragment F2 consists of sequence SEQ ID NO. 12 (SFEVR).
  • the peptide fragment F2 of the peptide of the invention has SEQ ID NO. 13 (TKTSSSFEVR) or is a sequence variant thereof with at least 70% sequence identity with SEQ ID NO.13. In another particular embodiment, the peptide fragment F2 is a sequence variant thereof with at least 80% sequence identity with SEQ ID NO.13. In another particular embodiment, the peptide fragment F2 is a sequence variant thereof with at least 90% sequence identity with SEQ ID NO.13.
  • the peptide fragment F2 of the peptide of the invention has SEQ ID NO. 14 (VMTFDLTKITKTSSSFEVR) or is a sequence variant thereof with at least 70% sequence identity with SEQ ID NO.14. In another particular embodiment, the peptide fragment F2 is a sequence variant thereof with at least 80% sequence identity with SEQ ID NO.14. In another particular embodiment, the peptide fragment F2 is a sequence variant thereof with at least 90% sequence identity with SEQ ID NO.14.
  • sequence variant of a peptide fragment has been defined above in the context of fragment F1 and also applies herein.
  • the peptide of the invention wherein fragment F2 is a sequence variant of SEQ ID NO.13 substantially maintains or improves the activity of the same peptide comprising instead of F1 as a sequence variant of SEQ ID NO.13, F1 with SEQ ID NO.13.
  • the peptide of the invention wherein fragment F2 is a sequence variant of SEQ ID NO.14 substantially maintains or improves the activity of the same peptide comprising instead of F2 as a sequence variant of SEQ ID NO.14, F2 with SEQ ID NO.14.
  • the peptide fragment F2 of the peptide of the invention comprises SEQ ID NO. 13 (TKTSSSFEVR). In another embodiment, the peptide fragment F2 of the peptide of the invention consists of SEQ ID NO. 13 (TKTSSSFEVR). In another embodiment, the peptide fragment F2 of the peptide of the invention comprises SEQ ID NO. 14 (VMTFDLTKITKTSSSFEVR). In another embodiment, the peptide fragment F2 of the peptide of the invention consists of SEQ ID NO. 14 (VMTFDLTKITKTSSSFEVR). In an embodiment of the peptide of the invention, the peptide fragment F3 has a length of 10 to 20 amino acids and comprises SEQ ID NO. 4 (GDTNPKDDWF).
  • the peptide fragment F3 of the peptide of the invention comprises SEQ ID NO. 4 (GDTNPKDDWF). In an embodiment, the peptide fragment F3 of the peptide of the invention consists of SEQ ID NO. 4 (GDTNPKDDWF).
  • the peptide fragment F3 has SEQ ID NO. 4 (GDTNPKDDWF) or is a sequence variant thereof with at least 70% sequence identity with SEQ ID NO.4. In another particular embodiment of the peptide of the invention, the peptide fragment F3 is a sequence variant thereof with at least 80% sequence identity with SEQ ID NO.4. In another particular embodiment of the peptide of the invention, the peptide fragment F3 is a sequence variant thereof with at least 90% sequence identity with SEQ ID NO.4.
  • the peptide fragment F3 of the peptide of the invention comprises SEQ ID NO. 15 (GDTNPKDDWFMLGLRDGRPE). In another embodiment, the peptide fragment F3 of the peptide of the invention consists of SEQ ID NO. 15 (GDTNPKDDWFMLGLRDGRPE).
  • the peptide fragment F3 has SEQ ID NO. 15 (GDTNPKDDWF) or is a sequence variant thereof with at least 70% sequence identity with SEQ ID NO.15. In another particular embodiment of the peptide of the invention, the peptide fragment F3 is a sequence variant thereof with at least 80% sequence identity with SEQ ID NO.15. In another particular embodiment of the peptide of the invention, the peptide fragment F3 is a sequence variant thereof with at least 90% sequence identity with SEQ ID NO.15.
  • sequence variant of a peptide fragment has been defined above in the context of fragment F1 and also applies herein.
  • the peptide fragment F3 referred in any of the embodiment herein that is a variant of SEQ ID NO. 4 substantially maintains or improves the activities of peptide fragment F3 with SEQ ID NO.4 in the peptide of the invention.
  • the peptide of the invention wherein fragment F3 is a sequence variant of SEQ ID NO.4 substantially maintains or improves the activity of the same peptide comprising instead of F3 as a sequence variant of SEQ ID NO.4, F3 with SEQ ID NO.4.
  • the peptide of the invention wherein fragment F3 is a sequence variant of SEQ ID NO.15 substantially maintains or improves the activity of the same peptide comprising instead of F3 as a sequence variant of SEQ ID NO.15, F3 with SEQ ID NO.15.
  • the peptide fragment F1 is SEQ ID NO. 9 (TWDPEGVIFY)
  • the peptide fragment F2 is SEQ ID NO.
  • the peptide fragment F1 is SEQ ID NO. 9 (TWDPEGVIFY), the peptide fragment F2 is SEQ ID NO. 13 (TKTSSSFEVR) and the peptide fragment F3 is SEQ ID NO. 4 (GDTNPKDDWF).
  • the peptide fragment F1 is SEQ ID NO. 9 (TWDPEGVIFY) and the peptide fragment F2 is SEQ ID NO. 13 (TKTSSSFEVR).
  • the peptide fragment F1 is SEQ ID NO. 9 (TWDPEGVIFY) and the peptide fragment F2 is SEQ ID NO. 13 (TKTSSSFEVR).
  • the peptide fragment F1 is SEQ ID NO. 9 (TWDPEGVIFY) and the peptide fragment F3 is SEQ ID NO. 4 (GDTNPKDDWF).
  • the peptide of the inventions has sequence SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19
  • the peptide of the inventions has a length of 20- 30 amino acids and sequence SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • SEQ ID NO. 16 TKTSSSFEVRTWDPEGVIFY
  • SEQ ID NO. 17 TWDPEGVIFYGDTNPKDDWF
  • SEQ ID NO. 18 TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF
  • SEQ ID NO. 19 TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE
  • SEQ ID NO. 20 VMTFDLTKITKTSSSFEVRTWDPEGVIFY
  • the peptide of the invention has sequence SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVI FY).
  • the peptide of the inventions has a sequence that is a variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), that is at least 70%, 75%, 85%, 85%, particularly at least 70% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO.
  • TWDPEGVIFYGDTNPKDDWF SEQ ID NO. 18
  • SEQ ID NO. 19 TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE
  • SEQ ID NO. 20 VMTFDLTKITKTSSSFEVRTWDPEGVIFY
  • the peptide of the inventions has a sequence that is a sequence variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), and that is at least 70% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO.
  • TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • the peptide of the inventions has a sequence that is a sequence variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), and that is at least 75% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO.
  • TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • the peptide of the inventions has a sequence that is a sequence variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), and that is at least 80% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO.
  • TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • the peptide of the inventions has a sequence that is a sequence variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), and that is at least 85% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO.
  • TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • the peptide of the invention is a peptide with SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY) or a variant thereof at least 70%, 75%, 80%, 85%, particularly at least 90% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY).
  • the peptide of the invention is a peptide with SEQ ID NO. 180 (ATKTSASFEVRTWDPEAVIFY), wherein each one of the amino acids is a L- or D-amino acid.
  • the peptide of the invention is a peptide with SEQ ID NO. 181 (TKTASAFEVRTWDPEGVIFYGDTNPKDDWF), wherein each one of the amino acids is a L- or D-amino acid.
  • the peptide of the invention is a peptide with SEQ ID NO. 182 (TKTASAFEVRTWDPEGVIFY), wherein each one of the amino acids is a L- or D-amino acid.
  • the peptide of the invention is a peptide with SEQ ID NO. 183 (TKTSASFEVRTWDPEGVIFYADTNPKDDWF), wherein each one of the amino acids is a L- or D-amino acid.
  • the peptide of the inventions has a sequence that is a variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), , that is at least 90%, 92%, 95%, 97%, particularly at least 90% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO.
  • TWDPEGVIFYGDTNPKDDWF SEQ ID NO. 18
  • SEQ ID NO. 19 TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE
  • SEQ ID NO. 20 VMTFDLTKITKTSSSFEVRTWDPEGVIFY
  • the peptide of the inventions has a sequence that is a sequence variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), and that is at least 92% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO.
  • TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • the peptide of the inventions has a sequence that is a sequence variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY), and that is at least 95% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO.
  • the peptide of the inventions has a sequence that is a sequence variant of SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO.
  • VMTFDLTKITKTSSSFEVRTWDPEGVIFY and that is at least 97% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • the peptide of the invention is a peptide with SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY) or a variant thereof at least 90%, 92%, 95%, 97%, particularly at least 90% identical to SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY).
  • amino acid sequence modifications are well understood to those of skill in the art and can involve amino acid sequence modifications.
  • amino acid sequence modifications typically fall into one or more of three classes: substitutional, insertional, or deletional variants.ln a particular embodiment, the sequence modifications consist in the substitution of at least one amino acid or the reference amino acid sequence to an Alanine.
  • a gap i.e., a position in an alignment where a residue is present in one sequence but not in the other, is regarded as a position with non-identical residues and is counted as a compared position.
  • sequence identity between two amino acid sequences is preferably determined using algorithms based on global alignment, such as the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, J. Mol. Biol. 48: 443-453), preferably implemented in the Needle program of the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al., 2000, Trends Genet. 16: 276-277); or the BLAST Global Alignment tool (Altschul et al., "Basic local alignment search tool”, 1990, J. Mol. Biol, v.
  • the variant thereof substantially maintains or improves the lipolytic, anti- lipogenic, antifibrotic and anti-inflammatory activities of the reference peptide from which it derives.
  • substantially maintains or improves the lipolytic, anti-lipogenic, antifibrotic and anti-inflammatory activities is meant that the variant thereof has at least 90 %, more particularly at least 95 %, or even more particularly at least 99% of the lipolytic, anti-lipogenic, antifibrotic and anti-inflammatory activities of the reference peptide.
  • the peptide fragment F2 has a length of 5-10, 6-10, 7-10,
  • amino acids 8-10, 9-10 or 10 amino acids, particularly 5-10 amino acids, each one of the amino acids being L- or D- amino acid and has sequence:
  • X 1 represents T or A
  • X 2 represents K or A,.
  • X 3 represents T or A
  • X 4 represents S or A
  • X 5 represents S or A
  • X 6 represents E or Q, and subindexes a, b, c, d, and e are integer numbers independently selected from 0 and 1.
  • fragment F2 has a sequence selected from the list consisting of: SEQ ID NO. 13, 92-106.
  • the peptide fragment F1 has a length of 7-10, 8-10,
  • amino acids 9-10, or 10 amino acids, particularly 7-10 amino acids, each one of the amino acids being L- or D-amino acid and has sequence
  • X 1 represents T, or A
  • X 2 represents W, N, or A
  • X 3 represents D or N
  • X 4 represents P, or L
  • X 5 represents E or Q
  • X 7 represents L or I, and subindexes a, c, d and f are integer numbers independently selected from 0 and 1.
  • the peptide fragment F1 has a sequence selected from the group consisting of SEQ ID NO. 109-124, 107 and 179.
  • the peptide of the invention has a length of 9-49, 12-35, 15-30, 15- 20 amino acids, in particular 15-20 amino acids amino acids and comprises:
  • X 1 represents T, or A
  • X 2 represents W, N, or A
  • X 3 represents D or N
  • X 4 represents P, or L
  • X 5 represents E or Q
  • X 7 represents L or I, and subindexes a, c, d and f are integer numbers independently selected from 0 and 1, and
  • a peptide fragment F2 with a length of 5-10, 6-10, 7-10, 8-10, 9-10 or 10 amino acids amino acids, each one of the amino acids being L- or D-amino acid, and with sequence
  • X 1 represents T or A
  • X 2 represents K or A,.
  • X 3 represents T or A
  • X 4 represents S or A
  • X 5 represents S or A
  • X 6 represents E or Q, and subindexes a, b, c, d, and e are integer numbers independently selected from 0 and 1.
  • the peptide of the invention has a sequence selected from the group consisting of SEQ ID NO. 127-161.
  • peptide fragment F2 has a sequence selected from the group consisting of SEQ ID NO. 91 , 13, 92-106, wherein at least one of the amino acids of the fragment is a D-amino acids. In a more particular embodiment, peptide fragment F2 has a sequence selected from the group consisting of SEQ ID NO. 91 , 13, 92-106, wherein all the amino acids of the fragment are D-amino acids. In another particular embodiment of the peptide of the invention, peptide fragment F1 has a sequence selected from the group consisting of SEQ ID NO. 107-124, 179 wherein at least one of the amino acids of the fragment is a D-amino acids. In a more particular embodiment, peptide fragment F1 has a sequence selected from the group consisting of SEQ ID NO. 107-124, 179, wherein all the amino acids of the fragment are D-amino acids.
  • the peptide of the invention comprises peptide fragments F1 , F2 and F3. In another embodiment, the peptide of the invention comprises peptide fragments F1 and F2. In another embodiment, the peptide of the invention comprises peptide fragments F1 and F3.
  • the peptide of the invention does not comprise fragment F2. In another embodiment, the peptide of the invention does not comprise peptide fragment F3.
  • the peptide of the invention consists of peptide fragments F1, F2 and F3. In another embodiment, the peptide of the invention consists of peptide fragments F1 and F2. In another embodiment, the peptide of the invention consists of peptide fragments F1 and F3.
  • each one of the amino acids of the peptide of the invention is an L- or a D-amino acid.
  • the peptide of the invention comprises at least 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , 12, 13, 14, 15, 16,1 7, 18, 19, 20, 21 , 22, 23, 24, 25,26, 27,28, 29, 30, 31 , 32, 33, 34, 35, 36, 37, 38, 39, 40, 41 , 42, 43, 44, 45, 46, 47, 48, preferably at least 1 D-amino acid and the rest of amino acids are L-amino acids.
  • the peptide of the invention comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , 12, 13, 14, 15, 16,1 7, 18, 19, 20, 21 , 22, 23, 24, 25,26, 27,28, 29, 30, 31 , 32, 33, 34, 35, 36, 37, 38, 39, 40, 41 , 42, 43, 44, 45, 46, 47, 48, particularly 1 D-amino acid and the rest of amino acids are L-amino acids.
  • all the amino acids of the peptide of the invention are D-amino acids.
  • all the amino acids of the peptide of the invention are L-amino acids.
  • each one of the amino acids of peptide fragment F1 as defined herein is an L- or a D-amino acid.
  • peptide fragment F1 as defined herein comprises at least one, 2, 3, 4, 5, 6, 7, 8, 9, particularly at least 1 D-amino acid, and the rest of amino acids of the peptide fragment are L-amino acids.
  • peptide fragment F1 as defined herein comprises 1 , 2, 3, 4, 5, 6, 7, 8, 9, particularly 1 D-amino acid, and the rest of amino acids of the peptide fragment are L-amino acids.
  • all the amino acids of the peptide fragment F1 as defined herein are D-amino acids.
  • all the amnio acids of peptide fragment F1 are L-amino acids.
  • each one of the amino acids of peptide fragment F2 as defined herein is an L- or a D-amino acid.
  • peptide fragment F2 as defined herein comprises at least one, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , 12, 13, 14, 15, 16, 17or 18, particularly at least 1 D-amino acid, and the rest of amino acids of the peptide fragment are L-amino acids.
  • peptide fragment F2 as defined herein comprises 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17,18, particularly 1 D-amino acid, and the rest of amino acids of the peptide fragment are L-amino acids.
  • all the amino acids of the peptide fragment F2 as defined herein are D-amino acids.
  • all the amino acids of peptide fragment F2 are L-amino acids.
  • each one of the amino acids of peptide fragment F3 as defined herein is an L- or a D-amino acid.
  • peptide fragment F3 as defined herein comprises at least one, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , 12, 13, 14, 15, 16, 17, 18 or 19, particularly at least 1 D-amino acid, and the rest of amino acids of the peptide fragment are L-amino acids.
  • peptide fragment F2 as defined herein comprises 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , 12, 13, 14, 15, 16, 17, 18 or19, particularly 1 D- amino acid, and the rest of amino acids of the peptide fragment are L-amino acids.
  • all the amino acids of the peptide fragment F3 as defined herein are D-amino acids.
  • all the amino acids of peptide fragment F3 are L-amino acids.
  • the peptide comprises F2, F1 and F3, and each one of the amino acids of peptide fragments F2 and F3 is an L- or a D-amino acid and all amino acids in fragment Fl are L-amino acids, preferably wherein fragment F1 has sequence SEQ ID NO.9 or SEQ ID NO.124.
  • the peptide comprises F2, F1 and F3, and at least one amino acid is a D-amino acid in fragments F2 and F3, and all amino acids are L-amino acids in fragment F1 , preferably wherein fragment F1 has sequence SEQ ID NO.9 or SEQ ID NO.124.
  • the peptide comprises F2 and F3, and all amino acid are a D-amino acid in fragments F2 and F3, and all amino acids are L-amino acids in fragment F1 , preferably wherein fragment F1 has sequence SEQ ID NO.9 or SEQ ID NO.124.
  • the peptide comprises fragments F2 and F1 , and each one of the amino acids of peptide in fragments F2 is an L- or a D- amino acid, and all amino acids in fragment F1 , preferably wherein fragment F1 are L-amino acids, preferably wherein fragment F1 has sequence SEQ ID NO.9 or SEQ ID NO.124.
  • the peptide comprises fragments F2 and F1 and at least one amino acid is a D-amino acid in fragment F2, and all amino acids are L-amino acids in fragment F1 , preferably wherein fragment F1 has sequence SEQ ID NO.9 or SEQ ID NO.124.
  • the peptide comprises fragments F2 and F1 , and all amino acid are a D-amino acid in fragment F2, and all amino acids are L-amino acids in fragment F1 , preferably wherein fragment F1 has sequence SEQ ID NO 9 or SEQ ID NO.124.
  • the peptide comprises fragments F3 and F1 , and each one of the amino acids of peptide in fragments F3 is an L- or a D- amino acid, and all amino acids are L-amino acids in fragment F1 , preferably wherein fragment F1 has sequence SEQ ID NO.9 or SEQ ID NO.124.
  • the peptide comprises fragments F3 and F1 and at least one amino acid is a D- amino acid in fragment F3, and all amino acids are L-amino acids in fragment F1 , preferably wherein fragment F1 has sequence SEQ ID NO 9 or SEQ ID NO.124.
  • the peptide comprises fragments F3 and F1, and all amino acid are a D-amino acid in fragment F3, and all amino acids are L-amino acids in fragment F1 , preferably wherein fragment F1 has sequence SEQ ID NO 9 or SEQ ID NO.124.
  • fragment F1 has SEQ ID NO. 1 , SEQ ID NO. 5, SEQ ID NO. 6, SEQ ID NO. 7, SEQ ID NO. 8, SEQ ID NO. 9, SEQ ID NO. 10 or SEQ ID NO. 11 , and at least one of the amino acids of the fragment is D-aa.
  • fragment F2 has SEQ ID NO. 2, 12, 13 or 14, and and at least one of the amino acids of the fragment is D-aa.
  • fragment F3 has SEQ ID NO. 4 or SEQ ID NO. 15 and at least one of the amino acids of the fragment is D-aa.
  • fragment F1 has SEQ ID NO. 1 , SEQ ID NO. 5, SEQ ID NO. 6, SEQ ID NO. 7, SEQ ID NO. 8, SEQ ID NO. 9, SEQ ID NO. 10 or SEQ ID NO. 11, and all the amino acids of the fragment are D-aa.
  • fragment F2 has SEQ ID NO. 2, 12, 13 or 14, and all the amino acids of the fragment are D-aa.
  • fragment F3 has SEQ ID NO. 4 or SEQ ID NO. 15 and all the amino acids of the fragment are D-aa.
  • D amino acid refers to an amino acid having a D configuration, well known by an expert in the field.
  • L amino acid refers to an amino acid having an L configuration, well known by an expert in the field.
  • the one or more of the amino acids forming the peptide fragments or the peptide of the invention can have an L- or D-configuration.
  • At least one amino acid of the peptide of the invention comprises a modification in its side chain.
  • said modification is the addition of a -C(O)Rz group to the side chain of the peptide, being Rz a (Ci-C2o)alkyl or a (Ci-C2o)alkenyl.
  • Rz is (Ci-C2o)alkyl.
  • the modification is the addition of an acetyl group or a palmitoyl group.
  • the modification is the addition of a -C(O)Rz group to the side chain of the peptide , being Rz a (Ci-C2o)alkenyl .
  • the amino acid is a lysine or a tryptophane.
  • the modified amino acid is not at the N- nor in the C- terminal end position of the peptide.
  • the modified amino acid is the lysine in fragment F2 with SEQ ID NO. 13 (TKTSSSFEVR).
  • the modified amino acid is the lysine in fragment F2 with SEQ ID NO. 13 (TKTSSSFEVR) and consists in the addition of an acetyl group.
  • the modified amino acid is lysine in fragment F2 with SEQ ID NO. 13 (TKTSSSFEVR) and consists in the addition of a palmitoyl group.
  • the modified amino acid is the tryptophane in fragment F1 with SEQ ID NO. 9: TWDPEGVIFY.
  • the modified amino acid is the tryptophane in fragment F1 with SEQ ID NO. 9: TWDPEGVIFY and consists in the addition of a palmitoyl group.
  • At least one amino acid of the peptide fragment as defined in any of the embodiments in the present paragraph is a D-amino acid, even yet more particularly, all the amio acids of said fragment are a D-amino acid.
  • the N-terminal end of the peptide of the invention corresponds to — NR1R2, being R1 and R2 independently selected from the group consisting of -H, -C(0)R3, a triglyceride, (Ci-C2o)alkyl, particularly (Ci-Ci5)alkyl, more particularly (Ci-Cio)alkyl and (Ci-C2o)alkenyl, particularly (Ci-Ci5)alkenyl, more particularly (Ci-Cio)alkenyl.
  • the N-terminal end of the peptide of the invention corresponds to — NR1R2, being R1 and R2 independently selected from the group consisting of -H, -C(0)R3, a triglyceride, (Ci-C2o)alkyl, (Ci-Ci5)alkyl, (Ci-Cio)alkyl, (Ci-C2o)alkenyl, (Ci-Ci5)alkenyl, and (Ci-Cio)alkenyl.
  • the N terminal end of the peptide of the invention corresponds to NH2 or -NHC(O)R3, being R3 a (Ci-C2o)alkyl, particularly being R3 a (Ci-Ci5)alkyl, more particularly being R3 a (Ci-Cio)alkyl.
  • the N terminal end of the peptide of the invention corresponds to NH2.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3, being R3 a (Ci- C2o)alkyl, preferably being R3 a (Ci-Ci5)alkyl, more preferably being R3 a (Ci-Cio)alkyl.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3, being R3 a (Ci-C2o)alkenyl, particularly being R3 a (Ci-Ci5)alkenyl, more particularly being R3 a (Ci-Cio)alkenyl.
  • the N terminal end of the peptide of the invention corresponds to - NHC(O)R3 and R3 is -CH3. In another particular embodiment, the N terminal end of the peptide of the invention corresponds to -NHC(O)R3 and R3 is CH3CH2. In another particular embodiment, the N terminal end of the peptide of the invention corresponds to -NHC(O)R3 and R3 is CH3(CH2)i4.
  • the C-terminal end of the peptide is -COOH, -C(O)NH2 or -C(O)NHR6, wherein Re is (Ci-C2o)alkyl or (Ci-C2o)alkenyl.
  • the C-terminal end of the peptide is -COOH or C(O)NH2.
  • the N terminal end of the peptide of the invention corresponds to NH2 or -NHC(O)R3, being Rsa (Ci-Cio)alkyl; and the C-terminal end of the peptide is -COOH or -C(O)NH 2 .
  • the N terminal end of the peptide of the invention corresponds to -NHC(0)R3, being R3 a (Ci-Cio)alkenyl; and the C-terminal end of the peptide is -COOH or -C(O)NH 2 .
  • the N terminal end of the peptide of the invention corresponds to NH2; and the C- terminal end of the peptide is -COOH, -C(O)NH2 or -C(O)NHRe, wherein Re is (Ci-C2o)alkyl, preferably wherein the C-terminal end of the peptide is -COOH or C(O)NH2.
  • the N terminal end of the peptide of the invention corresponds to NH2; and the C-terminal end of the peptide is-C(0)NHR6, wherein Re is (Ci-C2o)alkenyl.
  • the N terminal end of the peptide of the invention corresponds to -NHC(0)R3, being R3 a (Ci-C2o)alkyl, preferably being R3 a (Ci-Ci5)alkyl, more preferably being R3 a (Ci-Cio)alkyl; and the C-terminal end of the peptide is - COOH, -C(O)NH2 or -C(O)NHR6, wherein Re is (C1-C20) alkyl, preferably wherein the C-terminal end of the peptide is -COOH or C(O)NH2.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3, being Rs a (Ci-C2o)alkenyl, preferably being R3 a (Ci-Ci5)alkenyl, more preferably being R3 a (Ci-Cio)alkenyl; and the C-terminal end of the peptide is - COOH, -C(O)NH2 or -C(O)NHR6, wherein Re is (Ci-C2o)alkyl, preferably wherein the C-terminal end of the peptide is -COOH or C(O)NH2.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3, being R3 a (Ci-C2o)alkenyl, preferably being R3 a (Ci-Ci5)alkenyl, more preferably being R3 a (Ci-Cio)alkenyl; and the C-terminal end of the peptide is -C(O)NHR6, wherein Re is (Ci-C2o)alkenyl.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3 and R3 is -CH3; and the C-terminal end of the peptide is - COOH, -C(O)NH2 or - C(O)NHRe, wherein Re is (Ci-C2o)alkyl, preferably wherein the C-terminal end of the peptide is -COOH or C(O)NH 2 .
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3 and R3 is -CH3; and the C-terminal end of the peptide is -C(O)NHRe, wherein R6 is (Ci-C2o)alkenyl.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3 and R3 is CH3CH2; and the C-terminal end of the peptide is - COOH, -C(O)NH2 or -C(O)NHRe, wherein R6 is (Ci-C2o)alkyl, preferably wherein the C-terminal end of the peptide is -COOH or C(O)NH 2 .
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3 and R3 is CH3CH2; and the C-terminal end of the peptide is -C(O)NHRe, wherein R6 is (Ci-C2o)alkenyl.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3, being R3 CH3(CH2)i4; and the C-terminal end of the peptide is - COOH, -C(O)NH2 or -C(O)NHRe, wherein Re is (C1-C20) alkyl, preferably wherein the C-terminal end of the peptide is -COOH or C(O)NH2.
  • the N terminal end of the peptide of the invention corresponds to -NHC(O)R3, being R3 CH3(CH2)i4; and the C-terminal end of the peptide is -C(O)NHRe, wherein Re is (Ci-C2o)alkenyl.
  • (Ci-C2o)alkyl refers to a saturated straight or branched alkyl chain having from 1 to 20 carbon atoms.
  • the terms (Ci-Cie)alkyl and (Ci-Cio)alkyl refer to saturated straight or branched alkyl chains having each from 1 to 15 carbon atoms, or 1 to 10 carbon atoms, respectively.
  • (Ci-C2o)alkeny I refers to mono- or poly-unsaturated straight or branched alkenyl chain having from 1 to 20 carbon atoms.
  • the terms (Ci-Cie)alkenyl and (Ci-Cio)alkenyl refer to mono- or polyunsaturated straight or branched alkenyl chains having each from 1 to 15 carbon atoms, or 1 to 10 carbon atoms, respectively.
  • the peptide of the invention has lipolytic activity.
  • lipolytic activity refers to the activity consisting in inducing lipolysis.
  • a peptide with lipolytic activity refers to a peptide that induces lipolysis, in particular when administered to an animal body.
  • lipolysis is the enzymatic decomposition of triglycerides into glycerol and fatty acids. Methods to determine the lipolytic activity of a peptide as just defined are well-known by an expert in the field and include those disclosed in the examples of the present invention, such as in example 2-4 or 6.
  • Non-limitative examples of such methods include adding the peptide of interest, optionally at different concentrations of for instance 1 pig/ml, 10 pig/ml, 25 pig/ml , 50 pig/ml , 75 pig/ml or 100 pig/ml, to a cell culture of differentiated adipocytes, such as mouse adipocytes, for instance differentiated 3T3-L1 cell line mouse adipocytes (Ref. JCRB9014-A) from Tebu-Bio (Tebu-bio, Barcelona, Spain) or human mature adipocytes.
  • differentiated adipocytes such as mouse adipocytes, for instance differentiated 3T3-L1 cell line mouse adipocytes (Ref. JCRB9014-A) from Tebu-Bio (Tebu-bio, Barcelona, Spain) or human mature adipocytes.
  • a control compound is added to another cell culture of the same cell type at the same or comparable concentration as the peptide of interest has been added
  • the supernatant of both cell cultures is collected (that with the peptide of interest and that with the control compound), and the glycerol content present in each supernatant is determined, with for instance Lipolysis Assay kit from Tebu-bio (LIP-1-NC).
  • the amount of glycerol detected is considered to be the glycerol released by the cultured cells in the presence of the corresponding compound. If the amount of glycerol released by the cells cultured in the presence of the peptide of interest is equal or higher than that released by the cell cultured in the presence of the control compound, it is considered that the peptide of interest has lipolytic activity, in particular equal or higher than that of the control compound.
  • control compound is isoproterenol or semaglutide.
  • isoproterenol refers to the compound with lUPAc name 4-[1-hydroxy-2-(propan- 2-ylamino)ethyl]benzene-1 ,2-diol.
  • maglutide refers to the compound with CAS number 910463-68-2.
  • the peptide of the invention has lipolytic activity, wherein the lipolytic activity of the peptide is equal or higher than that of a control compound.
  • the control compound is is isoproterenol or semaglutide, particularly isoproterenol. ...
  • the peptide of the invention has a lipolytic activity that is equal to that of a control compound if it is higher or lower than that of the control compound in less than 30%, 25%, 20%, 15%, 12%, 10%, 7%, 5%, 3%, 1 % of that of a control compound.
  • the peptide of the invention has a lipolytic activity that is equal to that of a control compound if the lipolytic activity of the peptide is at least 70%, 75%, 80%, 85%, 90%, 95%, 100%, particularly at least 80% of the lipolytic activity of the control compound.
  • the peptide of the invention has a lipolytic activity higher than that of a control compound if it is at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 60%, 70%, 80%, 90%, 100%, 120%, 150%, 200%, 250%, 300%, 350%, 400%, 450%, 500%, 550%, 600%, particularly at least 30%, higher than that of said control compound.
  • the lipolytic activity as referred herein for the peptide of the invention is measured by a method that determines the amount of glycerol released by differentiated adipocytes in culture with a certain concentration of the peptide of the invention, such as 100pig/ml, for a period of time of 2h-16h, preferably 16 h, and compares said amount of glycerol released with that released by a cell culture of the same cell type in culture with the same amount of a control compound for the same amount of time, wherein if the amount of glycerol released by the cells in culture with the peptide of the invention is equal or higher than that released by the cells in culture with the control compound, the peptide is considered to have lipolytic activity.
  • a certain concentration of the peptide of the invention such as 100pig/ml
  • control compound is isoproterenol or semaglutide, particularly isoproterenol.
  • amount of glycerol released by the cells in culture with the peptide of the invention equal or higher than that released by the cells in culture with the control compound is any of the percentages indicated above for an equal or higher lipolytic activity of the peptide as compared to a control peptide, wherein the lipolytic activity is substituted by the amount of glycerol released by the corresponding cells.
  • the peptide of the invention has anti-lipogenic activity.
  • anti-lipogenic activity refers to the activity that consist in avoiding the formation of triglycerides from the enzymatic condensation of glycerol and fatty acids, in particular in an animal body.
  • a peptide with anti-lipogenic activity refers to a peptide that avoids, or inhibits, the formation of triglycerides from the enzymatic condensation of glycerol and fatty acids, in particular in an animal body.
  • a non-limitative example of a method to determine if a peptide has anti-lipogenic activity includes adding the peptide of interest, optionally at different concentrations of for instance 1 pig/ml, 10 pig/ml, 25 pig/ml , 50 pig/ml , 75 pig/ml or 100 pig/ml, to a cell culture of HepG2 cells treated with fructose to induce lipogenesis (such as 30mM of fructose).
  • a first control cell culture of HepG2 cells treated with fructose is also prepared, and a second control cell culture of HepG2 cells treated with fructose is also prepared in which a control compound is added at the same or comparable concentration as the peptide of interest has been added to the other cell culture.
  • the control compound can be for instance telmisartan or semaglutide.
  • the expression level, particularly in serum, of key proteins involved in lipogenesis, such as PPARy transcription factor, Acetyl-CoA carboxylase (ACC) enzymes is determined in the cells of each of the cell cultures.
  • the expression level of said enzyme/s is/are reduced in the cell culture in the presence of the peptide of the invention at an equal or higher level than in the cell culture in the presence of the control compound, as compared to in the first control cell culture, it is considered that the peptide has anti-lipogenic activity.
  • Methods to determine the expression level of specific proteins in the cells are well-known by an expert in the field and include RT-PCR, or RNA sequencing. Other methods include detection of the level of protein in the cells using specific antibodies against said protein, for instance in a western blot, ELISA or by mass spectrometry.
  • telmisartan refers to the compound with CAS number 144701-48-4.
  • the peptide of the invention has anti-lipogenic activity, wherein the anti-lipogenic activity of the peptide is equal or higher than that of a control compound.
  • the control compound is telmisartan or semaglutide, particularly selmaglutide.
  • the control compound is telmisartan.
  • the peptide of the invention has an anti-lipogenic activity that is equal to that of a control compound if it is higher or lower than that of said control compound in less than 30%, 25%, 20%, 15%, 12%, 10%, 7%, 5%, 3%, 1 % of that of a control compound.
  • the peptide of the invention has an anti-lipogenic activity that is equal to that of a control compound if the anti-lipogenic activity of the peptide is at least 70%, 75%, 80%, 85%, 90%, 95%, 100%, particularly at least 80% of the anti-lipogenic activity of the control compound.
  • the peptide of the invention has an anti-lipogenic activity higher than that of a control compound if it is at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 60%, 70%, 80%, 90%, 100%, 120%, 150%, 200%, 250%, 300%, 350%, 400%, 450%, 500%, 550%, 600%, 700%, 1000% preferably at least 50%, higher than that of said control compound.
  • Methods to determine the anti-lipogenic activity of a peptide or compound have been provided above in the definition of "anti-lipogenic activity”.
  • the anti-lipogenic activity as referred herein for the peptide of the invention is measured by a method that compares the expression level of anti-lipogenic proteins, such as PPARy, ACC and/or FAS in cells, particularly in HEPG2 cells in culture for 2-7 days, particularly 5 days, with a certain concentration of the peptide of the invention, such as 100pig/ml, and with induced lipogenesis, particularly by adding fructose, more particularly 30mM of fructose, into the cell culture, with the expression level of said protein/s in cells in culture with a control compound for the same amount of time with induced lipogenesis as well, wherein if the expression level and if the expression level of said proteins is lower in the cells in culture with the peptide of the invention than in in the cells in culture with the control compound, it is considered that the peptide of the invention has anti-lipogenic activity.
  • anti-lipogenic proteins such as PPARy, ACC and/or FAS in cells, particularly in HEPG2 cells in culture
  • Methods to determine the expression level of a protein in cells have been provided above in the definition of "anti-lipogenic activity”.
  • the peptide of the invention has antifibrotic activity.
  • antifibrotic refers to the activity consisting in reducing or inhibiting fibrosis.
  • Fibrosis is defined by the overgrowth, hardening, and/or scarring of various tissues and is attributed to excess deposition of extracellular matrix components including collagen. Repeated injuries, chronic inflammation and repair are susceptible to fibrosis, where an accidental excessive accumulation of extracellular matrix components, such as collagen, is produced by fibroblasts, leading to the formation of a permanent fibrotic scar. Indeed, fibrosis is a pathological feature of most chronic inflammatory diseases.
  • antifibrotic activity in the context of a compound or the peptide of the invention, refers to the capacity of said compound or peptide to reduce the formation of fibrous tissue, or the excess deposition of extracellular matrix components including collagen in a tissue.
  • the antifibrotic activity refers to the inhibition of the formation of the fibrotic tissue, or of the excess deposition of extracellular components, such as collagen. In another embodiment, the antifibrotic activity refers to the reduction in the amount of fibrotic tissue formed, or of the excessive extracellular components deposited, such as of collagen.
  • Non-limitative examples of said methods include determining, upon subcutaneous administration of the peptide of interest for a certain time (for instance 20mg/kg/day of the peptide of the invention during 10 weeks) to a mouse model of fibrosis (for instance a mouse model of fibrosis wherein fibrosis is induced by twice a week intraperitoneal injection of CCI4 (1 ml/Kg diluted in olive oil 1 :5) during a 4 weeks period), the expression level in serum of collagen.
  • a mouse model of fibrosis for instance a mouse model of fibrosis wherein fibrosis is induced by twice a week intraperitoneal injection of CCI4 (1 ml/Kg diluted in olive oil 1 :5) during a 4 weeks period
  • the expression level of collagen is reduced upon administration of the peptide as compared to the lack of administration of the peptide, or to the administration of a negative control (such as the vehicle used for the administration of the peptide), it is considered that the peptide has antifibrotic activity.
  • Methods to determine the expression level of specific proteins in the serum of mouse are well-known by an expert in the field and include determining the mRNA expression level in serum samples isolated from the treated and control mice by RT-PCR or RNA sequencing. Other methods include detection of the level of protein in serum using specific antibodies against said protein, for instance in a western blot, ELISA or by mass spectrometry.
  • Alternative or additional methods include comparing the collagen deposition in the fibrotic tissue formed in the fibrosis mouse model treated with the negative control (or not treated with the peptide of the invention), and the collagen deposited in the same tissue in the mouse treated with the peptide of interest. Histological studies using picrosirius staining (collagen staining) can be used for that purpose. If there is a reduction in the picrosirius staining intensity or in the picrosirius stained surface, it is considered that the peptide of the invention has antifibrotic activity.
  • the antifibrotic activity as referred herein for the peptide of the invention is measured by a method that compares the expression level of collagen in an isolated serum sample from a mouse model of fibrosis, particularly in a mouse with fibrosis induced fibrosis induced by injection of CCI4, particularly a twice a week intraperitoneal injection of CCI4 (1 ml/Kg diluted in olive oil 1 :5) during a 4 weeks period, and that has received subcutaneous administration of 20mg/kg/day of the peptide of the invention during 8 weeks to that in an isolated serum sample from a corresponding control mouse that has not received the peptide of the invention, or that has received a negative control (such as the vehicle used in the administration of the peptide of the invention), and if the expression level of collagen is lower in the serum sample of the mouse treated with the peptide of the invention than in the serum sample of the mouse not treated with the peptide of the invention (or treated with the negative control), it is considered that the peptide
  • the expression "expression level of collagen lower than”, as used herein, refers to an expression level that is at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 60%, 70%, 80%, 90%, 100%, 120%, 150%, 200%, 250%, 300%, 350%, 400%, 450%, 500%, 550%, 600%, preferably at least 20%, lower than the corresponding reference level.
  • Methods to determine the expression level of a protein in a serum sample have been provided above in the definition of "anti-lipogenic activity”.
  • the peptide of the invention has anti-inflammatory activity.
  • anti-inflammatory activity refers to the activity consisting in reducing inflammation or swelling in an animal body. Inflammation is part of the complex biological response of body tissues to harmful stimuli, such as damaged cells, irritants, or pathogens, and is a protective response involving immune cells, blood vessels, and molecular mediators. The five cardinal signs are heat, pain, redness, swelling, and loss of function.
  • the function of inflammation is to eliminate the initial cause of cell injury, clear out necrotic cells and tissues damaged from the original insult and the inflammatory process, and initiate tissue repair. Too little inflammation could lead to progressive tissue destruction by the harmful stimulus (e.g. bacteria) and compromise the survival of the organism. In contrast, too much inflammation, in the form of chronic inflammation, is associated with various diseases, such as hay fever, periodontal disease, atherosclerosis, and osteoarthritis.
  • a peptide with anti-inflammatory activity refers to a peptide that reduces an inflammatory response of the body, in particular, the inflammation signs in a part of the body, such as heat, pain, redness, swelling, and loss of function.
  • Methods to determine if a peptide has anti-inflammatory activity are well-known by an expert in the field and include those disclosed in the examples of the invention, such as in examples 4 or 6 of the present invention.
  • Non-limitative examples of such methods include determining, upon subcutaneous administration of the peptide of interest for a certain time (for instance 20mg/kg/day of the peptide of the invention during 10 weeks) to a mouse model of a disease that is associated to inflammation (such as of obesity or fatty liver disease, induced for instance by high fat diet feeding), the expression level in serum of protein markers of inflammation, such as F480.
  • a mouse model of a disease that is associated to inflammation such as of obesity or fatty liver disease, induced for instance by high fat diet feeding
  • the expression level in serum of protein markers of inflammation such as F480.
  • proinflammatory cytokines such as TNFo, IL1 p and/or IL6
  • adipose tissue inflammation is to be determined, the expression level of IL1 p, leptin and/or adiponectin are determined.
  • the expression level of said proteins is reduced, or the expression level of adiponectin is increased, upon administration of the peptide as compared to the lack of administration of the peptide, or to the administration of a negative control (such as the vehicle used for the administration of the peptide), it is considered that the peptide has anti-inflammatory activity.
  • Methods to determine the expression level of a protein in a serum sample have been provided above in the definition of anti-lipogenic activity.
  • the anti-inflammatory activity as referred herein for the peptide of the invention is measured by a method that compares the expression level of protein markers of inflammation, such as F480, TNFo, IL1 p, IL6, leptin and/or adiponectin, in an isolated serum sample from a mouse model of a diseases associated to inflammation, particularly obesity or fatty liver, more particularly induced by high fat diet feeding, that has received subcutaneous administration of 20mg/kg/day of the peptide of the invention during 8 weeks to that in an isolated serum sample from a corresponding control mouse that has not received the peptide of the invention, or that has received a negative control (such as the vehicle used in the administration of the peptide of the invention), and if the expression level of said protein F480, TNFo, IL1 p, IL6, and/or leptin is lower, and/or the expression level of adiponectin is higher, in the serum sample of the mouse treated with the peptide of the invention than in
  • the expression "expression level of said proteins lower than”, as used herein, refers to an expression level that is at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 60%, 70%, 80%, 90%, 100%, 120%, 150%, 200%, 250%, 300%, 350%, 400%, 450%, 500%, 550%, 600%, preferably at least 20%, lower than the corresponding reference level.
  • the expression "expression level of adiponectin is higher than”, as used herein, refers to an expression level that is at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 60%, 70%, 80%, 90%, 100%, 120%, 150%, 200%, 250%, 300%, 350%, 400%, 450%, 500%, 550%, 600%, preferably at least 20%, higher than the corresponding reference level.
  • Methods to determine the expression level of a protein in a serum sample have been provided above in the definition of "anti-lipogenic activity”.
  • the peptide of the invention has lipolytic activity, anti-lipogenic activity, anti- fibrotic and/or anti-inflammatory activity, as just defined. In a more particular embodiment, the peptide of the invention has lipolytic activity, anti-lipogenic activity, anti-fibrotic and/or anti-inflammatory activity. In another particular embodiment, the peptide of the invention has anti-lipogenic, anti-fibrotic and anti-inflammatory activity.
  • the peptide of the invention has a lipolytic activity equal or higher than that of a control compound, and anti-lipogenic activity equal or higher than a control compound.
  • the peptide of the invention has a lipolytic activity equal or higher than that of a control compound, wherein said control compound is isoproterenol or semaglutide, more particularly isoproterenol, and anti-lipogenic activity equal or higher than a control compound, wherein said control compound is telmisartan or semaglutide, more particularly semaglutide.
  • all the definitions and embodiments addressed to the peptide of the invention also apply to the pharmaceutically acceptable salt thereof as defined above, or the pharmaceutically acceptable salt of the peptide of the invention, or the pharmaceutically acceptable salt of the invention.
  • the invention in a second aspect, relates to a pharmaceutical composition
  • a pharmaceutical composition comprising a therapeutical effective amount of the peptide, or pharmaceutically acceptable salt thereof, of the first aspect of the invention and one or more therapeutically acceptable carriers.
  • pharmaceutically acceptable excipient or “pharmaceutically acceptable carrier”, “pharmaceutically acceptable diluent”, or “pharmaceutically acceptable vehicle”, as used interchangeably herein, refers to compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of a subject (e.g. human) without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio. Each carrier, excipient, etc., must also be “acceptable” in the sense of being compatible with the other ingredients of the formulation. Suitable carriers, excipients, etc. can be found in standard pharmaceutical texts, and include, as a way of example preservatives, agglutinants, humectants, emollients, and antioxidants.
  • the election of the pharmaceutical formulation will depend upon the nature of the active compound and its route of administration. Any route of administration may be used. In some embodiments, the route of administration is parenteral, and the composition is then appropriate for parenteral administration. In a particular embodiment, the route of administration is by injection. In a more particular embodiment, the route of administration is systemic, for example, by intramuscular, intravenous, intraarterial, intraperitoneal, subcutaneous, or transdermal injection. Topical administration is also contemplated, such that the pharmaceutical composition may be a topical composition.
  • compositions may be in any form, including, among others, tablets, pellets, capsules, aqueous or oily solutions, suspensions, emulsions, aerosols, or dry powdered forms suitable for reconstitution with water or other suitable liquid medium before use, for immediate or retarded release.
  • terapéuticaally effective amount means an amount of an active agent high enough to deliver the desired benefit (either the treatment or prevention of the illness), but low enough to avoid serious side effects within the scope of medical judgment.
  • the invention relates to the peptide, or a pharmaceutically acceptable salt thereof, according to the first aspect of the invention, or the pharmaceutical composition according to the second aspect of the invention, for use in therapy.
  • This aspect of the invention can also be formulated as the use of the peptide, or a pharmaceutically acceptable salt thereof, of the first aspect of the invention, or the pharmaceutical composition according to the second aspect of the invention, for the preparation of a medicament.
  • the present invention also relates to a method of treatment and/or prevention of a condition or disease comprising administering a therapeutically effective amount of the peptide of the invention, particularly together with pharmaceutically acceptable excipients and/or carriers, or the pharmaceutical composition of the invention to a subject in need thereof.
  • the subject is a mammal, more particularly a human.
  • the invention relates to the peptide, or a pharmaceutically acceptable salt thereof, of the first aspect of the invention, or the pharmaceutical composition according to the second aspect of the invention, for use in the treatment and/or prevention of a condition or disease caused or associated to the accumulation of fat in an organ or tissue, particularly in an organ, inflammation and/or fibrosis, in particular in a mammal, more particularly in a human.
  • This aspect of the invention can also be formulated as the use of the peptide, or a pharmaceutically acceptable salt thereof, of the first aspect of the invention, or the pharmaceutical composition according to the second aspect of the invention, for the preparation of a medicament for the treatment and/or prevention of a condition or disease caused or associated to the accumulation of fat in an organ or tissue, inflammation and/or fibrosis.
  • the present invention also relates to a method of treatment and/or prevention of a condition or disease caused or associated to the accumulation of fat in an organ or tissue, inflammation and/or fibrosis comprising administering a therapeutically effective amount of the peptide of the invention, particularly together with pharmaceutically acceptable excipients and/or carriers, or the pharmaceutical composition of the invention to a subject in need thereof.
  • the subject is a mammal, more particularly a human,
  • disease or condition caused or associated to the accumulation of fat in an organ refers to any disease characterized in that lipids are accumulated in an organ, in particular, associated to the accumulation of visceral fat.
  • disease or condition caused or associated to the accumulation of fat in a tissue refers to any disease characterized in that lipids are accumulated in a tissue, particularly selected from the list consisting of connective tissue, epithelial tissue, muscle tissue.
  • the disease or condition caused or associated to the accumulation of fat in an organ is characterized in an increased in the amount of visceral adipose tissue (VAT) in a subject.
  • VAT visceral adipose tissue
  • the disease or condition caused or associated to the accumulation of fat in an organ is selected from the list consisting of NAFLD, obesity, overweight, diabetes, lipohyperdystrophyand cardiovascular disease.
  • NAFLD non-alcoholic fatty liver disease
  • Healthy liver cells should contain little or no fat.
  • An essential criterion for the histological definition of NAFLD is the presence of lipid droplets in > 5% of hepatocytes. NAFLD is also defined when more than 5% of liver weight or volume corresponds to intrahepatic fat.
  • NAFLD fatty liver
  • steatosis fatty liver
  • NASH non-alcoholic steatohepatitis
  • ill hepatic fibrosis
  • cirrhosis cirrhosis
  • steatosis or "fatty liver”, as used herein is a condition characterized in that the liver cells start to build-up fat, although there is no inflammation or scarring at this stage. There are often no symptoms in this early stage. Approximately 20% of subjects with fatty liver, will develop non-alcoholic steatohepatitis or NASH.
  • non-alcoholic steatohepatitis is a condition corresponding to the stage of NAFLD in which the build-up of fat in the liver cells is accompanied with inflammation. Inflammation occurs when the liver is repairing damaged tissue. If the amount of damaged tissue increases, the liver may eventually not be able to repair it efficiently and the inflamed tissue will be modified into a scar, giving rise to hepatic fibrosis.
  • hepatic fibrosis is a condition characterized persistent inflammation that leads to scar tissue formation around the liver and nearby blood vessels. In this stage the liver is still able to function appropriately. Removing or treating the cause of the inflammation may prevent further progression or even reverse some of the damage. However, if over time, the scar tissue starts to replace a significant part of the normal liver tissue, the liver function ends up being affected, which ultimately leads to cirrhosis.
  • liver is the most severe stage of NAFLD, occurring after years of inflammation, where the liver becomes scarred and and permanently damaged; this permanent damage and can lead to liver failure (where the liver stops working properly) and liver cancer.
  • the disease or condition caused or associated to the accumulation of fat in an organ is NAFLD, in particular steatosis, NASH, hepatic fibrosis or cirrhosis, more particularly NASH.
  • the disease or condition caused or associated to the accumulation of fat in an organ is NASH.
  • the term "obesity”, as used herein refers to an abnormal or excessive fat accumulation in a subject, in particular a mammal, more in particular a human, that presents a risk to health.
  • the BMI associated to obesity in humans is of 30 or more. Obesity is frequently subdivided into 3 categories:
  • Class 1 obesity BMI of 30 to ⁇ 35
  • Class 2 obesity BMI of 35 to ⁇ 40
  • Class 3 obesity BMI of 40 or higher. Class 3 obesity is sometimes categorized as "severe” obesity.
  • body Mass Index refers to a subject's weight in kilograms (or pounds) divided by the square of height in meters (or feet).
  • the disease or condition caused or associated to the accumulation of fat in an organ is obesity, in particular class 1 obesity, class 2 obesity or class 3 obesity.
  • the disease is class 1 obesity.
  • the disease is class 2 obesity.
  • the disease is class 3 obesity.
  • the disease is class 1 or class 2 obesity.
  • the disease is class 2 or class 3 obesity.
  • weight refers to an abnormal or excessive fat accumulation in a subject, in particular a mammal, more in particular a human, that presents a risk to health, that is associated in humans to a BMI as defined above of between 25 and 30.
  • the disease or condition caused or associated to the accumulation of fat in an organ is overweight.
  • the disease or condition caused or associated to the accumulation of fat in an organ is NAFLD, obesity or overweight, preferably NASH, cirrhosis, obesity or overweight.
  • the disease or condition caused or associated to the accumulation of fat in an organ is NAFLD or obesity, particularly NASH, cirrhosis, or obesity.
  • diabetes refers to is a chronic disease that occurs either when the pancreas does not produce enough insulin or when the body cannot effectively use the insulin it produces. Insulin is a hormone that regulates blood glucose. Hyperglycaemia, also called raised blood glucose or raised blood sugar, is a common effect of uncontrolled diabetes and over time leads to serious damage to many of the body's systems, especially the nerves and blood vessels. The most common form of diabetes is diabetes type 2.
  • type 2 diabetes refers to a diabetes type characterized by insulin resistance, which may be combined with relatively reduced insulin secretion by the pancreas.ln a particular embodiment of the fourth aspect, the disease or condition caused or associated to the accumulation of fat in an organ is diabetes. In a more particular embodiment, it is diabetes type 2.
  • cardiovascular disease refers to conditions affecting the heart or blood vessels. It's usually associated with a build-up of fatty deposits inside the arteries (atherosclerosis) and an increased risk of blood clots.
  • lipohyperdistrophy refers to localized abnormal fat accumulation, most commonly of the intra-abdominal compartment (visceral adipose tissue [VAT]), breasts, dorso-cervical area (buffalo hump), and/or as discrete accumulations under the skin (lipomas).
  • disease caused or associated to inflammation refers to a disease characterized in that inflammation occurs in a part of the body, wherein inflammation is as defined above in the first aspect of the invention, and does not disappear, or the body does not return to a healthy non-inflamed state.
  • Non- limitative examples of inflammatory diseases include type 2 diabetes and rheumatoid arthritis.
  • RA rheumatoid arthritis
  • the disease may also affect other parts of the body, including skin, eyes, lungs, heart, nerves and blood. This may result in a low red blood cell count, inflammation around the lungs, and inflammation around the heart.[1] Fever and low energy may also be present. Often, symptoms come on gradually over weeks to months.
  • a disease associated or caused by fibrosis refers to a disease characterized in the appearance of fibrotic tissue, as indicated in the definition of "fibrosis” in the first aspect of the invention.
  • fibrotic diseases include hepatic fibrosis, adipose tissue fibrosis, pulmonary fibrosis, liver cirrhosis, systemic sclerosis, kidney fibrosis, progressive kidney disease, and cardiovascular fibrosis.
  • the disease associated to or caused by fibrosis is hepatic fibrosis, adipose tissue fibrosis, pulmonary fibrosis, liver cirrhosis, systemic sclerosis, progressive kidney disease, kidney fibrosis, and cardiovascular fibrosis.
  • the disease associated to or caused by fibrosis is hepatic fibrosis, adipose tissue fibrosis, pulmonary fibrosis kidney fibrosis, or cardiovascular fibrosis.
  • the disease associated to or caused by fibrosis is hepatic fibrosis or adipose tissue fibrosis, yet more particularly, hepatic fibrosis.
  • fibrotic diseases can be associated with aging.
  • scars resolve over time and are replaced by new tissue.
  • the scars do not always heal properly, and scar tissue can build up.
  • the disease associated to or caused by fibrosis is associated to aging.
  • the term "is associated to aging”, as used herein, refers to the fact that it is the consequence of or results from the process of aging in a subject.
  • the disease associated to or caused by fibrosis results from the process of aging.
  • the disease associated to or caused by fibrosis is hepatic fibrosis, adipose tissue fibrosis, pulmonary fibrosis, kidney fibrosis, or cardiovascular fibrosis, even more particularly hepatic fibrosis, and results from the process of aging.
  • the definitions and embodiments of the first and second aspects of the invention are equally applicable to the third and fourth aspects of the invention.
  • the invention relates to a cosmetic composition
  • a cosmetic composition comprising the peptide, or pharmaceutically acceptable salt thereof, of the first aspect of the invention, and one or more cosmetically acceptable carriers.
  • cosmetic composition in accordance with the present invention relates to a formulation that can be used for cosmetic purposes.
  • cosmetic purposes or uses refer to any purpose or uses for improving the bodily appearance of an animal body, preferably of a mammal, more preferably a human. Said purposes and uses are thus non-therapeutic.
  • cosmetically acceptable refers to excipients or carriers that are appropriate for use in contact with human skin without inappropriate allergic response, instability, incompatibility, or toxicity among others.
  • the cosmetic composition is a topical composition or an oral composition, particularly a topical composition.
  • the form of the cosmetic composition is any of those indicated for the pharmaceutical composition in the second aspect of the invention.
  • the invention relates to the use of the peptide, or a pharmaceutically acceptable salt thereof, of the first aspect of the invention, or of the cosmetic composition according to the fifth aspect of the invention, in cosmetics.
  • the cosmetic use, or the use in cosmetics, of the peptides and cosmetic composition according to the invention is to be applied to mammals, in particular humans, which are healthy subjects that need not have any diseases. That is, they can be subjects without a disease or condition associated with the accumulation of fat as defined above.
  • the cosmetic use is only for esthetical purposes aiming to improve the bodily appearance, and not to treat any disease.
  • the cosmetically effective amounts are different than therapeutically effective amounts, since in a cosmetic use the peptide has only to reach the fat accumulated or stored at subcutaneous level.
  • the cosmetic use of the invention is non-therapeutic. In another embodiment, the cosmetic use of the invention is non-surgical. In another embodiment of the invention, the cosmetic use of the invention is non-therapeutic and non-surgical.
  • the cosmetic effect of the peptides and cosmetic compositions of the invention derive from the lipolytic and/or anti-lipogenic effect provided by them. Therefore, the topical or dermal or oral, particularly dermal, administration of the peptides of the invention leads to the reduction of the subcutaneous fat herniated or accumulated within the fibrous connective tissue, such as cellulite.
  • Subcutaneous fat is found just beneath the skin, as opposed to visceral fat, which is found in the peritoneal cavity.
  • Subcutaneous fat can be measured using body fat calipers giving a rough estimate of total body adiposity. This fat aids in the process of homeostasis, by forming a layer of insulation to slow heat loss.
  • the cosmetic use of the invention is for reducing the subcutaneous fat in a mammal, preferably accumulated within the fibrous connective tissue under the skin of the mammal.
  • the cosmetic use of the invention is for reducing at least 5%, 10%, 20%, 30%, 40%. 50%, 60%, 70%, 80%, 90%, preferably at least 10% of the volume of the subcutaneous fat in a mammal, preferably accumulated within the fibrous connective tissue under the skin of the mammal.
  • Methods to determine the volume of fat in a particular region of a body are well known by an expert in the field.
  • Non- limitative examples of such methods include Magnetic resonance imaging (MRI), which allows to estimate the changes in adipose tissue volume before and after a treatment (such as the cosmetic non-therapeutic treatment of the invention).
  • MRI Magnetic resonance imaging
  • Subcutaneous fat can also be measured using body fat calipers. .
  • cellulite refers to persistent subcutaneous fat causing dimpling of the skin or nodularity, often on the pelvic region (specifically the buttocks), lower limbs, and abdomen in females.
  • the cosmetic use of the invention is for reducing cellulite in a mammal, preferably at least 5%, 10%, 20%, 30%, 40%. 50%, 60%, 70%, 80%, 90%, preferably at least 10% of the volume of the cellulite on a mammal.
  • the cellulite reduced is that located in any part of the body, such as the pelvic region (specifically the buttocks), lower limbs, or abdomen.
  • Methods to determine the amount of cellulite in a region of the body are commonly known to an expert in the field and also include Magnetic resonance imaging (MRI) to determine the adipose tissue volume in a part of the body, allowing to estimate the changes in cellulite volume before and after a treatment (such as the cosmetic non-therapeutic treatment of the invention), or the use of body fat calipers.
  • MRI Magnetic resonance imaging
  • the invention relates to a non-therapeutic method for reducing body weight in a subject with overweight, that comprises administering the peptide of the first aspect of the invention or the cosmetic composition of the fifth aspect of the invention, to said subject, wherein the subject is in particular a mammal, even more in particular a human.
  • the human is an adult human.
  • the human is a non-adult human.
  • the forms of the administered composition are as those disclosed in the second aspect of the invention for the pharmaceutical composition of the invention.
  • the route of administration is oral or dermal.
  • reducing overweight in a subject with overweight involves reducing the BMI of the subject at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, particularly at least 5%.
  • reducing overweight in a subject with overweight involves reducing the BMI of the subject at least 1 , at least 2, at least 3, at least 4, at least 5, at least 6, at least 7 points, particularly at least 1 point.
  • the definitions and embodiments of the first, second, third and fourth aspects of the invention are equally applicable to the fifth aspect of the invention.
  • the invention relates to a kit of parts comprising: a peptide, or pharmaceutically acceptable salt thereof, according to the first aspect of the invention, the pharmaceutical composition according to the second aspect of the invention, or the cosmetic composition according to the fifth aspect of the invention, and a device selected from the group consisting of an injection device, an implant, or a biodegradable container.
  • kits refers to a product comprising the products and/or compositions of the invention, packed so as to allow their transport and storage.
  • the kits of the invention can contain instructions far the simultaneous, sequential or separate use of the different components which are in the kit.
  • Said instructions can be in the form of printed material or in the form of an electronic support capable of storing instructions susceptible of being read or understood, such as, far example, electronic storage media (e.g. magnetic disks, tapes), or optical media (e.g. CD-ROM, DVD), or audio materials. Additionally or alternatively, the media can contain internet addresses that provide said instructions.
  • the invention relates to a device, such as an injection device, a patch, or a biodegradable container, comprising the peptide or pharmaceutically acceptable salt thereof according to he first aspect, the pharmaceutical composition according to the second aspect of the invention, or the cosmetic composition according to the fifth aspect of the invention.
  • injection device refers to a medical device designed to deliver a dose of a particular drug.
  • the injectors were initially designed to overcome the hesitation associated with selfadministration of a needle-based drug delivery device.
  • the injection device is syringe, or one or more micro-needles.
  • implant refers to devices or tissues that are placed inside or on the surface of the body. As used herein, said devices allow delivering medication in the body region where they are placed.
  • the implant is in the form of a patch.
  • biodegradable container refers to a device comprising degradable molecules in a more or less long time, often a few weeks to several months or even years after introduction into the skin.
  • first, second, third, fourth, fifth and sixth aspects of the invention are equally applicable to the seventh and eighth aspects of the invention.
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A
  • X 3 represents D or N
  • X 4 represents P, N, a basic amino acid or a hydrophobic amino acid, preferably P, N, L, V, or A,
  • X 5 represents E or Q
  • X 6 and X 7 are the same or different and represent A, V, L or I, X 8 represents F or P, subindexes "a”, “b”, “c”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1 and at least two of them represent 1 , wherein the peptide further comprises:
  • GDTNPKDDWF SEQ ID NO. 4
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A
  • X 4 represents P, N or L
  • X 6 and X 7 are the same or different and represent A, V, L or I;
  • X 8 represents F or P
  • subindexes "a”, “b”, “d”, “e”, “f” and “g”” are integer numbers independently selected from 0 and 1.-
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A
  • X 6 and X 7 are the same or different and represent A, V, L or I,
  • X 8 represents F or P
  • Subindexes "a”, “b”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1.
  • X 1 represents T, or A
  • X 2 represents W, N, Q, K or A
  • X 6 and X 7 are the same or different and represent A, V, L or I;
  • X 8 represents F or P, subindexes "a”, “b”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1.
  • - The peptide or pharmaceutically acceptable salt thereof according to any on of embodiments 1-2 wherein the peptide fragment F1 has a sequence SEQ ID NO. 8: (X 1 ) a (X 2 )bDNE G(X 6 )d(X 7 ) e (X 8 )f(Y) g , wherein:
  • X 1 represents T, or A
  • X 2 represents W, N, Q K or A
  • X 6 and X 7 are the same or different and represent A, V, L or I;
  • X 8 represents F or P, subindexes "a”, “b”, “d”, “e”, “f” and “g” are integer numbers independently selected from 0 and 1.
  • - The peptide, or pharmaceutically acceptable salt thereof according to any one of embodiments 1- 3, wherein the peptide fragment F1 has sequence SEQ ID NO. 9: TWDPEGVIFY.
  • - The peptide, or pharmaceutically acceptable salt thereof according to embodiment 1 , wherein the peptide fragment F1 has a sequence selected from the group consisting of SEQ ID NO.
  • peptide fragment F1 has a length of 5 to 9 amino acids, each one of the amino acids being a L- or D-amino acid, and sequence SEQ ID NQ.10: (T) a (X 2 ) b D(X 4 ) c EG(X 6 ) d (X 7 ) e (X 8 )f(Y) g wherein:
  • X 2 represents W, N, Q or K
  • X 4 represents P, N, a basic amino acid or a hydrophobic amino acid, preferably P, N, L, V, or A,
  • X 6 and X 7 are the same or different and represent A, V, L or I,
  • X 8 represents F or P
  • subindexes "a”, “b”, “c”, “d” “e”, “f” and “g” are integer numbers independently selected from 0 and 1 ; provided that two, three, four, five or six of the subindexes "a”, “b”, “c” “d”, “e”, “f' and “g” represent 1 ; and the remaining subindexes represent zero.
  • - X 6 and X 7 are the same or different and represent L, V, or A, and/or
  • peptide fragment F1 has a sequence from 5 to 9 amino acids, each one of the amino acids being L- or D-amino acid, and sequence SEQ ID NO.11 (T)a(X 2 ) b D(X 4 )EG(X 6 ) d (X 7 ) e (F) f (Y) g wherein:
  • X 2 represents W, N, Q or K
  • X 4 represents P, N or a basic amino acid
  • X 6 and X 7 are the same or different and represent A, V, L or I, subindexes "a”, “b”, “d” “e”, “f, and “g” are integer numbers independently selected from 0 and 1 ; provided that one, two, three, four or five of the subindexes "a”, “b”, “d” “e”, “f, and “g”represent 1; and the remaining subindexes represent zero.
  • X 2 represents W or N
  • X 4 represents P or N, and/or
  • X 6 or X 7 represents V, L or I .
  • peptide fragment F2 comprises SEQ ID NO. 13 (TKTSSSFEVR).
  • peptide fragment F2 comprises SEQ ID NO. 14 (VMTFDLTKITKTSSSFEVR).
  • peptide fragment F3 comprises SEQ ID NO. 15 (GDTNPKDDWFMLGLRDGRPE).
  • peptide fragment F1 is SEQ ID NO. 9 (TWDPEGVIFY)
  • peptide fragment F2 is SEQ ID NO. 13 (TKTSSSFEVR)
  • peptide fragment F3 is SEQ ID NO. 4 (GDTNPKDDWF).
  • TKTSSSFEVRTWDPEGVIFY The peptide, or pharmaceutically acceptable salt thereof according to any one of the previous embodiments that has sequence SEQ ID NO. 16 (TKTSSSFEVRTWDPEGVIFY), SEQ ID NO. 17 (TWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 18 (TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF), SEQ ID NO. 19 (TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE), or SEQ ID NO. 20 (VMTFDLTKITKTSSSFEVRTWDPEGVIFY).
  • SEQ ID NO. 16 TKTSSSFEVRTWDPEGVIFY
  • SEQ ID NO. 17 TWDPEGVIFYGDTNPKDDWF
  • SEQ ID NO. 18 TKTSSSFEVRTWDPEGVIFYGDTNPKDDWF
  • SEQ ID NO. 19 TWDPEGVIFYGDTNPKDDWFMLGLRDGRPE
  • SEQ ID NO. 20 VMTFDLTKITKT
  • the N-terminal end of the peptide corresponds to -NR1R2, being R1 and R2 independently selected from the group consisting of -H, -C(O)R3, a triglyceride, (Ci-C2o)alkyl and (Ci-C2o)alkenyl and R3 is -H, (Ci-C2o)alkyl or (Ci-C2o)alkenyl; and
  • R4 to Re are radicals independently selected from the group consisting of: -H and (Ci-C2o)alkyl.
  • a pharmaceutical composition comprising a therapeutical effective amount of a peptide, or pharmaceutically acceptable salt thereof, as defined in any one of the previous embodiments and one or more therapeutically acceptable carriers.
  • NASH non-alcoholic steatohepatitis
  • hepatic fibrosis hepatic fibrosis
  • cirrhosis hepatic steatosis
  • overweight obesity
  • obesity inflammatory disease
  • lipohyperdystrophy diabetes and cardiovascular disease.
  • NASH non-alcoholic steatohepatitis
  • 56- A cosmetic composition comprising the peptide, or pharmaceutically acceptable salt thereof, according to any one of embodiments 1-50 and one or more cosmetically acceptable carriers.
  • kits of parts comprising: a peptide or pharmaceutically acceptable salt thereof as defined in any one of embodiments 1-50, the pharmaceutical composition according to embodiment 51, or the cosmetic composition according to embodiment 56, and a device selected from the group consisting of an injection device, an implant, or a biodegradable container.
  • 61- A device such as an injection device, an implant, or a biodegradable container, comprising the peptide or pharmaceutically acceptable salt thereof as defined in any one of embodiments 1-50, the pharmaceutical composition as defined in embodiment 51 or the cosmetic composition as defined in embodiment 56.
  • the method for peptide production is solid phase peptide synthesis (SPPS).
  • SPPS solid phase peptide synthesis
  • the Fmoc chemistry is always used. SPPS is to sequentially add amino acids to the resin to build a peptide chain.
  • the Fmoc group at N-terminal is first de-protected, and then, the side chain protection group deprotected, and the peptide is cleaved off from the Resin.
  • the specific procedure is as follows (see Fig. 1):
  • Detection reagent and a spot of resin were taken into one test tube. And then the test tube was put into high temperature water for seconds to check if the color of the resin was changed. If the color of the resin changed, the Fmoc groups were removed successfully. 5. Coupling
  • the peptide is cleaved off from the Resin.
  • the characterization data of the peptides are provided in table 5 bellow.
  • the synthesized peptides are provided in table 5 bellow.
  • Example 2 Effects of peptides GP4, GP7, GP8 and GP9 (peptides with SEQ ID NO. 20, SEQ ID NO. 17, SEQ ID NO. 18, SEQ ID NO. 19, respectively) in hepatic lipogenesis in HepG2 cells, fibrosis in LX-2 cells and in lipolysis in human mature adipocytes
  • HepG2 hepatoblastoma cells (cat. no. HB-8065; ATCC, LGC Standards SLU, Barcelona, Spain) were maintained in Dulbecco's modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum and antibiotics. HepG2 cells were treated with vehicle or 10 piM of GP4, GP7, GP8 and GP9 for 24h. LX-2 human hepatic stellate cells (SCC064) were maintained in DMEM supplemented with 2% fetal bovine serum and antibiotics.
  • DMEM Dulbecco's modified Eagle medium
  • LX-2 were cultured for 24h in DMEM 0.2% FBS and treated for 24h with vehicle or TGFpl (20ng/ml) in the absence or presence of 8 piM of GP4, GP7, GP8 and GP9 for 24h.
  • cells were harvested for gene expression analysis.
  • Human preadipocytes and cell culture reagents were from purchased from Tebu-Bio (Tebu-bio, Barcelona, Spain) and differentiation protocol was done following the manufacturer's instructions. Human adipocytes were maintained in a humidified incubator with 5% CO2 at 37°C (Sex hormone-binding globulin overexpression protects against high-fat diet-induced obesity in transgenic male mice. Saez-Lopez C, Villena JA, Simb R, Selva DM. J Nutr Biochem. 2020 Nov;85: 108480. doi: 10.1016/j.jnutbio.2020.108480).
  • Lipolysis assays were performed using a Lipolysis Kit (Tebu-Bio) following the manufacturer's instructions as previously described.
  • SYBRGreen Invitrogen SA
  • GP4, GP5, GP8 and GP9 showed different activities in regulating key hepatic lipogenic enzymes such as Acetyl-CoA Carboxylase (ACC), Fatty Acid Synthase (FAS) and ATP-Citrate Lyase (ACLY) in HepG2 cells ( Figure 5).
  • ACC Acetyl-CoA Carboxylase
  • Fatty Acid Synthase Fatty Acid Synthase
  • ACLY ATP-Citrate Lyase
  • GP8 and GP9 showed different activities in regulating collagen 1A1 expression induced by TGFpl in human hepatic stellate cell line (LX-2). Col1A1 mRNA levels were reduced by treatment with GP8 (31 %) and GP9 (21 %) ( Figure 6).
  • GP4, GP8 and GP9 treatment induced lipolysis measured by glycerol production after 16h treatment in human mature adipocytes (Figure 7).
  • the lipolysis positive control (isoproterenol) increased glycerol concentration in a 370% with respect with the control while GP4 was able to increase glycerol production by 500%, GP8 by 370% and GP9 by 170% (Fig. 7)
  • Peptide GP6 (peptide with SEWQ ID NO. 16) reduces hepatic lipogenesis in HepG2 cells, fibrosis in LX-2 cells and induces lipolysis in human mature adipocytes
  • HepG2 hepatoblastoma cells (cat. no. HB-8065; ATCC, LGC Standards SLU, Barcelona, Spain) were maintained in Dulbecco's modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum and antibiotics. HepG2 cells were cultured for 5 day in the absence or presence of 30mM fructose. Cells cultured in 30mM fructose were daily treated with vehicle, Telmisartan, Semaglutide or GP6. LX-2 human hepatic stellate cells (SCC064) were maintained in DMEM supplemented with 2% fetal bovine serum and antibiotics.
  • DMEM Dulbecco's modified Eagle medium
  • LX-2 were cultured for 24h in DMEM 0.2% FBS and treated for 24h with vehicle or TGFpl (20ng/ml) in the absence or presence of GP6 (10 or 40pig/ml). At the end of the experiment's cells were harvested for gene expression analysis.
  • Lipolysis assays were performed using a Lipolysis Kit (Tebu-Bio) following the manufacturer's instructions as previously described by Saez-Lopez and collaborators (Sex hormone-binding globulin overexpression protects against high-fat diet-induced obesity in transgenic male mice. Saez-Lopez C, Villena JA, Simo R, Selva DM. J Nutr Biochem. 2020 Nov;85: 108480. doi: 10.1016/j.jnutbio.2020.108480.)
  • SYBRGreen Invitrogen SA
  • GP6 reduces hepatic lipogenesis in HepG2 cells
  • GP6 Daily treatment with GP6 reduced significantly hepatic lipogenesis induced by 30mM fructose via reducing mRNA levels of a key hepatic lipogenic enzyme such as Acetyl-CoA Carboxylase (ACC) and a key transcription factor regulating several lipogenic enzymes such as PPARy in HepG2 cells ( Figure 2).
  • ACC Acetyl-CoA Carboxylase
  • PPARy a key transcription factor regulating several lipogenic enzymes
  • GP6 treatment was significantly much more effective than Telmisartan and Semaglutide, used as positive controls, in reducing the induced expression of ACC and PPARy by 30mM fructose treatment (Fig. 2).
  • GP6 induces lipolysis in human mature adipocytes
  • GP6 induced lipolysis measured by glycerol production after 16h treatment in human mature adipocytes ( Figure 4).
  • the lipolysis positive control (isoproterenol) increased glycerol concentration in a 400% with respect with the controls while GP6 was able to increase glycerol production in a dose dependent manner by 200% (25pig/ml), 270% (50pig/ml) and 315% (100pig/ml) performing more efficiently than Semaglutide (165% increase) (Fig. 4).
  • - GP6 has anti-lipogenic activity by inhibiting the expression of ACC and PPARy, two key players of hepatic lipogenesis in human liver cells (HepG2 cells).
  • - GP6 has anti-fibrotic activity by inhibiting the expression of collagen 1A1 in human hepatic stellate cells (LX-2 cells).
  • - GP6 has lipolytic activity by increasing lipolysis in human mature adipocytes.
  • Example 4 Preventive effects of peptide GP6 (SEQ ID NO. 16) in an obesity and faty liver disease mouse model
  • mice C57BL6/J male mice were purchased and kept for quarantine and acclimatization for a period of about 7 days before initiation of every experiment. Mice were housed in clean and sterilized mice cages and maintained in a controlled environment with 22+3° C temperature, 50+20% humidity, a light/dark cycle of 12 hours each and 15-20 fresh air changes per hour.
  • mice were fed ad libitum, either with chow diet (150SP-10, Safe Diets) or 45% high-fat diet (TD.190179, Envigo) plus 30% fructose (F0127, Sigma Aldrich) in drinking water for 8 weeks in the daily presence of vehicle or a subcutaneous injection of GP6 (20mg/kg/day).
  • chow diet 150SP-10, Safe Diets
  • TD.190179, Envigo 30% fructose
  • F0127 Sigma Aldrich
  • mice were sacrificed, serum samples were extracted, tissues were weighted and part was fixed in paraformaldehyde for histology studies and part immediately frozen at -80C for mRNA and protein expression studies as well as assessment of triglycerides.
  • livers and adipose tissue were fixed in 4% paraformaldehyde for 24 hours and embedded in paraffin.
  • Serial 5-mm-thick sections were used for histological examination and stained with hematoxylin eosin (H&E) and Picrosirius red for histological examination following standard procedures. Briefly, sections were alcohol-xylol hydrated at room temperature, and subsequently, they were stained at room temperature in a solution of 0.1 % Direct Red 80 (Sigma-Aldrich) in a saturated aqueous solution of picric acid (Sigma-Aldrich) for 1 h.
  • H&E hematoxylin eosin
  • Picrosirius red for histological examination following standard procedures. Briefly, sections were alcohol-xylol hydrated at room temperature, and subsequently, they were stained at room temperature in a solution of 0.1 % Direct Red 80 (Sigma-Aldrich) in a saturated aqueous solution of picric acid (Sigma
  • liver steatosis and/or fibrosis were assessed blinded by an experienced pathologist according to the NASH-clinical research network scoring system (Design and validation of a histological scoring system for nonalcoholic fatty liver disease.
  • Serum levels of AST and ALT were measured using MAK055 and MAK052 from Sigma-Aldrich respectively following the manufacture's instructions.
  • Hepatic TG content was measured from liver extracts using a Triglyceride Assay Kit (ab65336) following the manufacture's instructions.
  • SYBRGreen Invitrogen SA
  • GP6 treatment reduces total liver and adipose tissue weight
  • Fibrosis graded 0 (absent) to 4 (1 , perisinusoidal/pericellular fibrosis; 2, periportal fibrosis; 3, bridging fibrosis; 4, cirrhosis)] as well as the percentage of steatosis (Fig. 11).
  • PPARY mRNA levels in hepatic tissue which is the major transcription factor regulating the expression of key hepatic lipogenic enzymes (ACC and FAS).
  • ACC and FAS key hepatic lipogenic enzymes
  • GP6 Daily subcutaneous injection with GP6 (20mg/kg/day) reduced hepatic inflammation when compared with vehicle treated mice. This was evident since GP6 treatment reduced expression of F480 mRNA levels in the corresponding hepatic tissue a marker for macrophage infiltration. In addition, GP6 treatment reduced the hepatic expression of proinflammatory cytokines such as TNFo, IL1
  • proinflammatory cytokines such as TNFo, IL1
  • GP6 treatment reduces adipose tissue inflammation
  • - GP6 protects against obesity development by reducing total body weight gain and subcutaneous and visceral adipose tissue weight induced by a high fat diet feeding and 30% fructose in the drinking water.
  • GP6 protects against fatty liver disease development by reducing hepatic total liver weight and lipid accumulation induced by a high fat diet feeding and 30% fructose in the drinking water.
  • GP6 reduced the hepatic lipogenesis by inhibiting the expression PPARY mRNA levels, which is the major transcription factor regulating hepatic lipogenesis and by reducing the expression of key hepatic lipogenic enzymes such as ACC and FAS.
  • - GP6 protects against hepatic and adipose tissue inflammation induced by a high fat diet feeding and 30% fructose in the drinking water by reducing the expression of F480 mRNA levels, a marker for macrophage infiltration in liver and adipose tissue as well as by reducing the hepatic expression of proinflammatory cytokines such as TNFo, IL113 and IL6.
  • - GP6 protects against adipose tissue fibrosis development induced by a high fat diet feeding and 30% fructose in the drinking water by reducing the expression of Colal al mRNA levels.
  • Example 5 Preventive effects of peptide GP6 (SEQ ID NO. 16) in a CCI4-induced fibrosis mouse model
  • mice C57BL6/J male mice were purchased and kept for quarantine and acclimatization for a period of about 7 days before initiation of every experiment. Mice were housed in clean and sterilized mice cages and maintained in a controlled environment with 22+3° C temperature, 50+20% humidity, a light/dark cycle of 12 hours each and 15-20 fresh air changes per hour.
  • mice were sacrificed, serum samples were extracted, tissues were weighted and part was fixed in paraformaldehyde for histology studies and part immediately frozen at -80C for mRNA and protein expression studies.
  • Serum analysis showed that daily subcutaneous treatment with GP6 (20mg/kg/day) reduced the ALT serum levels (approximately by 50%) but not the AST serum levels when compared with vehicle treated mice (Fig. 17).
  • GP6 protects against hepatic fibrosis development induced by CCI4 treatment by reducing hepatic collagen accumulation. Mechanistically, GP6 reduced the expression of hepatic Colal al mRNA levels.
  • - GP6 protects against hepatic inflammation induced by CCI4 treatment by reducing the expression of F480 mRNA levels, a marker for macrophage infiltration in liver.
  • Example 6 Therapeutic effects of peptide GP6 (SEQ ID NO. 16) in an obesity and fatty liver disease mouse model
  • mice C57BL6/J male mice were purchased and kept for quarantine and acclimatization for a period of about 7 days before initiation of every experiment. Mice were housed in clean and sterilized mice cages and maintained in a controlled environment with 22+3° C temperature, 50+20% humidity, a light/dark cycle of 12 hours each and 15-20 fresh air changes per hour.
  • vehicle water
  • Telmisartan 5mg/kg/day
  • GP6 20mg/kg/day
  • mice were sacrificed, serum samples were extracted, tissues were weighted and part was fixed in paraformaldehyde for histology studies and part immediately frozen at -80C for mRNA and protein expression studies as well as assessment of triglycerides.
  • GP6 treatment reduces total body weight and liver Total body weight was significantly increased by high fat diet and 30% fructose in the drinking water in the vehicle and Telmisartan (as positive control) treated group when compared with control mice, while GP6 treated mice were not significantly heavier than control mice at the end of the experiment.
  • Results also showed liver weight was increased by high fat diet and 30% fructose in the drinking water in the vehicle treated mice when compared with control mice. While Telmisartan did not reduced significantly the liver weight, GP6 treatment reduced significantly when compared with vehicle treated mice (Fig. 21).
  • Serum analysis showed that daily subcutaneous treatment with GP6 (20mg/kg/day) reduced the increase glucose levels induced by high fat diet and 30% fructose in the drinking water when compared with vehicle treated mice while Telmisartan did not have any effect when compared with vehicle treated mice.
  • AST serum levels were also reduced significantly by the GP6 treatment (Fig. 22).
  • GP6 The antilipogenic activity of GP6 was also corroborated and supported by measuring PPARY mRNA levels, which is the major transcription factor regulating the expression of a key hepatic lipogenic enzymes such as ACC. As it can be seen below, daily subcutaneous treatment with GP6 (20mg/kg/day) reduced the mRNA levels of PPARY and ACC in hepatic tissue when compared with vehicle treated mice (Fig. 25).
  • TGFpl is the main factor activating hepatic stellate cells which will produce collagen in fibrosis development.
  • GP6 protects against obesity development by reducing total body weight gain induced by a high fat diet feeding and 30% fructose in the drinking water.
  • - GP6 protects against hyperglycemia induced by a high fat diet feeding and 30% fructose in the drinking water.
  • - GP6 reduces fatty liver disease by reducing hepatic lipid accumulation induced by a high fat diet feeding and 30% fructose in the drinking water.
  • GP6 reduced the hepatic lipogenesis by inhibiting the expression PPARY mRNA levels, which is the major transcription factor regulating hepatic lipogenesis and by reducing the expression of key hepatic lipogenic enzyme such as ACC.
  • - GP6 protects against hepatic fibrosis development induced by a high fat diet feeding and 30% fructose in the drinking water by reducing the expression of Colal al and TGFp-1 mRNA levels.
  • - GP6 reduces hepatic and adipose tissue inflammation induced by a high fat diet feeding and 30% fructose in the drinking water by reducing the expression of F480 mRNA levels, a marker for macrophage infiltration in liver and adipose tissue as well as by reducing the hepatic expression of proinflammatory cytokines such as TNFo and IL1 p.
  • - GP6 protects against adipose tissue and heart fibrosis development induced by a high fat diet feeding and 30% fructose in the drinking water by reducing the expression of Colal al mRNA levels.
  • HepG2 hepatoblastoma cells (cat. no. HB-8065; ATCC, LGC Standards SLU, Barcelona, Spain) were maintained in Dulbecco's modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum and antibiotics.
  • DMEM Dulbecco's modified Eagle medium
  • HepG2 cells were cultured for 5 day in the absence or presence of 30mM fructose.
  • Cells cultured in 30mM fructose were daily treated with vehicle, Telmisartan, Semaglutide or EDL6D.
  • GP6 40pig/ml
  • GP10 40pig/ml
  • GP11 40
  • GP12 40pg/ml
  • GP13 40pg/ml
  • SHBG 20nM
  • LX-2 human hepatic stellate cells (SCC064) were maintained in DMEM supplemented with 2% fetal bovine serum and antibiotics.
  • LX-2 were cultured for 24h in DMEM 0.2% FBS and treated for 24h with vehicle or TGFpl (20ng/ml) in the absence or presence of EDL6D (10 or 40pig/ml). At the end of the experiment's cells were harvested for gene expression analysis.
  • Human preadipocytes and cell culture reagents were from purchased from Tebu-Bio (Tebu-bio, Barcelona, Spain) and differentiation protocol was done following the manufacturer's instructions. Human adipocytes were maintained in a humidified incubator with 5% CO2 at 37°C (Saez-Lopez et al Journal Nutritional Biochemistry 2020).
  • Lipolysis assays were performed using a Lipolysis Kit (Tebu-Bio) following the manufacturer's instructions (Saez-Lopez et al Journal Nutritional Biochemistry 2020).
  • livers and adipose tissue were fixed in 4% paraformaldehyde for 24 hours and embedded in paraffin.
  • Serial 5-mm-thick sections were used for histological examination and stained with hematoxylin eosin (H&E) and Picrosirius red for histological examination following standard procedures. Briefly, sections were alcohol-xylol hydrated at room temperature, and subsequently, they were stained at room temperature in a solution of 0.1% Direct Red 80 (Sigma-Aldrich) in a saturated aqueous solution of picric acid (Sigma-Aldrich) for 1 h.
  • Direct Red 80 Sigma-Aldrich
  • picric acid Sigma-Aldrich
  • Serum levels of AST and ALT were measured using MAK055 and MAK052 from Sigma-Aldrich respectively following the manufacture's instructions.
  • Hepatic TG content was measured from liver extracts using a Triglyceride Assay Kit (ab65336) following the manufacture's instructions.
  • HepG2 cells were cultured for 24h in the absence or presence of GP10, GP11 , GP12, GP13 or GP6.
  • Results showed that GP10, GP11 and GP6 reduced the mRNA levels of a key hepatic lipogenic enzyme such as Acetyl-CoA Carboxylase (ACC), ATP Citrate Lyase (ACLY) and Fatty Acid Synthase (FAS) and a key transcription factor regulating several lipogenic enzymes such as PPARy when compared with vehicle treated HepG2 cells ( Figure 32).
  • ACC Acetyl-CoA Carboxylase
  • ACLY ATP Citrate Lyase
  • PPARy a key transcription factor regulating several lipogenic enzymes
  • PPARy a key transcription factor regulating several lipogenic enzymes
  • GP6 treatment reduced the mRNA levels of collagen 1 A1 induced by TGFpl in human hepatic stellate cell line (LX-2). GP10, GP11 , GP12 and GP13 carrying 2 aa substitutions had similar results than GP6 treatment. All peptides were more effective than SHBG in reducing Col1A1 expression ( Figure 33).
  • HepG2 cells were cultured in the absence or presence of 30mM fructose for 2h and treated with vehicle or GP10, GP11, GP12, GP13, GP4, GP6, GP7, GP8, GP9 or SHBG. Results showed that treatment with GP10, GP11 , GP12, GP4, GP6, GP8 or SHBG was able to reduce the fructose-induced increase expression of key lipogenic enzymes (ACC, ACLY, FAS and PPARy). GP13 and GP9 treatments were able to reduce the expression of ACC and ACLY more effectively than SHBG but had no effect on FAS and increased PPARy expression. GP7 treatment was able to reduce the expression of ACC and ACLY more effectively than SHBG but had no effect on FAS and PPARy expression ( Figure 34). Citation List
  • Sex hormone-binding globulin overexpression protects against high-fat diet-induced obesity in transgenic male mice.
  • Transforming growth factor-beta 1 A new factor reducing hepatic SHBG production in liver fibrosis. Briansb-Llort L, Fuertes-Rioja L, Ramos-Perez L, Salcedo-Allende MT, Hernandez C, Simb R, Selva DM. J Cell Physiol. 2022 Sep;237(9):3598-3613. doi: 10.1002/jcp.30818.

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Abstract

L'invention concerne des peptides, ou des sels pharmaceutiquement acceptables de ceux-ci, les peptides ayant une longueur de 10 à 40 acides aminés, chacun des acides aminés étant un acide aminé L ou D et comprenant, un fragment peptidique F1 avec SEQ ID NO 9 : TWDPEGVIFY ou qui est un variant de séquence de celui-ci qui a au moins 80% d'identité de séquence avec SEQ ID NO. 9, chacun des acides aminés du fragment peptidique F1 étant un acide aminé L ou D ; et comprenant en outre : un fragment peptidique F2 à l'extrémité N-terminale du fragment peptidique F1, avec SEQ ID NO. 13 (TKTSSSFEVR) ou qui est un variant de séquence de celui-ci avec au moins 80% d'identité de séquence avec SEQ ID NO. 13 ; ou avec SEQ ID NO. 14 (VMTFDLTKITKTSSSFEVR) ou qui est un variant de séquence de celui-ci avec au moins 80% d'identité de séquence avec SEQ ID NO. 14 ; et chacun des acides aminés du fragment peptidique F2 étant un acide aminé L ou D ; et/ou un fragment peptidique F3 à l'extrémité C-terminale du fragment peptidique F1, avec SEQ ID NO. 4 (GDTNPKDDWF) ou qui est un variant de séquence de celui-ci avec au moins 80% d'identité de séquence avec SEQ ID NO. 4 ; ou avec SEQ ID NO. 15 (GDTNPKDDWFMLGLRDGRPE) ou qui est un variant de séquence de celui-ci avec au moins 80% d'identité de séquence avec SEQ ID NO. 15 ; et chacun des acides aminés du fragment peptidique F3 étant un acide aminé L ou D. Ces peptides présentent une activité lipolytique, anti-lipogène, antifibrotique et anti-inflammatoire. L'invention concerne également l'utilisation médicale desdits peptides pour le traitement de maladies provoquées ou associées à l'accumulation de graisse dans un organe ou un tissu, une inflammation et/ou une fibrose, telles que la NAFLD, en particulier la NASH, ou l'obésité.
PCT/EP2024/065136 2023-06-02 2024-06-01 Peptides à activité lipolytique, anti-lipogène, antifibrotique et anti-inflammatoire Pending WO2024246354A1 (fr)

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