US20070224285A1 - Agent for Preventing or Suppressing Hepatopathy and Functional Food for Preventing or Suppressing Hepatopathy - Google Patents
Agent for Preventing or Suppressing Hepatopathy and Functional Food for Preventing or Suppressing Hepatopathy Download PDFInfo
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- US20070224285A1 US20070224285A1 US10/599,447 US59944705A US2007224285A1 US 20070224285 A1 US20070224285 A1 US 20070224285A1 US 59944705 A US59944705 A US 59944705A US 2007224285 A1 US2007224285 A1 US 2007224285A1
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- hepatic dysfunction
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/20—Milk; Whey; Colostrum
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
- A61K35/741—Probiotics
- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
- A61K35/741—Probiotics
- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
- A61K35/747—Lactobacilli, e.g. L. acidophilus or L. brevis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
Definitions
- the present invention relates to an agent for preventing or suppressing hepatic dysfunction, and functional food, such as foods for specified health uses, for preventing or suppressing hepatic dysfunction.
- the present invention relates to an agent and functional food for preventing or suppressing hepatic dysfunction, which suppress the elevation of serum GOT and GPT levels caused by hepatocellular necrosis to prevent and/or suppress hepatic dysfunction.
- Liver is a central organ of metabolism, and has a variety of important functions, such as biligenesis, excretion, detoxication, and the like.
- liver is said to be a silent organ due to its great reserve, and hardly develops symptoms, such as malaise, jaundice, edema, and ascites, so that its dysfunction tends to be perceived too late.
- GOT glutamic-oxaloacetic transaminase
- GPT glutamic-pyruvic transaminase
- glycyrrhizin formulation such as Stronger Neo-Minophagen C (registered trade mark, manufactured by MINOPHAGEN PHARMACEUTICAL, CO., LTD.) is sometimes used for chronic liver diseases, such glycyrrhizin formulation is inactivated in the intestines, so that desired effect cannot be expected through oral administration, and parenteral injection is the main route of administration.
- side effects such as hypertension or hypokalemia
- amino acid formulations are sometimes used for the purpose of ameliorating hepatic encephalopathy or hypoalbuminemia associated with liver diseases such as cirrhosis or hepatic insufficiency.
- such amino acid formulations are used with mere expectation of improvement in nutritional deficiency caused by liver diseases, i.e., improvement in nitrogen metabolism or reduction of blood ammonia level by balancing the plasma amino acid, rather than treatment of liver diseases.
- Lactoferrin is known to be contained in milks of various mammals.
- lactoferrin is prone to thermal denaturation, and known to be denatured easily in ordinary high temperature pasteurization or the like process (see, for example, Non-patent Publications 1 to 3).
- isolation or use of lactoferrin in industrial scale is restricted, and problems remain in cost and versatility.
- Whey has recently come to be known to contain various components having physiological functions, such as components for protecting gastric mucosa ( ⁇ -lactalbumin)
- ⁇ -lactalbumin components for protecting gastric mucosa
- an agent for preventing or suppressing hepatic dysfunction comprising whey as an active component.
- a method for preventing or suppressing hepatic dysfunction in need thereof an effective amount of an agent for preventing or suppressing hepatic dysfunction comprising whey as an active component is provided.
- whey for the manufacture of an agent for preventing or suppressing hepatic dysfunction.
- whey for the manufacture of functional food for preventing or suppressing hepatic dysfunction.
- the agent for preventing or suppressing hepatic dysfunction according to the present invention contains whey, which has been taken as food, as the active component, the agent may be taken daily and continuously, is excellently safe, and may effectively prevent and/or suppress hepatic dysfunction, such as hepatocellular necrosis. Since the functional food for preventing or suppressing hepatic dysfunction according to the present invention contains the present agent for preventing or suppressing hepatic dysfunction, the present functional food may be expected to prevent and/or suppress hepatic dysfunction.
- the agent for preventing or suppressing hepatic dysfunction according to the present invention contains whey as the active component, and is capable of effectively preventing and/or suppressing, for example, the elevation of blood GOT and GPT levels which is said to be ascribable mainly to hepatocellular necrosis.
- the active component, whey includes an aqueous fraction of milk obtained by removing all or most of the casein protein and the like from milk according to a common procedure, and may be, for example, acid whey and/or cheese whey.
- the acid whey may include fermented milk whey obtained by fermentation of milk with lactic acid bacteria, and casein whey containing an aqueous fraction of milk obtained by adding acid to milk to remove all or most of the casein protein and the like according to a common procedure.
- Fermented milk whey is particularly preferred for its excellent ability to prevent and/or suppress hepatic dysfunction.
- the fermented milk whey may usually be a fermented milk whey prepared by fermentation of milk with lactic acid bacteria, or by symbiotic fermentation of milk with lactic acid bacteria and a yeast.
- the starting material milk may be animal milk, such as cow's milk, goat's milk, or sheep's milk; vegetable milk, such as soy bean milk; or processed milk thereof, such as skim milk, reconstituted milk, powdered milk, or condensed milk.
- the milk may be in the form of a mixture.
- the solid content of the milk is not particularly limited
- the solid non-fat content is typically about 9 mass %.
- the solid non-fat content may be increased to some extent.
- the fermented milk whey obtained in the production of fermented milk may be separated from other milk components before use, but when the fermented milk whey is to be made into the functional food or the like to be discussed later, such other milk components are not necessarily separated.
- the lactic acid bacteria may be chose of the genus Streptococcus, Lactococcus, Lactobacillus, Bifidobacterium, or the like, with Lactobacillus being preferred.
- Lactobacillus may include Lactobacillus bulgaricus, Lactobacillus helveticus, Lactobacillus casei, Lactobacillus acidophilus, and Lactobacillus fermentum, with Lactobacillus heiveticus being particularly preferred.
- Lactobacllius helveticus ATCC 15009 Lactobacillus heiveticus ATCC 521
- Lactobacillus helveticus CM4 strain (deposited at National Institute of Advanced Industrial Science and Technology, International Patent Organism Depositary under Accession Number FERM BP-6060 on Aug. 15, 1997) (referred to as CM4 hereinbelow) may be used, with CM4 being particularly preferred.
- CM4 has been deposited under the above-mentioned accession number under the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure. All restrictions on the availability to the public of this strain will be irrevocably removed upon the granting of a patent.
- the lactic acid bacteria are preferably in the form of a pre-cultured starter having sufficiently high activity.
- the initial cell count may preferably be about 10 5 -10 7 cells/ml.
- yeast When the fermented milk whey is to be used in functional food, such as foods for specified health uses, yeast may be used for symbiotic fermentation for improved flavor and palatability.
- the strain of the yeast is not particularly limited, and may preferably be, for example, yeast of the genus Saccharomyces, such as Saccharomyces cerevisiae.
- the content of the yeast may suitably be selected depending on the purpose.
- the fermentation may be carried out by culturing one or more kinds of the lactic acid bacteria in a medium, or culturing a mixture of one or more kinds of the lactic acid bacteria and one or more kinds of the yeast in a medium.
- the medium may be those composed only of one or more kinds of the milk components mentioned above, or those optionally contain additional components, such as yeast extract; vitamins, e.g. ascorbic acid; amino acids, e.g. cysteine; salts, e.g. sodium chloride; sugars, e.g. glucose, sucrose, raffinose, or stachyose; stabilizers, e.g. gelatine; and flavoring agents.
- the fermentation may be performed usually by static or stirred culture, for example at 20 to 50° C., preferably 30 to 45° C., at the initial pH of 6.0 to 7.0, and may be terminated when the cell count becomes 10 7 cells/ml or higher at pH 5.0 or lower.
- the milk may be subjected to high-temperature pasteurization before fermentation.
- the fermented milk whey may be separated from curd by means of a common separating operation.
- the fermented milk whey as the active component is to be used in the functional food to be discussed later, the fermented milk containing the whey may be used as it is without separation, if so desired, or the extent of separation may suitably be decided.
- the casein whey may be prepared by, when solid milk, such as whole milk or skim milk is used, dissolving the milk in distilled water, adding, for example, lactic acid, citric acid, acetic acid, tartaric acid, fumaric acid, malic acid, aluconic acid, or adipic acid to adjust the acidity to a level suitable for removing protein, typically casein, and separating the whey component (aqueous fraction) by a common procedure, such as membrane filtration.
- the milk may be subjected to high temperature pasteurization before the acid is added.
- the acid may usually be added in an amount for achieving 1.0 to 4.0% acidity, depending on the kind of the acid or the like.
- the cheese whey may be prepared in the ordinary cheese production, by coagulating milk with rennet to form curd, and separating the whey component from the curd by centrifugation or the like.
- the milk may be subjected to high temperature pasteurization before the rennet is added.
- the dose of the whey as the active component in the present agent for preventing or suppressing hepatic dysfunction is not particularly limited, taking the continuity of administration into account, and may usually be not less than 0.001 g per kg body weight per day, preferably not less than 0.01 g per kg body weight per day, in terms of freeze-dried powder.
- the agent for preventing or suppressing hepatic dysfunction of the present invention may optionally contain components other than the whey as desired, having the function of preventing or suppressing hepatic dysfunction.
- the agent for preventing or suppressing hepatic dysfunction according to the present invention may be in a whey concentrate obtained by concentrating whey through vacuum concentration or the like process, or a dried whey powder obtained by drying whey through freeze-drying or spray drying.
- the agent for preventing or suppressing hepatic dysfunction according to the present invention may be administered usually through an oral route.
- the agent may be administered before or after the symptoms of hepatic dysfunction are developed, either continuously or intermittently.
- the functional food for preventing or suppressing hepatic dysfunction according to the present invention contains the agent for preventing or suppressing hepatic dysfunction of the present invention.
- the functional food may be functional food, such as foods for specified health uses, claiming prevention or suppression of hepatic dysfunction, such as hepatocellular necrosis.
- the functional food may optionally contain additives, such a sugars, proteins, lipids; vitamins, minerals, flavoring agents, or mixtures thereof. Further, the milk components from which the whey is separated, may also be contained.
- the content of the whey as the active component may suitably be selected depending on the form or kind of the food.
- the content may suitably be selected also depending on the continuity of intake of the functional food or the like factors, and is not particularly limited.
- a suitable content may be usually 1 to 100 mass %.
- the functional food may be in the form of, for example, fermented milk products, such as yogurt or lactic acid bacteria beverage, processed food and beverage containing whey, dry powders, tablets, capsules, granules, or the like.
- fermented milk products such as yogurt or lactic acid bacteria beverage
- processed food and beverage containing whey, dry powders, tablets, capsules, granules, or the like.
- the dose and the timing of administration of the functional food of the present invention are not particularly limited, and it is preferred to take the functional food in such an amount that the above-mentioned dose of the active component is generally achieved.
- the present functional food may be taken continuously or intermittently before or after the symptoms of hepatic dysfunction are developed.
- skim milk was dissolved in distilled water at a solid content of 9 mass %, subjected to high temperature pasteurization in an autoclave at 105° C. for 10 minutes, allowed to cool to the room temperature, inoculated with 3 mass % of a Lactobacillus helveticus CM4 starter, and cultured at 37° C. for 24 hours, to thereby centrifuged at 12000 G for 20 minutes for removing the solids, to prepare fermented milk whey.
- Example 1 Each of the obtained fermented milk whey (Example 1) and case in whey (Example 2) was diluted with distilled water to 10 mass %, and used in the following animal test as a drinking water. As a control, distilled water without whey was also used in the test.
- mice at 3 weeks of age were divided into three groups of 10 animals each, and allowed free access to solid feed (trade name MF, manufactured by ORIENTAL YEAST CO., LTD.), and distilled water, 10 mass % fermented milk whey prepared above, or 10 mass % caseln whey prepared aboveg for 1 month.
- the mice were then fastened for 18 hours, and each group was subdivided into two subgroups of 5 animals each.
- the mice were intraperitoneally administered with saline or acetaminophene solution (700 mg/kg). Acetaminophene is used as an antipyretic/analgesic even in popular medicines.
- the serum GOT and GPT levels were measured 2 and 4 hours after the administration using Transamirase CII Test Kit (WAKO PURE CHEMICAL INDUSTRIES, LTD.) for evaluating the effect of preventing or suppressing hepatic dysfunction.
- the results are shown in Table 1.
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Abstract
The present invention provides an agent for preventing or suppressing hepatic dysfunction which may be taken daily and continuously, has excellent safety, and is capable of effectively preventing and/or suppressing hepatic dysfunction, such as hepatocellular necrosis, and functional food, such as foods for specified health uses, for preventing or suppressing hepatic dysfunction containing this agent. The agent for preventing or suppressing hepatic dysfunction of the present invention contains whey as the active component, and the functional food for preventing or suppressing hepatic dysfunction contains the agent for preventing or suppressing hepatic dysfunction.
Description
- The present invention relates to an agent for preventing or suppressing hepatic dysfunction, and functional food, such as foods for specified health uses, for preventing or suppressing hepatic dysfunction. In particular, the present invention relates to an agent and functional food for preventing or suppressing hepatic dysfunction, which suppress the elevation of serum GOT and GPT levels caused by hepatocellular necrosis to prevent and/or suppress hepatic dysfunction.
- Liver is a central organ of metabolism, and has a variety of important functions, such as biligenesis, excretion, detoxication, and the like. On the other hand, liver is said to be a silent organ due to its great reserve, and hardly develops symptoms, such as malaise, jaundice, edema, and ascites, so that its dysfunction tends to be perceived too late. It is generally known that abundance of GOT (glutamic-oxaloacetic transaminase) and GPT (glutamic-pyruvic transaminase) are present in liver, and the blood GOT and OPT levels sensitively reflect the degree of hepatocellular necrosis, so that these levels are often used as convenient means for evaluating hepatic dysfunction.
- Recent westernization of dietary habit, nutritional unbalance, and ingestion of alcohol or drugs have imposed increasing burden on liver, resulting in substantial increase in the number of patients suffering from fatty liver. Chronic liver diseases progress through repeated hepatocellular destruction and regeneration over years to hepatocellular carcinoma. Patients suffering from such disease are also increasing.
- There is no effective drug for liver diseases at present, and diet therapy and rest are the prevailing therapy. Though, for example, glycyrrhizin formulation, such as Stronger Neo-Minophagen C (registered trade mark, manufactured by MINOPHAGEN PHARMACEUTICAL, CO., LTD.) is sometimes used for chronic liver diseases, such glycyrrhizin formulation is inactivated in the intestines, so that desired effect cannot be expected through oral administration, and parenteral injection is the main route of administration. Thus patients suffer from regular injections, and even side effects, such as hypertension or hypokalemia, are reported to be produced.
- On the other hand, various amino acid formulations are sometimes used for the purpose of ameliorating hepatic encephalopathy or hypoalbuminemia associated with liver diseases such as cirrhosis or hepatic insufficiency. However, such amino acid formulations are used with mere expectation of improvement in nutritional deficiency caused by liver diseases, i.e., improvement in nitrogen metabolism or reduction of blood ammonia level by balancing the plasma amino acid, rather than treatment of liver diseases.
- There has recently been proposed an agent for improving liver function containing lactoperoxidase and/or lactoferrin as an active component (see Patent Publication 1). Lactoferrin is known to be contained in milks of various mammals.
- However, lactoferrin is prone to thermal denaturation, and known to be denatured easily in ordinary high temperature pasteurization or the like process (see, for example, Non-patent Publications 1 to 3). Thus isolation or use of lactoferrin in industrial scale is restricted, and problems remain in cost and versatility.
- Whey has recently come to be known to contain various components having physiological functions, such as components for protecting gastric mucosa (α-lactalbumin) However, no improving effect on liver function has been reported of milk or whey that has undergone ordinary
- Patent Publication 1: JP-2001-226289-A
- Non-patent Publication 1: Shokuhin Shinsozai Yuukou Riyou
- Gijutsu Series “Lactoferrin” (March 2000, Shadan Houjin Kashi Sougou Gijutsu Center)
- Non-patent Publication 2: Nyugyo Gijutsu, Vol. 51, 2001, “Miruku no Rakutoferin (Lactoferrin in Milk)”
- Non-patent Publication 3: Journal of Dairy Science Vol. 74, No. 1, pG5-71, 1991
- It is an object of the present invention to provide an agent for preventing or suppressing hepatic dysfunction which may be taken daily and continuously, has excellent suppressing hepatic dysfunction, such as hepatocellular necrosis, and functional food, such as foods for specified health uses, for preventing or suppressing hepatic dysfunction containing this agent.
- According to the present invention, there is provided an agent for preventing or suppressing hepatic dysfunction comprising whey as an active component.
- According to the present invention, there is also provided functional food for preventing or suppressing hepatic dysfunction comprising the above agent for preventing or suppressing hepatic dysfunction.
- According to the present invention, there is provided a method for preventing or suppressing hepatic dysfunction in need thereof an effective amount of an agent for preventing or suppressing hepatic dysfunction comprising whey as an active component.
- According to the present invention, there is also provided use of whey for the manufacture of an agent for preventing or suppressing hepatic dysfunction.
- According to the present invention, there is further provided use of whey for the manufacture of functional food for preventing or suppressing hepatic dysfunction.
- Since the agent for preventing or suppressing hepatic dysfunction according to the present invention contains whey, which has been taken as food, as the active component, the agent may be taken daily and continuously, is excellently safe, and may effectively prevent and/or suppress hepatic dysfunction, such as hepatocellular necrosis. Since the functional food for preventing or suppressing hepatic dysfunction according to the present invention contains the present agent for preventing or suppressing hepatic dysfunction, the present functional food may be expected to prevent and/or suppress hepatic dysfunction.
- The present invention will now be explained in detail.
- The agent for preventing or suppressing hepatic dysfunction according to the present invention contains whey as the active component, and is capable of effectively preventing and/or suppressing, for example, the elevation of blood GOT and GPT levels which is said to be ascribable mainly to hepatocellular necrosis.
- The active component, whey, includes an aqueous fraction of milk obtained by removing all or most of the casein protein and the like from milk according to a common procedure, and may be, for example, acid whey and/or cheese whey. Examples of the acid whey may include fermented milk whey obtained by fermentation of milk with lactic acid bacteria, and casein whey containing an aqueous fraction of milk obtained by adding acid to milk to remove all or most of the casein protein and the like according to a common procedure. Fermented milk whey is particularly preferred for its excellent ability to prevent and/or suppress hepatic dysfunction.
- The fermented milk whey may usually be a fermented milk whey prepared by fermentation of milk with lactic acid bacteria, or by symbiotic fermentation of milk with lactic acid bacteria and a yeast. The starting material milk may be animal milk, such as cow's milk, goat's milk, or sheep's milk; vegetable milk, such as soy bean milk; or processed milk thereof, such as skim milk, reconstituted milk, powdered milk, or condensed milk. The milk may be in the form of a mixture.
- The solid content of the milk is not particularly limited For example, for skim milk, the solid non-fat content is typically about 9 mass %. On the other hand, considering the per-plant productivity, the solid non-fat content may be increased to some extent. The fermented milk whey obtained in the production of fermented milk may be separated from other milk components before use, but when the fermented milk whey is to be made into the functional food or the like to be discussed later, such other milk components are not necessarily separated.
- The lactic acid bacteria may be chose of the genus Streptococcus, Lactococcus, Lactobacillus, Bifidobacterium, or the like, with Lactobacillus being preferred. Specific examples of Lactobacillus may include Lactobacillus bulgaricus, Lactobacillus helveticus, Lactobacillus casei, Lactobacillus acidophilus, and Lactobacillus fermentum, with Lactobacillus heiveticus being particularly preferred. More specifically, Lactobacllius helveticus ATCC 15009, Lactobacillus heiveticus ATCC 521, and Lactobacillus helveticus CM4 strain (deposited at National Institute of Advanced Industrial Science and Technology, International Patent Organism Depositary under Accession Number FERM BP-6060 on Aug. 15, 1997) (referred to as CM4 hereinbelow) may be used, with CM4 being particularly preferred. CM4 has been deposited under the above-mentioned accession number under the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure. All restrictions on the availability to the public of this strain will be irrevocably removed upon the granting of a patent.
- The lactic acid bacteria are preferably in the form of a pre-cultured starter having sufficiently high activity. The initial cell count may preferably be about 105-107 cells/ml.
- When the fermented milk whey is to be used in functional food, such as foods for specified health uses, yeast may be used for symbiotic fermentation for improved flavor and palatability. The strain of the yeast is not particularly limited, and may preferably be, for example, yeast of the genus Saccharomyces, such as Saccharomyces cerevisiae. The content of the yeast may suitably be selected depending on the purpose.
- The fermentation may be carried out by culturing one or more kinds of the lactic acid bacteria in a medium, or culturing a mixture of one or more kinds of the lactic acid bacteria and one or more kinds of the yeast in a medium. The medium may be those composed only of one or more kinds of the milk components mentioned above, or those optionally contain additional components, such as yeast extract; vitamins, e.g. ascorbic acid; amino acids, e.g. cysteine; salts, e.g. sodium chloride; sugars, e.g. glucose, sucrose, raffinose, or stachyose; stabilizers, e.g. gelatine; and flavoring agents.
- The fermentation may be performed usually by static or stirred culture, for example at 20 to 50° C., preferably 30 to 45° C., at the initial pH of 6.0 to 7.0, and may be terminated when the cell count becomes 107 cells/ml or higher at pH 5.0 or lower. The milk may be subjected to high-temperature pasteurization before fermentation.
- The fermented milk whey may be separated from curd by means of a common separating operation. On the other hand, when the fermented milk whey as the active component is to be used in the functional food to be discussed later, the fermented milk containing the whey may be used as it is without separation, if so desired, or the extent of separation may suitably be decided.
- The casein whey may be prepared by, when solid milk, such as whole milk or skim milk is used, dissolving the milk in distilled water, adding, for example, lactic acid, citric acid, acetic acid, tartaric acid, fumaric acid, malic acid, aluconic acid, or adipic acid to adjust the acidity to a level suitable for removing protein, typically casein, and separating the whey component (aqueous fraction) by a common procedure, such as membrane filtration. Here, the milk may be subjected to high temperature pasteurization before the acid is added. The acid may usually be added in an amount for achieving 1.0 to 4.0% acidity, depending on the kind of the acid or the like.
- The cheese whey may be prepared in the ordinary cheese production, by coagulating milk with rennet to form curd, and separating the whey component from the curd by centrifugation or the like. Here, the milk may be subjected to high temperature pasteurization before the rennet is added.
- The dose of the whey as the active component in the present agent for preventing or suppressing hepatic dysfunction is not particularly limited, taking the continuity of administration into account, and may usually be not less than 0.001 g per kg body weight per day, preferably not less than 0.01 g per kg body weight per day, in terms of freeze-dried powder. Further, the agent for preventing or suppressing hepatic dysfunction of the present invention may optionally contain components other than the whey as desired, having the function of preventing or suppressing hepatic dysfunction.
- The agent for preventing or suppressing hepatic dysfunction according to the present invention may be in a whey concentrate obtained by concentrating whey through vacuum concentration or the like process, or a dried whey powder obtained by drying whey through freeze-drying or spray drying.
- The agent for preventing or suppressing hepatic dysfunction according to the present invention may be administered usually through an oral route. For example, the agent may be administered before or after the symptoms of hepatic dysfunction are developed, either continuously or intermittently.
- The functional food for preventing or suppressing hepatic dysfunction according to the present invention contains the agent for preventing or suppressing hepatic dysfunction of the present invention.
- The functional food may be functional food, such as foods for specified health uses, claiming prevention or suppression of hepatic dysfunction, such as hepatocellular necrosis.
- The functional food may optionally contain additives, such a sugars, proteins, lipids; vitamins, minerals, flavoring agents, or mixtures thereof. Further, the milk components from which the whey is separated, may also be contained.
- In the functional food of the present invention, the content of the whey as the active component may suitably be selected depending on the form or kind of the food. The content may suitably be selected also depending on the continuity of intake of the functional food or the like factors, and is not particularly limited. A suitable content may be usually 1 to 100 mass %.
- The functional food may be in the form of, for example, fermented milk products, such as yogurt or lactic acid bacteria beverage, processed food and beverage containing whey, dry powders, tablets, capsules, granules, or the like.
- The dose and the timing of administration of the functional food of the present invention are not particularly limited, and it is preferred to take the functional food in such an amount that the above-mentioned dose of the active component is generally achieved. For example, the present functional food may be taken continuously or intermittently before or after the symptoms of hepatic dysfunction are developed.
- The present invention will now be explained in more detail with reference to Examples, which do not intend to limit the present invention.
- Commercially available skim milk was dissolved in distilled water at a solid content of 9 mass %, subjected to high temperature pasteurization in an autoclave at 105° C. for 10 minutes, allowed to cool to the room temperature, inoculated with 3 mass % of a Lactobacillus helveticus CM4 starter, and cultured at 37° C. for 24 hours, to thereby centrifuged at 12000 G for 20 minutes for removing the solids, to prepare fermented milk whey.
- On the other hand, commercially available skin milk was dissolved in distilled water at a solid content of 9 mass %, subjected to high temperature pasteurization in an autoclave at 105° C. for 10 minutes, and allowed to cool to the room temperature. Lactic acid was added to increase the acidity to 2.2%. Then the product was centrifuged at 12000 G for 20 minutes for removing the solids, to prepare casein whey.
- Each of the obtained fermented milk whey (Example 1) and case in whey (Example 2) was diluted with distilled water to 10 mass %, and used in the following animal test as a drinking water. As a control, distilled water without whey was also used in the test.
- Male ICR mice at 3 weeks of age were divided into three groups of 10 animals each, and allowed free access to solid feed (trade name MF, manufactured by ORIENTAL YEAST CO., LTD.), and distilled water, 10 mass % fermented milk whey prepared above, or 10 mass % caseln whey prepared aboveg for 1 month. The mice were then fastened for 18 hours, and each group was subdivided into two subgroups of 5 animals each. The mice were intraperitoneally administered with saline or acetaminophene solution (700 mg/kg). Acetaminophene is used as an antipyretic/analgesic even in popular medicines. However, it is known that acetaminophine, if administered in an excess amount, cannot be processed in liver, resulting in fulminant hepatitis-like hepatic dysfunction. Thus this drug is often used in experiments for evaluation of hepatic dysfunction.
- The serum GOT and GPT levels were measured 2 and 4 hours after the administration using Transamirase CII Test Kit (WAKO PURE CHEMICAL INDUSTRIES, LTD.) for evaluating the effect of preventing or suppressing hepatic dysfunction. The results are shown in Table 1.
- It is understood from the results in Table 1 that in the control group given distilled water, the serum GOT and GPT levels were remarkably elevated by administration of acetaminophene, whereas in the groups given the fermented milk whey or the case in whey, such elevation was suppressed, so that excellent effect of preventing or suppressing hepatic dysfunction was exhibited. It was particularly noted that, in the group given the fermented milk whey, elevation of the GOT and GPT levels by administration of acetaminophene was suppressed more remarkably than in the group given the casein whey.
TABLE 1 Level Level after after 2 hours 4 hours GOT Control Group given water + saline 164 198 level Group given water + 577 841 acetaminophene Example 1 Group given fermented milk 83.9 59 whey + saline Group given fermented milk 125 229 whey + acetaminophene Example 2 Group given casein whey + 123 212 saline Group given casein whey + 340 798 acetaminophene GPT Control Group given water + saline 11.8 28.4 level Group given water + 128 618 acetaminophene Example 1 Group given fermented milk 6.29 15.8 whey + saline Group given fermented milk 6.02 30.1 whey + acetaminophene Example 2 Group given casein whey + 14.6 20.5 saline Group given casein whey + 40.5 110 acetaminophene
Claims (10)
1. An agent for preventing or suppressing hepatic dysfunction comprising whey as an active component.
2. The agent for preventing or suppressing hepatic dysfunction according to claim 1 , wherein said whey is at least one of acid whey and cheese whey.
3. The agent for preventing or suppressing hepatic dysfunction according to claim 2 , wherein said acid whey comprises fermented milk whey obtained by fermentation of milk with bacteria including lactic acid bacteria.
4. The agent for preventing or suppressing hepatic dysfunction according to claim 3 , wherein said lactic acid bacteria are of the genus Lactobacillus sp.
5. The agent for preventing or suppressing hepatic dysfunction according to claim 4 , wherein said lactic acid bacteria of the genus Lactobacillus are of the species Lactobacillus helveticus.
6. The agent for preventing or suppressing hepatic dysfunction according to claim 5 , wherein said Lactobacillus helveticus is of a strain Lactobacillus helveticus CM4 (deposited at National Institute of Advanced Industrial Science and Technology, International Patent Organism Depositary under Accession Number FERM BP-6060).
7. The agent for preventing or suppressing hepatic dysfunction according to claim 2 , wherein said acid whey is casein whey containing an aqueous fraction obtained by adding to milk.
8. Functional food for preventing or suppressing hepatic dysfunction comprising an agent for preventing or suppressing hepatic dysfunction according to any one of claims 1 to 7 .
9. The functional food according to claim 8 , further comprising milk components other than whey.
10. The agent for preventing or suppressing hepatic dysfunction according to claim 5 or 6 , wherein said hepatic dysfunction is drug-induced hepatitis.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004-106105 | 2004-03-31 | ||
| JP2004106105 | 2004-03-31 | ||
| PCT/JP2005/006243 WO2005094848A1 (en) | 2004-03-31 | 2005-03-31 | Agent for preventing or suppressing hepatopathy and functional food for preventing or suppressing hepatopathy |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2005/006243 A-371-Of-International WO2005094848A1 (en) | 2004-03-31 | 2005-03-31 | Agent for preventing or suppressing hepatopathy and functional food for preventing or suppressing hepatopathy |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/952,822 Continuation US7785633B2 (en) | 2004-03-31 | 2007-12-07 | Agent for preventing or suppressing hepatopathy and functional food for preventing or suppressing hepatopathy |
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| Publication Number | Publication Date |
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| US20070224285A1 true US20070224285A1 (en) | 2007-09-27 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/599,447 Abandoned US20070224285A1 (en) | 2004-03-31 | 2005-03-31 | Agent for Preventing or Suppressing Hepatopathy and Functional Food for Preventing or Suppressing Hepatopathy |
| US11/952,822 Expired - Fee Related US7785633B2 (en) | 2004-03-31 | 2007-12-07 | Agent for preventing or suppressing hepatopathy and functional food for preventing or suppressing hepatopathy |
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| Application Number | Title | Priority Date | Filing Date |
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| US11/952,822 Expired - Fee Related US7785633B2 (en) | 2004-03-31 | 2007-12-07 | Agent for preventing or suppressing hepatopathy and functional food for preventing or suppressing hepatopathy |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US20070224285A1 (en) |
| EP (1) | EP1736164A4 (en) |
| JP (1) | JP4947636B2 (en) |
| CN (1) | CN101039685B (en) |
| TW (1) | TW200536552A (en) |
| WO (1) | WO2005094848A1 (en) |
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| JP5804542B2 (en) * | 2010-03-25 | 2015-11-04 | 雪印メグミルク株式会社 | Fatty liver prevention and / or inhibitor |
| CN110241046B (en) * | 2019-06-26 | 2021-05-18 | 河北一然生物科技有限公司 | Lactobacillus helveticus capable of relieving alcoholic liver injury and application thereof |
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| US5710132A (en) * | 1993-11-04 | 1998-01-20 | Biotest Pharma Gmbh | Use of bovine colostral milk as a preparation for the protection of the liver |
| US6225104B1 (en) * | 1996-03-11 | 2001-05-01 | Renata Maria Anna Cavaliere Vesely | Strains of bacteria and pharmaceutical composition containing one or more of such strains and use of same for preventing and treating diseases associated with or caused by altered metabolism of bile acids |
| US6262019B1 (en) * | 1998-04-30 | 2001-07-17 | Vit-Immune, L. C. | Method of treatment of glutathione deficient mammals |
| US6534304B1 (en) * | 1997-09-26 | 2003-03-18 | Calpis Co., Ltd. | Lactobacillus helveticus bacterium having high capability of producing tripeptide, fermented milk product, and process for preparing the same |
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| JPH01198978A (en) | 1988-02-01 | 1989-08-10 | Eiko Otaka | Overhead parking area device |
| JP2764267B2 (en) * | 1988-04-20 | 1998-06-11 | 雪印乳業株式会社 | Functional food and drink with bile acid secretion promoting action |
| JP2862418B2 (en) * | 1990-09-20 | 1999-03-03 | 森永乳業株式会社 | Functional foods effective for improving lipid metabolism |
| JP2944008B2 (en) * | 1990-09-20 | 1999-08-30 | 森永乳業株式会社 | Parenteral lipid metabolism improver |
| JPH08999A (en) | 1994-04-20 | 1996-01-09 | Riken Corp | Exhaust gas purifying material and exhaust gas purifying method |
| JPH0899888A (en) * | 1994-09-30 | 1996-04-16 | Snow Brand Milk Prod Co Ltd | Glutathione peroxidase activator |
| SE9501719D0 (en) * | 1995-05-09 | 1995-05-09 | Probi Ab | Pharmaceutical composition |
| JP4053107B2 (en) | 1996-02-01 | 2008-02-27 | 中外製薬株式会社 | Preventive and therapeutic agents for thrombocytopenia |
| JPH09301877A (en) * | 1996-05-13 | 1997-11-25 | Youshindou:Kk | Agent for treatment and prevention of hepatitis |
| JP4163276B2 (en) * | 1998-02-05 | 2008-10-08 | 独立行政法人理化学研究所 | Functional composition |
| JP3958456B2 (en) * | 1998-12-25 | 2007-08-15 | 高梨乳業株式会社 | Functional food and drink with serum lipid improving effect |
| JP2000197469A (en) * | 1999-01-08 | 2000-07-18 | New Food Creation Gijutsu Kenkyu Kumiai | Functional food and drink with serum lipid improving effect |
| FI113741B (en) | 1999-11-01 | 2004-06-15 | Valio Oy | Process for the preparation of a product containing peptides with antihypertensive effect |
| JP4679687B2 (en) * | 2000-02-16 | 2011-04-27 | 雪印乳業株式会社 | Liver function improving agent |
| CN1287855C (en) * | 2000-11-30 | 2006-12-06 | 森永乳业株式会社 | Remedies for chronic hepatitis B |
| KR100375335B1 (en) | 2001-01-17 | 2003-03-06 | 한국과학기술연구원 | A Method for Depositing Diamond Films Without Fracture by a Control of Substrate Temperatures Using Powders |
| JP3853673B2 (en) * | 2001-03-09 | 2006-12-06 | 森永乳業株式会社 | Treatment for chronic hepatitis C |
| SE0201214D0 (en) * | 2002-04-23 | 2002-04-23 | Jafar Mahdavi | Multicultural fermented yogurt |
| TWI317636B (en) * | 2002-11-22 | 2009-12-01 | Meiji Dairies Corp | Nutritional compositions for liver disease patients or for patients underhigh levels of invasive stress |
-
2005
- 2005-03-31 US US10/599,447 patent/US20070224285A1/en not_active Abandoned
- 2005-03-31 CN CN2005800172416A patent/CN101039685B/en not_active Expired - Fee Related
- 2005-03-31 EP EP05727951A patent/EP1736164A4/en not_active Withdrawn
- 2005-03-31 TW TW094110309A patent/TW200536552A/en unknown
- 2005-03-31 JP JP2006511784A patent/JP4947636B2/en not_active Expired - Fee Related
- 2005-03-31 WO PCT/JP2005/006243 patent/WO2005094848A1/en not_active Ceased
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5710132A (en) * | 1993-11-04 | 1998-01-20 | Biotest Pharma Gmbh | Use of bovine colostral milk as a preparation for the protection of the liver |
| US6225104B1 (en) * | 1996-03-11 | 2001-05-01 | Renata Maria Anna Cavaliere Vesely | Strains of bacteria and pharmaceutical composition containing one or more of such strains and use of same for preventing and treating diseases associated with or caused by altered metabolism of bile acids |
| US6534304B1 (en) * | 1997-09-26 | 2003-03-18 | Calpis Co., Ltd. | Lactobacillus helveticus bacterium having high capability of producing tripeptide, fermented milk product, and process for preparing the same |
| US6262019B1 (en) * | 1998-04-30 | 2001-07-17 | Vit-Immune, L. C. | Method of treatment of glutathione deficient mammals |
Also Published As
| Publication number | Publication date |
|---|---|
| US7785633B2 (en) | 2010-08-31 |
| JP4947636B2 (en) | 2012-06-06 |
| EP1736164A1 (en) | 2006-12-27 |
| EP1736164A4 (en) | 2009-06-24 |
| JPWO2005094848A1 (en) | 2008-02-14 |
| CN101039685B (en) | 2010-06-16 |
| WO2005094848A1 (en) | 2005-10-13 |
| US20080085321A1 (en) | 2008-04-10 |
| CN101039685A (en) | 2007-09-19 |
| TW200536552A (en) | 2005-11-16 |
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