WO2007010976A1 - Body weight gain inhibitory composition comprising d-psicose and use thereof - Google Patents
Body weight gain inhibitory composition comprising d-psicose and use thereof Download PDFInfo
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- WO2007010976A1 WO2007010976A1 PCT/JP2006/314366 JP2006314366W WO2007010976A1 WO 2007010976 A1 WO2007010976 A1 WO 2007010976A1 JP 2006314366 W JP2006314366 W JP 2006314366W WO 2007010976 A1 WO2007010976 A1 WO 2007010976A1
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- Prior art keywords
- psicose
- obesity
- composition
- overweight
- body weight
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7004—Monosaccharides having only carbon, hydrogen and oxygen atoms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
Definitions
- the present invention relates to the use of D-psicose to suppress weight gain and / or to reduce overweight. More specifically, the present invention can suppress excessive weight gain due to various causes, reduce overweight, prevent and reduce obesity, and prevent excessive weight gain or overweight.
- the present invention relates to a composition, food, food material, food additive, beverage, drinking water, drug, drug substance, and feed containing D-psicose and / or a derivative thereof suitable for a person and / or animal.
- the present invention also relates to a method for suppressing weight gain and / or reducing overweight due to various causes.
- rare sugars exist in nature, the abundance is extremely small. Rare sugars are divided into aldoses, ketoses and alcohols by chemical structure. Examples of aldoses include D-alose strength. Examples of ketoses include D-psicose strength. Examples of alcohols include aritol. However, since most of these rare sugars have been difficult to obtain because they were not mass-produced in the past, little research has been conducted on their physiological and pharmacological activities. Recently, a large-scale production method using enzymes was developed by Prof. Irimori et al., Faculty of Agriculture, Kagawa University, and some rare sugars such as D-psicose, D-allose, and aritol were produced. Research is progressing.
- Non-patent Document 1 suppression of D-Glucose transport in the isolated intestinal tract (Non-patent Document 1), promotion of insulin secretion from rat spleen j8 cell line (Patent Document 1), vascular endothelial cells Suppression of MCP-1 secretion from strains (Patent Document 1), etc., and in vivo experiments, body fat accumulation mitigating action (Non-Patent Document 2), and not becoming energy in vivo (Non-Patent Document 3), etc.
- Non-Patent Document 1 suppression of D-Glucose transport in the isolated intestinal tract
- Patent Document 1 promotion of insulin secretion from rat spleen j8 cell line
- Patent Document 2 vascular endothelial cells Suppression of MCP-1 secretion from strains
- Non-Patent Document 2 body fat accumulation mitigating action
- Non-patent Document 1 suppression of D-glucose transport in the isolated intestinal tract (Non-patent Document 1), promotion of insulin secretion from the rat spleen j8 cell line (Patent Document 1), vascular endothelial cells Suppression of MCP-1 secretion from strains (Patent Document 1), action to suppress the accumulation of neutral fat in adipocytes (Non-Patent Documents 2 and 3), etc. Reference 4), and the energy in the living body, which is not unique (Non-Patent Document 5), have been clarified.
- Non-Patent Document 1 Fiscal 1999 Science and Technology Comprehensive Research Commission Regional Lead Research Research Result Report “Study on Mechanisms of Action of Rare Sugars as Pharmaceuticals” Kagawa Medical University, Masaaki Tokuda, Yoshishi Konishi, Maeda Tsuji, 2000
- Non-Patent Document 2 2005 Japanese Biochemical Society Abstract (Kobe) “Effect of monosaccharides on fat cells” Kagawa University School of Medicine, Madoka Saito and 4 others.
- Non-Patent Document 3 2006 International Biochemical Society Abstract (Kyoto) “Effects of Rare Sugars on the Properties of 3T3—LI Adipocytes.”
- Non-patent document 4 Fiscal 1999 Science and Technology Comprehensive Research Commission Regional Leading Research Research Results Report “Nutritional Evaluation of Rare Sugars Using Rats and Their Application to Food” Kagawa University Faculty of Agriculture, Hiroo Suzuki, Matsuo Tatsuhiro, Hashiguchi Mineo, 2000
- Non-Patent Document 5 Fiscal 2000 Science and Technology Research Fund Regional Lead Research Research Results Report “Nutritional Evaluation of Rare Sugars Using Rats and Application to Food” Kagawa University Faculty of Agriculture, Hiroo Suzuki, Matsuo Tatsuhiro, Hashiguchi Mineo, 2001
- Patent Document 1 International Publication Number W003 / 097820
- D-psicose is a sugar with a refreshing sweetness that is about 60% stronger than sucrose, and abnormal sugar metabolism is closely related to abnormal fat metabolism, so this rare sugar has an anti-obesity effect The potential is great. Therefore, we investigated the anti-obesity effect of D-psicose using human obesity model animals.
- the purpose of the present invention based on the results of the above studies is to achieve D-psicose and / or suitable for humans and animals that are capable of suppressing overweight and reducing overweight, and that require prevention of obesity and improvement of obesity.
- the present invention provides a composition, a food, a food material, a food additive, a beverage, drinking water, a drug, a pharmaceutical raw material, a feed and the like containing the derivative.
- Another object of the present invention is to provide a method for suppressing an excessive increase in body weight due to various causes and reducing an overweight.
- the present invention includes D-psicose, and suppresses excessive weight gain and / or A gist is a composition characterized by reducing overweight.
- D-psicose power is formulated to include ⁇ 90% by weight
- the present invention includes D-psicose and is formulated to include D-psicoseca ⁇ -90% by weight.
- the gist of the present invention is a composition characterized in that it suppresses and / or reduces overweight.
- D-psicose is D-psicose and Z or a derivative thereof
- the present invention contains D-psicose and Z or a derivative thereof, preferably formulated so that D-psicose and Z or a derivative thereof is contained in an amount of 90 to 90% by weight.
- the gist of the present invention is a composition characterized in that it suppresses overweight and / or reduces overweight.
- the present invention is characterized in that any of the above-described yarns and adults is used for a person and Z or an animal who need to suppress overweight and / or reduce overweight.
- the gist is a method of suppressing overweight and / or reducing overweight.
- the gist of the present invention is a composition comprising D-psicose and characterized by preventing obesity and improving Z or obesity status.
- D-psicose strength is formulated to include 90% by weight
- the present invention includes D-psicose, which is formulated to include D-psicose ca ⁇ -90% by weight, to prevent obesity.
- a thread and composition characterized by improving Z and obesity status.
- D-psicose is D-psicose and Z or a derivative thereof
- the present invention contains D-psicose and Z or a derivative thereof, preferably formulated so that D-psicose and Z or a derivative thereof is contained in an amount of 90 to 90% by weight.
- the gist of the present invention is a composition characterized by preventing obesity and improving Z or obesity status.
- the present invention also provides a method for preventing and preventing obesity, characterized by using any of the compositions described above for people and Z or animals that require prevention of obesity and improvement of Z or obesity status.
- the gist is a method for improving an obesity state.
- the present invention comprises D-psicose and / or a derivative thereof as an active ingredient, and an excess of body weight.
- a composition having an inhibitory effect on increase and / or an effect of reducing overweight and / or a composition having an effect of preventing obesity due to various causes and / or an effect of improving obesity, and these compositions are used. It is possible to provide a method for suppressing overweight and / or reducing overweight and / or a method for preventing and / or improving obesity by various causes.
- the present invention is characterized in that it suppresses excess body weight gain and / or reduces overweight, and comprises D-psicose and / or a derivative thereof as an active ingredient, for foods, health foods, and patients.
- the present invention uses a composition containing D-psicose and / or a derivative thereof to suppress overweight and / or reduce overweight and / or prevent obesity caused by various causes.
- a method for improving obesity can be provided.
- FIG.l Effect of repeated administration of D-Psicose on body weight of Zucker (fa / fa) rats [In the figure, *; p ⁇ 0.05, * *; p ⁇ 0.001 (vs distilled water administration group) ⁇ .
- FIG. 2 shows the effect of D-Psicose on the body weight of mice administered with Aurothioglucose (ATG) [in the figure, * *; p ⁇ 0.01 (vs ATG control group)].
- Aurothioglucose Aurothioglucose
- D-psicose With regard to D-psicose, in recent years, with the advent of epimerase (see, for example, JP-A-6-125776), for example, it has become possible to produce it from D-fructose, which is a monosaccharide abundant in nature. Although it is still expensive, it has become relatively easy to obtain. It was found that by using D-fructose as a raw material, the problem of raw material cost was solved and a hetero-oligosaccharide expected to have a new physiological activity based on D-psicose was obtained. Among monosaccharides, D-psicose is a hexasaccharide having a ketone group as a reducing group.
- D-psicose is known to have D and L isomers as optical isomers.
- D-psicose is a known substance but rarely exists in nature, so it is defined as “rare sugar” according to the definition of the International Association of Rare Sugars.
- Rare sugars can be defined as monosaccharides (aldoses, ketoses and sugar alcohols) that rarely exist in nature. Also in the present invention, it is a rare sugar based on the above definition, and preferably ketose D-psicose. This definition is ambiguous because it is not a definition of sugar structure or properties. That is, there is no definition of an amount such as a rare sugar that is less than a certain amount. However, there are six types of aldoses that are generally abundant in nature: D-glucose, D-galactose, D-mannose, D-ribose, D-xylose, and L-arabinose. Other aldoses are defined as rare sugars. Is done.
- ketose D-fructose exists, and other ketoses are rare sugars.
- Other ketoses include D-tagatose, D-sorbose, L-fructose, L-psicose, L-tagatose, and L-sorbose.
- Sugar alcohol can be produced by reducing monosaccharides, but D-sorbitol is relatively large in nature, but the others are quantitatively small, so these are also rare sugars.
- the rare sugar D-psicose used in the present invention has been developed as a method for mass production of rare sugars from monosaccharides existing in large quantities in nature. Can be manufactured.
- D-psicose derivative used in the present invention will be described.
- a compound obtained by converting the structure of a molecule from a certain starting compound by a chemical reaction is called a derivative of the starting compound.
- Derivatives of hexose containing D-psicose include sugar alcohols (when monosaccharides are reduced, aldehyde groups and ketone groups become alcohol groups and polyhydric alcohols of the same number as carbon atoms), uronic acid ( It is an oxidized monosaccharide alcohol group.
- D-glucuronic acid, galacturonic acid, and mannuronic acid are known.
- Amino sugar substituted with OH group NH2 group of sugar molecule, darcosamine, chondrosamine) , Glycosides, etc. are common, but are not limited thereto.
- D-psicose is considered to be less toxic to animals, with no reported toxicity to humans.
- D-psicose is a sugar with a refreshing sweetness that dissolves in water and is about 60% stronger than sucrose. The sweetness is refined and refreshing, and it resembles the sweetness of fratatose rather than the discomfort associated with bitterness and astringency like saccharin.
- D-psicose is in harmony with other tastes of various substances such as acidity, salt to taste, astringency, umami, bitterness, etc., for sweetening and taste improvement of ordinary foods and beverages, quality improvement, etc. Can be advantageously used.
- Compositions targeted by the present invention are edible containing D-psicose and / or its derivatives And / or is any medicinal composition.
- a composition containing D-psicose as an active ingredient also serves as a food additive, food material, food and drink, pharmaceutical / quasi-drug, and feed power to suppress overweight and / or reduce overweight.
- the group power is also selected. Utilizing the functionality of the composition, it became possible to develop healthy foods and drinks, foods with nutritional foods and drinks for patients, and feed for domestic animals such as livestock, poultry and fish.
- the food or drink is a functional food, a nutritional supplement, or a healthy food or drink for suppressing excessive increase in body weight and / or reducing overweight.
- the above feed is a feed for livestock, poultry and pets for suppressing excess weight gain and / or reducing overweight.
- the food material of the composition containing the above-mentioned D-psicose as an active ingredient can be used in any form of food, beverage or feed.
- composition containing D-psicose of the present invention as an active ingredient, its content is not particularly limited, but it depends on the degree of intended function, usage mode, usage amount, etc. It can be adjusted as appropriate, for example 0.05 to 100% by mass.
- the composition for suppressing overweight and / or reducing overweight can be used for the human body, other foods and drinks, pharmaceuticals, feeds, and external preparations for skin. In addition, it can be taken by mouth or applied to the skin.
- foods and drinks when blended in foods and drinks, foods and drinks can be provided for treating or preventing diseases that should suppress excess body weight gain and / or reduce overweight. From the prevention effect, it can be expected to be used as health food, nutritional food, etc. In addition, it can be used for livestock and feed or feed for Z or fish. By using it in the human body, other foods and drinks, pharmaceuticals, fertilizers, feeds, and external preparations for skin, it is possible to obtain an effect of treating or preventing an overweight and / or a disease that should reduce overweight. .
- D-psicose and / or a derivative thereof is usually blended so as to be contained in an amount of 0.1 to 50% by weight in the composition. Preferably it is 1-50 weight%, More preferably, it is 10-30 weight%. However, if the content is low, it is sufficient to increase the intake of the composition. If the content is high, if the content is low, the intake of the composition may be reduced. Therefore, with regard to the blending ratio, it can be used at a blending ratio close to the lower limit for ordinary foods and beverages. When used in pharmaceuticals, tablets and capsules, it can be used at a blending ratio close to the upper limit.
- the dosage should be determined by the individual's age, weight and symptoms, etc., but in many cases the effective dose is D-psicose per adult It is appropriate to take 1-50g in divided doses before meals, after meals or with meals.
- the dose of D-psicose and Z or its derivatives is preferably taken as an oral dose of 0.3 to 50 g daily for adults as D-psicose, but may be increased or decreased appropriately depending on age and symptoms. Is possible.
- the daily anti-obesity and Z or ameliorating agent of the present invention should be taken once a day, or divided into 2 or 3 times a day at an appropriate interval, or before, after or after meals. Is preferred.
- the composition of the present invention When used for foods, it is in a form as it is, a form diluted with oil, a milk form meal, or a form to which a carrier generally used in the food industry is added. It may be prepared.
- the beverage form is a non-alcoholic beverage or an alcoholic beverage.
- Non-alcoholic beverages include, for example, non-carbonated beverages such as carbonated beverages, fruit juice beverages, and nectar beverages, soft drinks, sports beverages, tea, coffee, cocoa, etc.
- the form of food can be mentioned.
- Main departure Examples of the use of the light composition as a food material or food additive for the purpose of improving the above abnormalities of carbohydrate metabolism and / or lipid metabolism include powders or granules dissolved in tablets, capsules, beverages, etc. Solids, semi-solids such as jelly, liquids such as drinking water, and high-concentration solutions used after dilution.
- the composition of the present invention can be appropriately added to foods to provide health foods or sick foods for the purpose of obesity prevention and Z
- vitamins, carbohydrates, pigments, fragrances and the like that are usually added to foods can be appropriately blended.
- the food can be eaten in any form, liquid or solid. It can be eaten as a soft capsule encapsulated by gelatin or the like.
- Capsules are made, for example, with a gelatin film prepared by adding water to raw gelatin and dissolving it, and then adding a plasticizer (such as glycerin or D-sorbitol).
- the food material and food additive of the present invention will be described. Since D-psicose is soluble in water, it can be easily added to beverages such as coffee and juice, confectionery, and various processed foods. Furthermore, the composition of the present invention can be appropriately added to foods and / or food materials to obtain processed foods for health and / or patients for the purpose of preventing obesity and / or improving obesity. .
- the composition of the present invention is used as a food material and / or a food additive for preparing food that can be eaten, taken or taken by a person and animals who need obesity prevention and / or improvement of obesity with a general meal. It can be used to prevent excessive weight gain, improve overweight, increase QOL, reinforce the effects of drugs or other foods used for similar purposes, and reduce the amount used. Can be reduced.
- the dosage should be determined by the individual's age, weight and symptoms, etc. In many cases, effective doses are rare sugars per day. It is appropriate to take -50g in divided doses before meals, after meals or with meals.
- the use form of the composition of the present invention as a food material or food additive for the purpose of preventing obesity and / or ameliorating obesity, etc. includes powders dissolved in tablets, capsules, beverages, etc. Solid agents such as granules, semi-solid bodies such as jelly, drinking water, etc. Liquid, high-concentration solution to be used after dilution. Furthermore, the composition of the present invention can be appropriately added to foods to provide health foods or sick foods for the purpose of preventing obesity and / or improving obesity.
- the drinking water of the present invention is a colorless and transparent, odorless, almost tasteless aqueous solution containing 1 to 5% by weight of D-psicose and / or a derivative thereof.
- the amount is preferably 1.5 to 4% by weight, more preferably 2 to 3% by weight. If it is less than 1% by weight, the effect of preventing obesity and / or improving the condition of obesity is not sufficient. If it exceeds 5% by weight, the sweetness derived from D-psicose, which has 60% sweetness of sugar, can be felt.
- This drinking water is colorless and transparent, and has a strong sweetness that smells. Therefore, it can be used as drinking water as it is, and can also be used for cooking rice, cooking, tea and coffee.
- the agent of the present invention will be described.
- the present inventor examined in detail the effect of D-psicose on the body weight of rats using genetic and experimental obesity model animals. As a result, we found that D-psicose has the effect of suppressing weight gain and reducing overweight.
- Drugs containing D-psicose and / or its derivatives as an active ingredient for the purpose of preventing obesity and / or improving obesity status are used alone or in general.
- Formulated with appropriate additives such as form, stabilizer, preservative, binder, disintegrant, liquid, granule, fine granule, powder, tablet, capsule, pill, ointment, patch, spray
- An appropriate dosage form such as an agent, spray or injection can be selected and formulated and administered orally, nasally, transdermally or intravenously.
- composition of the present invention When the composition of the present invention is applied clinically as a drug, D-psicose and / or a derivative thereof as an active ingredient is used as a solid, semi-solid or liquid pharmaceutical carrier such as a diluent, an excipient. It is desirable to prepare a preparation containing additives such as an agent and a stabilizer.
- the ratio of the active ingredient to the carrier component can vary between 1 and 90% by weight.
- the dosage form and mode of administration are liquids, granules, fine granules, powders, tablets, capsules, pills, ointments, patches, sprays, sprays or injections. Or it may be administered orally with the bulk. When used as a liquid, it may be administered nasally or intravenously in addition to oral administration.
- a pharmaceutical organic or organic solid, semi-solid or liquid carrier, solubilizer or diluent suitable for oral administration, nasal administration, transdermal administration or intravenous administration is used as a composition of the present invention. It can be used to prepare as a medicine. Water, gelatin, lactose, starch, magnesium stearate, talc, animal and vegetable oil benzyl alcohol, gum, polyalkylene glycol, petroleum oil, coconut oil, lanolin, or other carriers used in medicine All can be used as a carrier for a drug containing the composition of the present invention. In addition, stabilizers, moistening agents, emulsifiers, and salts for adjusting the osmotic pressure and maintaining the pH of the compounding agent can be appropriately used as auxiliary agents.
- the drug containing the composition of the present invention contains other pharmaceutically effective ingredients that can be appropriately administered together with the drug of the present invention in obesity prevention and / or improvement of obesity status. May be.
- the drug containing the composition of the present invention contains other pharmaceutically effective ingredients that can be appropriately administered together with the drug of the present invention in obesity prevention and / or improvement of obesity status. May be.
- the corresponding amount (ratio) is preferably 1 to 80% by weight.
- the clinical dose is preferably taken as an oral dose of 1 to 50 g daily for adults as D-psicose and / or its derivatives, but may be increased as appropriate depending on age, symptoms, etc. It can also be reduced.
- the daily dose of the agent of the present invention is preferably administered once a day or divided into two or more times at an appropriate interval, or before, after or with a meal.
- D-psicose and / or its derivative is used as a drug substance as a general excipient, stabilizer, preservative, It can also be used for purposes such as binders and disintegrants. Alternatively, for example, when obesity appears secondary, it is necessary to improve the obesity state in addition to the treatment of the causative disease.
- the product can also be used as a raw material for preparation as described above. In this case, the amount of D-psicose and / or its derivative used and the ratio with other drugs can be appropriately adjusted depending on the content or nature of these therapeutic agents in the preparation.
- Type of bait used in the experiment mouse “rat” hamster CE2 manufactured by Claire Japan
- Feeding method free intake
- fa / fa rats Ten-week-old male Zucker (fa / fa) rats (hereinafter referred to as Zuc (fa)) were used. These animals were administered in distilled water (control group), D-psicose 0.5 g / kg (P0.5), D-psicose lg / kg (Pl), D-psicose 2 g / kg. Group (P2), D-psicose 4g / kg group (P4), 5 groups Divided into. D-psicose was dissolved in distilled water and the administration volume was 10 mL / kg.
- the above D-psicose solution or distilled water was orally administered by gavage once a day.
- Body weight was measured at 3 or 4 day intervals. The measured values were expressed as mean values and standard errors, and were performed using a significant difference test or a Tukey multiple range test.
- mice 500 mg / kg was administered intraperitoneally.
- 7 mice died out of 60 mice administered ATG, and 53 mice survived.
- animals with a body weight greater than the mean value of the animals (non-ATG control group) that had not been administered ATG (non-ATG control group) + standard deviation X2 were regarded as experimentally fertile mice.
- the 53 surviving mice 26 were experimental obese mice.
- mice are divided into 3 groups: distilled water administration group (ATG control group), D-psicose 1% aqueous solution administration group (ATG + P1%) and D-psicose 10% aqueous solution administration group (ATG + P10%). It was. These D-psicose aqueous solution administration groups were given D-psicose aqueous solution from the 15th day to the 28th day of ATG administration and distilled water after the body weight measurement on the 18th day as drinking water.
- Body weight was measured at 3 or 4 day intervals. The measured values are expressed as average values and standard errors. 3 ⁇ 4, g, Test iiTukey multiple range test is used.
- the weight gain of animals in the D-psicose administration group was less than that in the control group.
- the body weight in the P4 group was significantly different from the control group at all measurement points after the 10th day of D-psicose administration.
- the P2 group showed significantly less body weight than the control group on day 21 after D-psicose administration (Fig. 1).
- the body weight of the animals in the ATG + P10% group decreased immediately after administration of D-psicose, and during the period of administration of D-psicose (from day 15 to day 28 of ATG administration), the body weight of the animals in the non-ATG control group There was no significant difference. Even after changing the drinking water from D-psicose 10% aqueous solution to distilled water on the 28th day of ATG administration, the body weight of the animals in the ATG + P10% group remained decreased, and the body weight of the animals in the non-ATG control group There was no significant difference between the two (Figure 2).
- the body weight decreased to about the same weight as normal mice immediately after using 10% D-psicose aqueous solution as drinking water.
- the weight loss when D-psicose 10% aqueous solution was used as drinking water remained even after the drinking water was changed to distilled water.
- the body weight was reduced by the D-psicose 10% aqueous solution. The body weight was not significantly lower than that of normal mice.
- D-psicose and / or a derivative thereof has the effect of suppressing weight gain and reducing the weight gain in obese animals. I got it. This is a result of presuming that D-psicose and / or its derivatives show an effect of preventing obesity and / or improving obesity in humans, and provides a new means for preventing and dealing with obesity. is there.
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Abstract
Description
明 細 書 Specification
D—プシコースを含有する体重増加抑制性組成物およびその利用方法 技術分野 D-psicose-containing weight gain inhibitory composition and method of use thereof TECHNICAL FIELD
[0001] 本発明は D—プシコースの有する体重増加抑制および/または過体重減少効果の 利用に関する。より詳細には本発明は、種々の原因による体重の過剰な増加を抑制 し、過体重を減少させることができ、肥満を防止、軽減することが可能で、過剰の体重 増加傾向あるいは過体重にある人および/または動物に適した D—プシコースおよび /またはその誘導体を含有する組成物、食品、食品素材、食品添加物、飲料、飲料 水、薬剤、製剤原料、飼料に関する。また本発明は、種々の原因による体重増加を 抑制および/または過体重を減少させる方法に関する。 [0001] The present invention relates to the use of D-psicose to suppress weight gain and / or to reduce overweight. More specifically, the present invention can suppress excessive weight gain due to various causes, reduce overweight, prevent and reduce obesity, and prevent excessive weight gain or overweight. The present invention relates to a composition, food, food material, food additive, beverage, drinking water, drug, drug substance, and feed containing D-psicose and / or a derivative thereof suitable for a person and / or animal. The present invention also relates to a method for suppressing weight gain and / or reducing overweight due to various causes.
背景技術 Background art
[0002] 希少糖は天然に存在するが、その存在量が極めて微量である単糖を ヽぅ。希少糖 は化学構造により、アルドース、ケトースおよびアルコールに分けられる。アルドース 類としては例えば D—ァロース力 ケトース類としては例えば D—プシコース力 アル コール類としては例えばァリトールがある。しかし、従来これら希少糖の大部分は大量 生産ができず入手困難であったため、その生理活性や薬理活性に関する研究はほ とんどなされていな力つた。最近、香川大学農学部何森教授らにより酵素を用いた大 量生産方法が開発され、 D—プシコース、 D—ァロース、ァリトールなどいくつかの希 少糖が生産されるようになり、その生物活性に関する研究が進んでいる。 [0002] Although rare sugars exist in nature, the abundance is extremely small. Rare sugars are divided into aldoses, ketoses and alcohols by chemical structure. Examples of aldoses include D-alose strength. Examples of ketoses include D-psicose strength. Examples of alcohols include aritol. However, since most of these rare sugars have been difficult to obtain because they were not mass-produced in the past, little research has been conducted on their physiological and pharmacological activities. Recently, a large-scale production method using enzymes was developed by Prof. Irimori et al., Faculty of Agriculture, Kagawa University, and some rare sugars such as D-psicose, D-allose, and aritol were produced. Research is progressing.
[0003] これまでの研究結果から、希少糖には糖代謝あるいは脂質代謝に対する作用をも つ糖が存在することが明らかにされている。例えば、 D—プシコースについては、 in vi tro実験において、摘出腸管での D-Glucose輸送の抑制 (非特許文献 1)、ラット脾 j8 細胞株からのインスリン分泌促進 (特許文献 1)、血管内皮細胞株からの MCP-1分泌 抑制 (特許文献 1)などが、また in vivo実験で、体脂肪蓄積軽減作用 (非特許文献 2)、 生体内ではエネルギーとはならないこと (非特許文献 3)、などが、それぞれ明らかにさ れている。 [0003] From the results of previous studies, it has been clarified that rare sugars have sugars that have an effect on sugar metabolism or lipid metabolism. For example, for D-psicose, in in vitro experiments, suppression of D-Glucose transport in the isolated intestinal tract (Non-patent Document 1), promotion of insulin secretion from rat spleen j8 cell line (Patent Document 1), vascular endothelial cells Suppression of MCP-1 secretion from strains (Patent Document 1), etc., and in vivo experiments, body fat accumulation mitigating action (Non-Patent Document 2), and not becoming energy in vivo (Non-Patent Document 3), etc. However, each has been clarified.
これまでの研究結果から、希少糖には糖代謝ある!、は脂質代謝に対する作用をも つ糖が存在することが明らかにされている。例えば、 D—プシコースについては、 in vi tro実験において、摘出腸管での D-Glucose輸送の抑制 (非特許文献 1)、ラット脾 j8 細胞株からのインスリン分泌促進 (特許文献 1)、血管内皮細胞株からの MCP-1分泌 抑制 (特許文献 1)、脂肪細胞において中性脂肪の蓄積を抑える働き (非特許文献 2、 3)などが、また in vivo実験で、体脂肪蓄積軽減作用 (非特許文献 4)、生体内ではェ ネルギ一とはならな 、こと (非特許文献 5)など力 それぞれ明らかにされて 、る。 Based on the results of previous studies, rare sugars have sugar metabolism! It has been shown that monosaccharides exist. For example, for D-psicose, in in vitro experiments, suppression of D-glucose transport in the isolated intestinal tract (Non-patent Document 1), promotion of insulin secretion from the rat spleen j8 cell line (Patent Document 1), vascular endothelial cells Suppression of MCP-1 secretion from strains (Patent Document 1), action to suppress the accumulation of neutral fat in adipocytes (Non-Patent Documents 2 and 3), etc. Reference 4), and the energy in the living body, which is not unique (Non-Patent Document 5), have been clarified.
[0004] し力し、これまでの研究で明らかにされた作用は、多くは in vitro実験で見られて!/ヽ るものであり、 in vivo実験の結果も正常動物を用いて見られたものである。従って、希 少糖が肥満など糖代謝あるいは脂質代謝に異常を持つ病態動物においてどのよう な効果を現すかは未だ知られて ヽな ヽ。 [0004] However, many of the effects that have been clarified in previous studies have been seen in / out of in vitro experiments, and the results of in vivo experiments were also seen in normal animals. Is. Therefore, it is still known that the effects of rare sugars in pathological animals with abnormalities in sugar metabolism or lipid metabolism such as obesity are known.
[0005] 非特許文献 1 :平成 11年度科学技術総合研究委託費 地域先導研究 研究成果報 告書「希少糖類の医薬品としての作用機序に関する研究」香川医科大学、徳田雅明 、小西良士、前田 肇、平成 12年 [0005] Non-Patent Document 1: Fiscal 1999 Science and Technology Comprehensive Research Commission Regional Lead Research Research Result Report “Study on Mechanisms of Action of Rare Sugars as Pharmaceuticals” Kagawa Medical University, Masaaki Tokuda, Yoshishi Konishi, Maeda Tsuji, 2000
非特許文献 2: 2005年 日本生化学会抄録 (神戸)「脂肪細胞に及ぼす単糖類の影 響」香川大学医学部、斉藤まど香 他 4名。 Non-Patent Document 2: 2005 Japanese Biochemical Society Abstract (Kobe) “Effect of monosaccharides on fat cells” Kagawa University School of Medicine, Madoka Saito and 4 others.
非特許文献 3 : 2006国際生化学会抄録(京都)「Effects of Rare Sugars on the Prope rties of 3T3— LI Adipocytes.」 Non-Patent Document 3: 2006 International Biochemical Society Abstract (Kyoto) “Effects of Rare Sugars on the Properties of 3T3—LI Adipocytes.”
非特許文献 4 :平成 11年度科学技術総合研究委託費 地域先導研究 研究成果報 告書「ラット等を用 ヽた希少糖類の栄養学的評価と食品への応用」香川大学農学部 、鈴木博雄、松尾達博、橋口峰雄、平成 12年 Non-patent document 4: Fiscal 1999 Science and Technology Comprehensive Research Commission Regional Leading Research Research Results Report “Nutritional Evaluation of Rare Sugars Using Rats and Their Application to Food” Kagawa University Faculty of Agriculture, Hiroo Suzuki, Matsuo Tatsuhiro, Hashiguchi Mineo, 2000
非特許文献 5 :平成 12年度科学技術総合研究委託費 地域先導研究 研究成果報 告書「ラット等を用 ヽた希少糖類の栄養学的評価と食品への応用」香川大学農学部 、鈴木博雄、松尾達博、橋口峰雄、平成 13年 Non-Patent Document 5: Fiscal 2000 Science and Technology Research Fund Regional Lead Research Research Results Report “Nutritional Evaluation of Rare Sugars Using Rats and Application to Food” Kagawa University Faculty of Agriculture, Hiroo Suzuki, Matsuo Tatsuhiro, Hashiguchi Mineo, 2001
特許文献 1:国際公開番号 W003/097820 Patent Document 1: International Publication Number W003 / 097820
発明の開示 Disclosure of the invention
発明が解決しょうとする課題 Problems to be solved by the invention
[0006] 現在我が国には肥満とされる人たちが 2300万人いると見られている。これらの人た ちは、単に体重の過剰増加あるいは過体重のみでなぐ高脂血症、高血糖症などを 併発していることが多ぐ生活習慣病の一つとして心臓、血管、脳などに現れるメタボ リックシンドロームなどの疾患による死亡あるいは QOLの低下などの危険にさらされて いる。そのため、体重の過剰な増加を防止し、過体重を減少させる必要性が叫ばれ ている。このためには、医薬品使用より日常的に摂取する食物の質や量の制限と運 動が肥満の治療あるいは予防により有効であると考えられている。しかし、食事制限 や運動は時に行き過ぎとなって、健康そのものを害することもある。 [0006] There are currently 23 million people in the country who are considered obese. These people have hyperlipidemia, hyperglycemia, etc. that are simply overweight or overweight. One of the lifestyle-related diseases that often accompanies is the risk of death from diseases such as metabolic syndrome appearing in the heart, blood vessels, brain, etc., or a decline in QOL. Therefore, there is a need to prevent excessive weight gain and reduce overweight. For this purpose, it is considered that the restriction and movement of the quality and quantity of food taken daily rather than the use of pharmaceuticals are more effective for the treatment or prevention of obesity. However, dietary restrictions and exercise sometimes go too far and can harm health.
[0007] 現在、肥満予防や血中脂質を低減することをうたういわゆる健康食品も多く市販さ れている。これらのいわゆる健康食品は、本来行うべき食事制限や運動の補助として 使う限り有用である。現在、肥満の予防などに用いられているそれらの食品の主成分 には、食物繊維、低カロリー甘味料、アミノ酸混合物などがあるが、いずれも味がよく ない、作用が不確実であるなどの難点がある。そのため、食事制限や運動の補助の ために、作用が確実で使用しゃす 、食品の出現が望まれて!/、る。 [0007] At present, many so-called health foods that promote obesity and reduce blood lipids are also commercially available. These so-called health foods are useful as long as they are used as dietary restrictions and exercise assistance. The main ingredients of those foods currently used for the prevention of obesity include dietary fiber, low-calorie sweeteners, amino acid mixtures, etc., all of which do not taste good and have uncertain effects. There are difficulties. For this reason, the appearance of food is desired for the purpose of restricting meals and assisting exercise, and it is expected to work!
[0008] D—プシコースは蔗糖の約 60%の強さの爽快な甘みを持つ糖で、糖代謝異常は脂 質代謝異常と深い関係にあるため、この希少糖が抗肥満効果を持っている可能性は 大きい。そこで、ヒト肥満のモデル動物を用いて D—プシコースの抗肥満効果につい て検討した。 [0008] D-psicose is a sugar with a refreshing sweetness that is about 60% stronger than sucrose, and abnormal sugar metabolism is closely related to abnormal fat metabolism, so this rare sugar has an anti-obesity effect The potential is great. Therefore, we investigated the anti-obesity effect of D-psicose using human obesity model animals.
[0009] 上記研究の成果に基づく本発明の目的は、体重の過剰増加抑制および過体重減 少が可能で、肥満予防および肥満状態改善を必要とする人および動物に適した D— プシコースおよび/またはその誘導体を含有する組成物、食品、食品素材、食品添加 物、飲料、飲料水、薬剤、製剤原料、飼料などの提供である。また、本発明は、種々 の原因による体重の過剰な増加を抑制し、過体重を減少させる方法の提供を目的と する。 [0009] The purpose of the present invention based on the results of the above studies is to achieve D-psicose and / or suitable for humans and animals that are capable of suppressing overweight and reducing overweight, and that require prevention of obesity and improvement of obesity. Alternatively, the present invention provides a composition, a food, a food material, a food additive, a beverage, drinking water, a drug, a pharmaceutical raw material, a feed and the like containing the derivative. Another object of the present invention is to provide a method for suppressing an excessive increase in body weight due to various causes and reducing an overweight.
課題を解決するための手段 Means for solving the problem
[0010] 上記研究において、肥満モデル動物の体重に対する D—プシコースの効果につい て検討したところ、遺伝的肥満動物の体重増加を抑制し、実験的肥満動物の過体重 を減少させる効果を見いだし、その発見をもとに鋭意研究を重ねて本発明を完成す るに至った。 [0010] In the above study, the effect of D-psicose on the body weight of obese model animals was examined. As a result, the effects of suppressing the body weight gain of genetically obese animals and reducing the overweight of experimental obese animals were found. Based on the findings, the present invention has been completed through extensive research.
[0011] 本発明は、 D—プシコースを含み、体重の過剰増加を抑制することおよび/または 過体重を減少させること、を特徴とする組成物を要旨とする。 [0011] The present invention includes D-psicose, and suppresses excessive weight gain and / or A gist is a composition characterized by reducing overweight.
D—プシコース力^〜 90重量%含まれるように配合されており、本発明は、 D—プシ コースを含み、 D—プシコースカ^〜 90重量%含まれるように配合されている、体重の 過剰増加を抑制することおよび/または過体重を減少させること、を特徴とする組成物 を要旨とする。 D-psicose power is formulated to include ~ 90% by weight, and the present invention includes D-psicose and is formulated to include D-psicoseca ^ -90% by weight. The gist of the present invention is a composition characterized in that it suppresses and / or reduces overweight.
D—プシコースが D—プシコースおよび Zまたはその誘導体であり、本発明は、 D ープシコースおよび Zまたはその誘導体を含み、好ましくは D—プシコースおよび Z またはその誘導体カ^〜 90重量%含まれるように配合されている、体重の過剰増加を 抑制することおよび/または過体重を減少させること、を特徴とする組成物を要旨とす る。 D-psicose is D-psicose and Z or a derivative thereof, and the present invention contains D-psicose and Z or a derivative thereof, preferably formulated so that D-psicose and Z or a derivative thereof is contained in an amount of 90 to 90% by weight. The gist of the present invention is a composition characterized in that it suppresses overweight and / or reduces overweight.
また、本発明は、体重の過剰増加の抑制および/または過体重の減少を必要とする 人および Zまたは動物に対して、上記のいずれかの糸且成物を用いること、を特徴とす る体重の過剰増加を抑制および/または過体重を減少させる方法を要旨とする。 In addition, the present invention is characterized in that any of the above-described yarns and adults is used for a person and Z or an animal who need to suppress overweight and / or reduce overweight. The gist is a method of suppressing overweight and / or reducing overweight.
[0012] 本発明は、 D—プシコースを含み、肥満を予防することおよび Zまたは肥満状態を 改善すること、を特徴とする組成物を要旨とする。 [0012] The gist of the present invention is a composition comprising D-psicose and characterized by preventing obesity and improving Z or obesity status.
D—プシコース力^〜 90重量%含まれるように配合されており、本発明は、 D—プシ コースを含み、 D—プシコースカ^〜 90重量%含まれるように配合されている、肥満を 予防することおよび Zまたは肥満状態を改善すること、を特徴とする糸且成物を要旨と する。 D-psicose strength is formulated to include 90% by weight, and the present invention includes D-psicose, which is formulated to include D-psicose ca ^ -90% by weight, to prevent obesity. And a thread and composition characterized by improving Z and obesity status.
D—プシコースが D—プシコースおよび Zまたはその誘導体であり、本発明は、 D ープシコースおよび Zまたはその誘導体を含み、好ましくは D—プシコースおよび Z またはその誘導体カ^〜 90重量%含まれるように配合されている、肥満を予防するこ とおよび Zまたは肥満状態を改善すること、を特徴とする組成物を要旨とする。 D-psicose is D-psicose and Z or a derivative thereof, and the present invention contains D-psicose and Z or a derivative thereof, preferably formulated so that D-psicose and Z or a derivative thereof is contained in an amount of 90 to 90% by weight. The gist of the present invention is a composition characterized by preventing obesity and improving Z or obesity status.
また、本発明は、肥満の予防および Zまたは肥満状態の改善を必要とする人およ び Zまたは動物に対して、上記のいずれかの組成物を用いること、を特徴とする肥満 を予防およびまたは肥満状態を改善する方法を要旨とする。 The present invention also provides a method for preventing and preventing obesity, characterized by using any of the compositions described above for people and Z or animals that require prevention of obesity and improvement of Z or obesity status. Alternatively, the gist is a method for improving an obesity state.
発明の効果 The invention's effect
[0013] 本発明は、 D—プシコースおよび/またはその誘導体を有効成分とし、体重の過剰 増加抑制および/または過体重減少効果を有する組成物および/または各種の原因 による肥満の予防効果および/または肥満状態の改善効果を有する組成物、ならび にこれらの組成物を用いることを特徴とする、体重の過剰増加を抑制および/または 過体重を減少させる方法および/または各種の原因による肥満を予防および/または 肥満状態を改善させる方法を提供することができる。 [0013] The present invention comprises D-psicose and / or a derivative thereof as an active ingredient, and an excess of body weight. A composition having an inhibitory effect on increase and / or an effect of reducing overweight and / or a composition having an effect of preventing obesity due to various causes and / or an effect of improving obesity, and these compositions are used. It is possible to provide a method for suppressing overweight and / or reducing overweight and / or a method for preventing and / or improving obesity by various causes.
[0014] 本発明は、体重の過剰増加を抑制および/または過体重を減少させることを特徴と し、 D—プシコースおよび/またはその誘導体を有効成分として含有する、食品、保健 用食品、患者用食品、食品素材、保健用食品素材、患者用食品素材、食品添加物 、保健用食品添加物、患者用食品添加物、飲料、保健用飲料、患者用飲料、飲料 水、保健用飲料水、患者用飲料水、薬剤、製剤原料、飼料、患畜および/または患 獣用飼料を提供することができる。 [0014] The present invention is characterized in that it suppresses excess body weight gain and / or reduces overweight, and comprises D-psicose and / or a derivative thereof as an active ingredient, for foods, health foods, and patients. Food, food ingredients, health food ingredients, patient food ingredients, food additives, health food additives, patient food additives, beverages, health drinks, patient drinks, drinking water, health drinks, patients Drinking water, medicines, pharmaceutical ingredients, feed, livestock and / or livestock feed.
[0015] また、本発明は D—プシコースおよび/またはその誘導体を含む組成物を用いる、 体重の過剰増加を抑制および/または過体重を減少させる方法および/または各種 の原因による肥満を予防および/または肥満状態を改善させる方法を提供することが できる。 [0015] In addition, the present invention uses a composition containing D-psicose and / or a derivative thereof to suppress overweight and / or reduce overweight and / or prevent obesity caused by various causes. Alternatively, a method for improving obesity can be provided.
図面の簡単な説明 Brief Description of Drawings
[0016] [図 l]Zucker(fa/fa)ラットの体重に及ぼす D- Psicose反復投与の影響〔図中、 * ;p< 0 . 05, * * ;p< 0. 01 (vs 蒸留水投与群)〕。 [Fig.l] Effect of repeated administration of D-Psicose on body weight of Zucker (fa / fa) rats [In the figure, *; p <0.05, * *; p <0.001 (vs distilled water administration group)〕.
[図 2]Aurothioglucose(ATG)投与マウスの体重におよぼす D- Psicoseの影響〔図中、 * * ;p< 0. 01 (vs ATG対照群)〕。 FIG. 2 shows the effect of D-Psicose on the body weight of mice administered with Aurothioglucose (ATG) [in the figure, * *; p <0.01 (vs ATG control group)].
発明を実施するための最良の形態 BEST MODE FOR CARRYING OUT THE INVENTION
[0017] D—プシコースについては、近年、ェピメラーゼの出現(例えば、特開平 6— 12577 6号公報参照)により、たとえば自然界に豊富に存在する単糖である D—フラクトース より生産できるようになるなど、依然高価ではあるが、比較的入手が容易となった。原 料として D—フラクトースを用いることにより、原料コストの問題を解決し、 D—プシコ一 スに基づく新たな生理活性を有することが期待できるヘテロオリゴ糖が得られることを 見出した。単糖類の中で、 D—プシコースは、還元基としてケトン基を持つ六単糖で ある。この D—プシコースには光学異性体として D体と L体とが有ることが知られている 。ここで、 D—プシコースは既知物質であるが自然界に希にしか存在しないので、国 際希少糖学会の定義によれば「希少糖」と定義されている。 [0017] With regard to D-psicose, in recent years, with the advent of epimerase (see, for example, JP-A-6-125776), for example, it has become possible to produce it from D-fructose, which is a monosaccharide abundant in nature. Although it is still expensive, it has become relatively easy to obtain. It was found that by using D-fructose as a raw material, the problem of raw material cost was solved and a hetero-oligosaccharide expected to have a new physiological activity based on D-psicose was obtained. Among monosaccharides, D-psicose is a hexasaccharide having a ketone group as a reducing group. This D-psicose is known to have D and L isomers as optical isomers. . Here, D-psicose is a known substance but rarely exists in nature, so it is defined as “rare sugar” according to the definition of the International Association of Rare Sugars.
[0018] 希少糖とは自然界に希にしか存在しない単糖 (アルドース、ケトースおよび糖アルコ ール)と定義づけることができる。本発明においても上記の定義に基づく希少糖であ り、好ましくはケトースの D-プシコースである。この定義は糖の構造や性質による定義 ではないため、あいまいである。すなわち、一定量以下の存在量を希少糖というなど の量の定義はなされていないためである。しかし、一般に自然界に多量に存在する アルドースとしては D-グルコース、 D-ガラクトース、 D-マンノース、 D-リボース、 D-キ シロース、 L-ァラビノースの 6種類あり、それ以外のアルドースは希少糖と定義される 。ケトースとしては、 D-フラクトースが存在しており、他のケトースは希少糖といえる。 他のケトースとして、 D-タガトース、 D-ソルボース、 L-フラクトース、 L-プシコース、 L- タガトース、 L-ソルボースが挙げられる。また糖アルコールは単糖を還元してできるが 、 自然界には D—ソルビトールが比較的多いがそれ以外のものは量的には少ないの で、これらも希少糖といえる。 [0018] Rare sugars can be defined as monosaccharides (aldoses, ketoses and sugar alcohols) that rarely exist in nature. Also in the present invention, it is a rare sugar based on the above definition, and preferably ketose D-psicose. This definition is ambiguous because it is not a definition of sugar structure or properties. That is, there is no definition of an amount such as a rare sugar that is less than a certain amount. However, there are six types of aldoses that are generally abundant in nature: D-glucose, D-galactose, D-mannose, D-ribose, D-xylose, and L-arabinose. Other aldoses are defined as rare sugars. Is done. As ketose, D-fructose exists, and other ketoses are rare sugars. Other ketoses include D-tagatose, D-sorbose, L-fructose, L-psicose, L-tagatose, and L-sorbose. Sugar alcohol can be produced by reducing monosaccharides, but D-sorbitol is relatively large in nature, but the others are quantitatively small, so these are also rare sugars.
本発明で用いる希少糖 D—プシコースは、これまで入手自体が困難であった力 自 然界に多量に存在する単糖から希少糖を大量生産する方法が開発されつつあり、そ の技術を利用して製造することができる。 The rare sugar D-psicose used in the present invention has been developed as a method for mass production of rare sugars from monosaccharides existing in large quantities in nature. Can be manufactured.
[0019] 本発明で用いる D-プシコースの誘導体について説明する。ある出発化合物から分 子の構造を化学反応により変換した化合物を出発化合物の誘導体と呼称する。 D-プ シコースを含む六炭糖の誘導体には、糖アルコール (単糖類を還元すると、アルデヒ ド基およびケトン基はアルコール基となり、炭素原子と同数の多価アルコールとなる) や、ゥロン酸(単糖類のアルコール基が酸化したもので、天然では D-グルクロン酸、 ガラクチュロン酸、マンヌロン酸が知られている)、アミノ糖 (糖分子の OH基力NH2基 で置換されたもの、ダルコサミン、コンドロサミン、配糖体などがある)などが一般的で あるが、それらに限定されるものではない。 [0019] The D-psicose derivative used in the present invention will be described. A compound obtained by converting the structure of a molecule from a certain starting compound by a chemical reaction is called a derivative of the starting compound. Derivatives of hexose containing D-psicose include sugar alcohols (when monosaccharides are reduced, aldehyde groups and ketone groups become alcohol groups and polyhydric alcohols of the same number as carbon atoms), uronic acid ( It is an oxidized monosaccharide alcohol group. Naturally, D-glucuronic acid, galacturonic acid, and mannuronic acid are known. Amino sugar (substituted with OH group NH2 group of sugar molecule, darcosamine, chondrosamine) , Glycosides, etc.) are common, but are not limited thereto.
[0020] 希少糖は微量ではあるが天然に存在する単糖である。 D—プシコースについてはヒ トに対する毒性の報告はなぐ動物に対する毒性は低いと考えられる。また、 D—プシ コースは水に溶けやすぐ蔗糖の約 60%の強さの爽快な甘みを持つ糖であり、その 甘味は上品で爽やかで、サッカリンのような苦みや渋みを伴う不快感はなぐむしろフ ラタトースの甘味に類似している。 D—プシコースは、酸味、塩から味、渋味、旨味、 苦味など、各種の物質の他の呈味とよく調和し、普通一般の飲食物の甘味付、呈味 改良に、また品質改良などに有利に利用できる。 [0020] Rare sugars are naturally occurring monosaccharides, albeit in trace amounts. D-psicose is considered to be less toxic to animals, with no reported toxicity to humans. D-psicose is a sugar with a refreshing sweetness that dissolves in water and is about 60% stronger than sucrose. The sweetness is refined and refreshing, and it resembles the sweetness of fratatose rather than the discomfort associated with bitterness and astringency like saccharin. D-psicose is in harmony with other tastes of various substances such as acidity, salt to taste, astringency, umami, bitterness, etc., for sweetening and taste improvement of ordinary foods and beverages, quality improvement, etc. Can be advantageously used.
本発明が対象とする組成物 (食品、保健用食品、患者用食品、食品素材、保健用 食品素材、患者用食品素材、食品添加物、保健用食品添加物、患者用食品添加物 、飲料、保健用飲料、患者用飲料、飲料水、保健用飲料水、患者用飲料水、薬剤、 製剤原料、飼料、患畜および/または患獣用飼料)は、 D—プシコースおよび/または その誘導体を含む食用および/ある 、は薬用の組成物であれば何でもよ ヽ。 Compositions targeted by the present invention (food, health food, patient food, food material, health food material, patient food material, food additive, health food additive, patient food additive, beverage, Health drinks, patient drinks, drinking water, health drinks, patient drinks, medicines, pharmaceutical ingredients, feeds, livestock and / or feeds for patients) are edible containing D-psicose and / or its derivatives And / or is any medicinal composition.
D-プシコースを有効成分とする組成物は、体重の過剰増加を抑制するおよび/また は過体重を減少させるための食品添加物、食品素材、飲食品、医薬品 ·医薬部外品 および飼料力もなる群力も選ばれる形態のものである。その組成物の機能性を生か して健康飲食品、患者用栄養飲食品を謳った食品、同様に、家畜、家禽、魚などの 飼育動物のための飼料の開発が可能となった。 A composition containing D-psicose as an active ingredient also serves as a food additive, food material, food and drink, pharmaceutical / quasi-drug, and feed power to suppress overweight and / or reduce overweight. The group power is also selected. Utilizing the functionality of the composition, it became possible to develop healthy foods and drinks, foods with nutritional foods and drinks for patients, and feed for domestic animals such as livestock, poultry and fish.
すなわち、上記飲食品が、体重の過剰増加を抑制するおよび/または過体重を減 少させるための、機能性食品、栄養補助食品または健康飲食品である。上記飼料が 、体重の過剰増加を抑制するおよび/または過体重を減少させるための、家畜、家禽 、ペット類の飼料である。具体的には、上述した D—プシコースを有効成分とする組 成物の食品素材を、食品形態、飲料形態または飼料形態のいずれの形態で使用す ることがでさる。 That is, the food or drink is a functional food, a nutritional supplement, or a healthy food or drink for suppressing excessive increase in body weight and / or reducing overweight. The above feed is a feed for livestock, poultry and pets for suppressing excess weight gain and / or reducing overweight. Specifically, the food material of the composition containing the above-mentioned D-psicose as an active ingredient can be used in any form of food, beverage or feed.
本発明の D-プシコースを有効成分とする組成物が有する上述した機能性を生かし て用いる場合は、その含量は、特に制限されないが、目的とする機能の度合い、使 用態様、使用量等により適宜調整することができ、例えば 0. 05〜100質量%である 。体重の過剰増加を抑制するおよび/または過体重を減少させるための組成物は、 人体やその他飲食物、医薬品、飼料や皮膚外用剤に使用することができる。また、経 口等により内服することも、皮膚等に塗布することもできる。常法にしたがって経口、 非経口の製品に配合することができ、調味料、食品添加物、食品素材、飲食品、健 康飲食品、皮膚外用剤、医薬品および飼料等の様々な分野で利用することができる 。例えば、飲食物に配合した場合には、体重の過剰増加を抑制するおよび/または 過体重を減少させるべき疾患を治療または予防するための飲食物を提供することが できる。予防等の効果からは、健康食品、栄養食品等として用いられることも期待で きる。その他、家畜、および Zまたは魚類の飼料、餌料に利用することができる。人体 やその他飲食物、医薬品、肥料、飼料や皮膚外用剤に使用することにより、体重の 過剰増加を抑制するおよび/または過体重を減少させるべき疾患を治療または予防 する効果を得ることがでさる。 In the case of using the above-mentioned functionality of the composition containing D-psicose of the present invention as an active ingredient, its content is not particularly limited, but it depends on the degree of intended function, usage mode, usage amount, etc. It can be adjusted as appropriate, for example 0.05 to 100% by mass. The composition for suppressing overweight and / or reducing overweight can be used for the human body, other foods and drinks, pharmaceuticals, feeds, and external preparations for skin. In addition, it can be taken by mouth or applied to the skin. Can be formulated into oral and parenteral products according to conventional methods, and used in various fields such as seasonings, food additives, food ingredients, food and drink, health food and drink, topical skin preparations, pharmaceuticals and feed be able to . For example, when blended in foods and drinks, foods and drinks can be provided for treating or preventing diseases that should suppress excess body weight gain and / or reduce overweight. From the prevention effect, it can be expected to be used as health food, nutritional food, etc. In addition, it can be used for livestock and feed or feed for Z or fish. By using it in the human body, other foods and drinks, pharmaceuticals, fertilizers, feeds, and external preparations for skin, it is possible to obtain an effect of treating or preventing an overweight and / or a disease that should reduce overweight. .
[0022] 本発明の糸且成物においては、 D—プシコースおよび/またはその誘導体は、通常、 組成物中に 0.1〜50重量%含まれるように配合されて 、る。好ましくは 1〜50重量%、 より好ましくは 10〜30重量%である。ただし、含有量が少ない場合には組成物の摂取 量を増やせば良く含有量が多 、場合には組成物の摂取量を少なくすれば良 、。よつ て、配合割合について、通常飲食品には下限に近い配合割合で用いることができる 力 医薬品、錠剤やカプセルに入れて用いるような場合は上限に近い配合割合で用 いることができる。 D—プシコースおよび/またはその誘導体をヒトが摂取する場合、個 々人の年齢、体重および症状などによって用法用量が決定されるべきであるが、多く の場合有効な用量は D—プシコース成人 1日当たり l〜50gで、分割して食前、食後あ るいは食事とともに摂取されるのが適当である。 D—プシコースおよび Zまたはその 誘導体の投与量は、経口投与の場合、成人に対し D—プシコースとして、 1日量 0.3 〜50gを摂取するのが好ましいが、年令、症状により適宜増減することも可能である。 前記 1日量の本発明の肥満予防および Zまたは改善剤は、 1日に 1回、又は適当な 間隔をおいて 1日 2もしくは 3回に分けて、あるいは食前、食後あるいは食事とともに 摂取することが好ましい。 [0022] In the yarn composition of the present invention, D-psicose and / or a derivative thereof is usually blended so as to be contained in an amount of 0.1 to 50% by weight in the composition. Preferably it is 1-50 weight%, More preferably, it is 10-30 weight%. However, if the content is low, it is sufficient to increase the intake of the composition. If the content is high, if the content is low, the intake of the composition may be reduced. Therefore, with regard to the blending ratio, it can be used at a blending ratio close to the lower limit for ordinary foods and beverages. When used in pharmaceuticals, tablets and capsules, it can be used at a blending ratio close to the upper limit. When humans take D-psicose and / or its derivatives, the dosage should be determined by the individual's age, weight and symptoms, etc., but in many cases the effective dose is D-psicose per adult It is appropriate to take 1-50g in divided doses before meals, after meals or with meals. The dose of D-psicose and Z or its derivatives is preferably taken as an oral dose of 0.3 to 50 g daily for adults as D-psicose, but may be increased or decreased appropriately depending on age and symptoms. Is possible. The daily anti-obesity and Z or ameliorating agent of the present invention should be taken once a day, or divided into 2 or 3 times a day at an appropriate interval, or before, after or after meals. Is preferred.
[0023] 本発明の組成物を食品に利用する場合、そのままの形態、オイルなどに希釈した 形態、乳液状形態食、または食品業界で一般的に使用される担体を添加した形態な どのものを調製してもよい。飲料の形態は、非アルコール飲料またはアルコール飲料 である。非アルコール飲料としては、例えば、炭酸系飲料、果汁飲料、ネクター飲料 などの非炭酸系飲料、清涼飲料、スポーツ飲料、茶、コーヒー、ココアなど、また、ァ ルコール飲料の形態では薬用酒などの一般食品の形態を挙げることができる。本発 明の組成物の、前記糖質代謝異常および/または脂質代謝異常改善を目的とした食 品素材あるいは食品添加物としての使用形態としては、錠剤、カプセル剤、飲料など に溶解させる粉末あるいは顆粒などの固形剤、ゼリーなどの半固形体、飲料水など の液体、希釈して用いる高濃度溶液などがある。さらに、本発明の組成物を適宜食 品に添加して肥満予防および Zまたは改善などを目的とした保健食または病人食と することができる。 [0023] When the composition of the present invention is used for foods, it is in a form as it is, a form diluted with oil, a milk form meal, or a form to which a carrier generally used in the food industry is added. It may be prepared. The beverage form is a non-alcoholic beverage or an alcoholic beverage. Non-alcoholic beverages include, for example, non-carbonated beverages such as carbonated beverages, fruit juice beverages, and nectar beverages, soft drinks, sports beverages, tea, coffee, cocoa, etc. The form of food can be mentioned. Main departure Examples of the use of the light composition as a food material or food additive for the purpose of improving the above abnormalities of carbohydrate metabolism and / or lipid metabolism include powders or granules dissolved in tablets, capsules, beverages, etc. Solids, semi-solids such as jelly, liquids such as drinking water, and high-concentration solutions used after dilution. Furthermore, the composition of the present invention can be appropriately added to foods to provide health foods or sick foods for the purpose of obesity prevention and Z or improvement.
任意的成分として、通常食品に添加されるビタミン類、炭水化物、色素、香料など 適宜配合することができる。食品は液状または固形の任意の形態で食することができ る。ゼラチンなどで外包してカプセル化した軟カプセル剤として食することができる。 カプセルは、例えば、原料ゼラチンに水を加えて溶解し、これに可塑剤 (グリセリン、 D —ソルビトールなど)を加えることにより調製したゼラチン皮膜でつくられる。 As optional components, vitamins, carbohydrates, pigments, fragrances and the like that are usually added to foods can be appropriately blended. The food can be eaten in any form, liquid or solid. It can be eaten as a soft capsule encapsulated by gelatin or the like. Capsules are made, for example, with a gelatin film prepared by adding water to raw gelatin and dissolving it, and then adding a plasticizer (such as glycerin or D-sorbitol).
[0024] 本発明の食品素材および食品添加物について説明する。 D—プシコースは水に溶 けやすいため、コーヒーやジュースなどの飲料や菓子類および各種の加工食品に容 易に添加することができる。さら〖こ、本発明の組成物を適宜食品および/または食品 素材に添加して肥満予防および/または肥満状態改善などを目的とした保健用およ び/または患者用加工食品とすることができる。本発明の組成物は、肥満予防および /または肥満状態改善を必要とする人および動物が一般の食事とともに摂食、服用あ るいは飲用する食品を作るための食品素材および/または食品添加物として用いるこ とができ、体重の過剰な増加を予防し、過体重状態を改善して QOLをたかめるととも に、同様の目的で用いられる薬剤あるいは他の食品の効果を補強し、その使用量を 低減することができる。 [0024] The food material and food additive of the present invention will be described. Since D-psicose is soluble in water, it can be easily added to beverages such as coffee and juice, confectionery, and various processed foods. Furthermore, the composition of the present invention can be appropriately added to foods and / or food materials to obtain processed foods for health and / or patients for the purpose of preventing obesity and / or improving obesity. . The composition of the present invention is used as a food material and / or a food additive for preparing food that can be eaten, taken or taken by a person and animals who need obesity prevention and / or improvement of obesity with a general meal. It can be used to prevent excessive weight gain, improve overweight, increase QOL, reinforce the effects of drugs or other foods used for similar purposes, and reduce the amount used. Can be reduced.
[0025] D—プシコースおよび/またはその誘導体をヒトが摂取する場合、個々人の年齢、体 重および症状などによって用法用量が決定されるべきである力 多くの場合有効な 用量は希少糖 1日当たり l〜50gで、分割して食前、食後あるいは食事とともに摂取さ れるのが適当である。 [0025] When D-psicose and / or its derivatives are ingested by humans, the dosage should be determined by the individual's age, weight and symptoms, etc. In many cases, effective doses are rare sugars per day. It is appropriate to take -50g in divided doses before meals, after meals or with meals.
[0026] 本発明の組成物の、前記肥満予防および/または肥満状態改善などを目的とした 食品素材あるいは食品添加物としての使用形態としては、錠剤、カプセル剤、飲料な どに溶解させる粉末あるいは顆粒などの固形剤、ゼリーなどの半固形体、飲料水など の液体、希釈して用いる高濃度溶液などがある。さらに、本発明の組成物を適宜食 品に添加して肥満予防および/または肥満状態改善などを目的とした保健食または 病人食とすることができる。 [0026] The use form of the composition of the present invention as a food material or food additive for the purpose of preventing obesity and / or ameliorating obesity, etc. includes powders dissolved in tablets, capsules, beverages, etc. Solid agents such as granules, semi-solid bodies such as jelly, drinking water, etc. Liquid, high-concentration solution to be used after dilution. Furthermore, the composition of the present invention can be appropriately added to foods to provide health foods or sick foods for the purpose of preventing obesity and / or improving obesity.
[0027] 本発明の飲料水について説明する。肥満は摂取カロリーと消費カロリーのアンバラ ンスカも現われるが、その原因が生活習慣に深く根ざしているため治療は困難である 。現在我が国では食欲減退薬などの肥満治療薬は認められておらず、食事制限な どによる生活習慣の修正と運動が肥満治療の方法として行われている。しかし、食事 制限や運動は肥満状態にある人たちにとっては大きなストレスとなっている。また、過 体重ではないにも拘わらず体重を減らすために食事制限などを行い、栄養バランス が崩れて体調を悪化させると ヽぅ状況も見られて!/ヽる。 [0027] The drinking water of the present invention will be described. Obesity also presents an unbalanced calorie intake and calorie consumption, which is difficult to treat because the cause is deeply rooted in lifestyle. Currently, no anti-obesity drugs such as anorexic drugs have been approved in Japan, and lifestyle modifications and exercises such as dietary restrictions are being carried out as methods for treating obesity. However, dietary restrictions and exercise are a great stress for people who are obese. In addition, even if you are not overweight, you may have dietary restrictions to lose weight, and if you lose your nutritional balance and worsen your physical condition, you will also be in a habit!
[0028] 本発明の飲料水は、 D—プシコースおよび/またはその誘導体を 1〜5重量%含む 無色透明で無臭、ほとんど無味の水溶液である。好ましくは 1.5〜4重量%、より好ま しくは 2〜3重量%である。 1重量%未満であると肥満予防および/または肥満状態改 善効果が十分ではなぐ 5重量%を超えると砂糖の 60%の甘みを有する D—プシコ ース由来の甘みを感ずるようになる。この飲料水は、無色透明でにおいはなぐかす 力な甘みを有している。したがって、そのまま飲料水として飲用できるとともに、炊飯、 調理やお茶、コーヒーなどを淹れるためにも使用できる。本発明の飲料水をこのよう に日常の食事や嗜好品を作るために使用することにより、食事制限を緩和し、特に意 識することなく体重を制御することができる。また、本発明の基礎となった研究結果か ら、正常範囲にある体重には影響を与えないことが推測されるので、より安全に体重 調節を行うことができると考えられる。このことは、過体重や体重の過剰増加に悩む人 たちの QOLの向上に益するものである。 [0028] The drinking water of the present invention is a colorless and transparent, odorless, almost tasteless aqueous solution containing 1 to 5% by weight of D-psicose and / or a derivative thereof. The amount is preferably 1.5 to 4% by weight, more preferably 2 to 3% by weight. If it is less than 1% by weight, the effect of preventing obesity and / or improving the condition of obesity is not sufficient. If it exceeds 5% by weight, the sweetness derived from D-psicose, which has 60% sweetness of sugar, can be felt. This drinking water is colorless and transparent, and has a strong sweetness that smells. Therefore, it can be used as drinking water as it is, and can also be used for cooking rice, cooking, tea and coffee. By using the drinking water of the present invention to make daily meals and luxury goods in this way, dietary restrictions can be relaxed and body weight can be controlled without particular awareness. In addition, it is presumed that the body weight within the normal range is not affected from the research results on which the present invention is based, so that it is considered that the body weight can be adjusted more safely. This will help improve the quality of life for those who are overweight or overweight.
[0029] 本発明の薬剤について説明する。本発明者は、 D—プシコースのラット体重に対す る作用について、遺伝的および実験的肥満モデル動物を用いて詳細に検討した。そ の結果、 D—プシコースには体重増加抑制および過体重減少効果があることを見い だした。 [0029] The agent of the present invention will be described. The present inventor examined in detail the effect of D-psicose on the body weight of rats using genetic and experimental obesity model animals. As a result, we found that D-psicose has the effect of suppressing weight gain and reducing overweight.
[0030] D—プシコースおよび/あるいはその誘導体を有効成分とする、肥満予防および/ま たは肥満状態改善効果を目的とする薬剤は、これらを単独で用いるほか、一般的賦 形剤、安定剤、保存剤、結合剤、崩壊剤などの適当な添加剤を配合し、液剤、顆粒 剤、細粒剤、散剤、錠剤、カプセル剤、丸剤、軟膏剤、貼付剤、散布剤、スプレー剤 または注射剤等の適当な剤型を選んで製剤し、経口的、経鼻的、経皮的あるいは経 静脈的に投与することができる。 [0030] Drugs containing D-psicose and / or its derivatives as an active ingredient for the purpose of preventing obesity and / or improving obesity status are used alone or in general. Formulated with appropriate additives such as form, stabilizer, preservative, binder, disintegrant, liquid, granule, fine granule, powder, tablet, capsule, pill, ointment, patch, spray An appropriate dosage form such as an agent, spray or injection can be selected and formulated and administered orally, nasally, transdermally or intravenously.
[0031] 本発明の組成物を薬剤として臨床に適用するに際しては、有効成分として D—プシ コースおよび/あるいはその誘導体を、固体、半固体または液体の医薬用担体、例え ば希釈剤、賦形剤、安定剤等の添加剤とともに含む製剤とすることが望ましい。前記 有効成分の担体成分に対する割合は、 1〜90重量%の間で変動させ得る。剤型およ び投与形態としては、液剤、顆粒剤、細粒剤、散剤、錠剤、カプセル剤、丸剤、軟膏 剤、貼付剤、散布剤、スプレー剤または注射剤などの剤型にして、又は原末のまま経 口投与してもよい。液剤として使用する場合には、経口投与の他に経鼻的あるいは 経静脈的に投与してもよい。 [0031] When the composition of the present invention is applied clinically as a drug, D-psicose and / or a derivative thereof as an active ingredient is used as a solid, semi-solid or liquid pharmaceutical carrier such as a diluent, an excipient. It is desirable to prepare a preparation containing additives such as an agent and a stabilizer. The ratio of the active ingredient to the carrier component can vary between 1 and 90% by weight. The dosage form and mode of administration are liquids, granules, fine granules, powders, tablets, capsules, pills, ointments, patches, sprays, sprays or injections. Or it may be administered orally with the bulk. When used as a liquid, it may be administered nasally or intravenously in addition to oral administration.
[0032] 経口投与、経鼻投与、経皮投与または経静脈投与に適した医薬用の有機又は無 機の固体、半固体又は液体の担体、溶解剤もしくは希釈剤を、本発明の組成物を薬 剤として調製するために用いることができる。水、ゼラチン、乳糖、デンプン、ステアリ ン酸マグネシウム、タルク、動植物油べンジルアルコール、ガム、ポリアルキレングリコ ール、石油榭脂、ヤシ油、ラノリン、又は医薬に用いられる他のキャリアー (担体)は全 て、本発明の組成物を含む薬剤の担体として用いることができる。また、安定剤、湿 潤剤、乳化剤や、浸透圧調整や配合剤の pH維持のための塩類を補助薬剤として適 宜用 、ることができる。 [0032] A pharmaceutical organic or organic solid, semi-solid or liquid carrier, solubilizer or diluent suitable for oral administration, nasal administration, transdermal administration or intravenous administration is used as a composition of the present invention. It can be used to prepare as a medicine. Water, gelatin, lactose, starch, magnesium stearate, talc, animal and vegetable oil benzyl alcohol, gum, polyalkylene glycol, petroleum oil, coconut oil, lanolin, or other carriers used in medicine All can be used as a carrier for a drug containing the composition of the present invention. In addition, stabilizers, moistening agents, emulsifiers, and salts for adjusting the osmotic pressure and maintaining the pH of the compounding agent can be appropriately used as auxiliary agents.
[0033] さらに、本発明の組成物を含有する薬剤は、肥満予防および/または肥満状態改 善において、本発明の薬剤とともに適切に投与することができる他の医薬として有効 な成分を含有していてもよい。顆粒剤、細粒剤、カプセル剤、散剤、錠剤、軟膏剤、 貼付剤、散布剤またはスプレー剤の場合には、本発明の組成物を 5〜80重量%含有 しているのが好ましぐ液剤または注射剤の場合には、対応する量 (割合)は 1〜80重 量%であるのが好ましい。 [0033] Furthermore, the drug containing the composition of the present invention contains other pharmaceutically effective ingredients that can be appropriately administered together with the drug of the present invention in obesity prevention and / or improvement of obesity status. May be. In the case of granules, fine granules, capsules, powders, tablets, ointments, patches, sprays or sprays, it is preferable to contain 5 to 80% by weight of the composition of the present invention. In the case of solution or injection, the corresponding amount (ratio) is preferably 1 to 80% by weight.
[0034] 臨床投与量は、経口投与の場合、成人に対して D—プシコースおよび/またはその 誘導体として 1日量 l〜50gを内服するのが好ましいが、年齢、症状などにより適宜増 減することも可能である。前記 1日量の本発明の薬剤は、 1日 1回又は適当な間隔を 置いて 1日 2回以上にわけて、あるいは食前、食後あるいは食事とともに投与すること が好ましい。 [0034] When administered orally, the clinical dose is preferably taken as an oral dose of 1 to 50 g daily for adults as D-psicose and / or its derivatives, but may be increased as appropriate depending on age, symptoms, etc. It can also be reduced. The daily dose of the agent of the present invention is preferably administered once a day or divided into two or more times at an appropriate interval, or before, after or with a meal.
[0035] 本発明の製剤原料につ!、て説明する。肥満予防および/または肥満状態改善を期 待する他の薬物を薬剤として製造するときに、 D—プシコースおよび/またはその誘 導体を、製剤原料として、一般的賦形剤、安定剤、保存剤、結合剤、崩壊剤などの目 的で使うこともできる。あるいは、例えば続発性に肥満が現れた場合などには原因疾 患の治療に加えて肥満状態の改善が必要となるが、このような場合の原因疾患治療 剤などの製造に、本発明の組成物を上記のような製剤原料としても用いることができ る。この場合の D—プシコースおよび/またはその誘導体の使用量や他の薬物などと の割合は、これら治療薬の製剤中含有量あるいは性質により適宜調整することができ る。 [0035] The preparation raw material of the present invention will be described. When manufacturing other drugs that are expected to prevent obesity and / or improve obesity as a drug, D-psicose and / or its derivative is used as a drug substance as a general excipient, stabilizer, preservative, It can also be used for purposes such as binders and disintegrants. Alternatively, for example, when obesity appears secondary, it is necessary to improve the obesity state in addition to the treatment of the causative disease. The product can also be used as a raw material for preparation as described above. In this case, the amount of D-psicose and / or its derivative used and the ratio with other drugs can be appropriately adjusted depending on the content or nature of these therapeutic agents in the preparation.
[0036] [作用] [0036] [Action]
遺伝的肥満ラットにおいて D—プシコースの連続経口投与はラットの体重増加を抑 制した。また、実験的肥満ラットに D—プシコースを連続経口投与した場合には、増 加した体重が減少した。 In genetically obese rats, continuous oral administration of D-psicose suppressed rat weight gain. In addition, when D-psicose was orally administered to experimental obese rats, the increased body weight decreased.
[0037] 本発明を実施例および試験例によりさらに詳細に説明するが、本発明はこれらによ つてなんら限定されるものではな!/、。 [0037] The present invention will be described in more detail by way of examples and test examples, but the present invention is not limited by these! /.
実施例 Example
[0038] 実験に用いた餌の種類:日本クレア (株)製のマウス'ラット 'ハムスター用 CE2 [0038] Type of bait used in the experiment: mouse “rat” hamster CE2 manufactured by Claire Japan
餌の投与方法:自由摂取 Feeding method: free intake
摂餌量: D-プシコース水溶液投与群と対照群とで差は認められな力つた。(実験中の 観察からは、動物の行動にも顕著な変化は認められな力つた。 ) Food intake: D-psicose aqueous solution administration group and control group showed no difference. (Observations during the experiment showed no significant changes in animal behavior.)
[0039] [実験方法] [0039] [Method of experiment]
1.遺伝的肥満ラットを用いた実験 1. Experiments using genetically obese rats
10週齢の雄 Zucker(fa/fa)ラット(以下 Zuc(fa)と示す)を用いた。これらの動物を、蒸 留水投与群 (対照群)、 D—プシコース 0.5g/kg投与群 (P0.5)、 D—プシコース lg/kg投 与群 (Pl)、 D—プシコース 2g/kg投与群 (P2)、 D—プシコース 4g/kg投与群 (P4)、の 5群 に分けた。 D—プシコースは蒸留水に溶解し、投与容量は 10mL/kgとした。 Ten-week-old male Zucker (fa / fa) rats (hereinafter referred to as Zuc (fa)) were used. These animals were administered in distilled water (control group), D-psicose 0.5 g / kg (P0.5), D-psicose lg / kg (Pl), D-psicose 2 g / kg. Group (P2), D-psicose 4g / kg group (P4), 5 groups Divided into. D-psicose was dissolved in distilled water and the administration volume was 10 mL / kg.
上記の D—プシコース溶液あるいは蒸留水を 1日 1回強制経口投与した。体重は 3 あるいは 4日間隔で測定した。測定値は平均値および標準誤差で表わし、有意差検 疋 ·ίま Tukey multiple range test 用 ヽて行った。 The above D-psicose solution or distilled water was orally administered by gavage once a day. Body weight was measured at 3 or 4 day intervals. The measured values were expressed as mean values and standard errors, and were performed using a significant difference test or a Tukey multiple range test.
2.実験的肥満マウスを用いた実験 2. Experiments using experimental obese mice
4週齢の ddY系マウスを用いた。実験的に肥満を起こすために、 Aurothioglucose(A TG) 4-week-old ddY mice were used. Aurothioglucose (A TG) for experimental obesity
500mg/kgを腹腔内に投与した。投与 15日目には、 ATGを投与したマウス 60匹のうち 、 7匹が死亡し、 53匹が生存していた。生存マウスのうち、 ATGを投与しな力つた動物 ( 非 ATG対照群)の体重の平均値 +標準偏差 X 2以上の体重を持つ動物を実験的肥 満マウスとした。 53匹の生存マウスのうち、実験的肥満マウスは 26匹であった。 500 mg / kg was administered intraperitoneally. On the 15th day of administration, 7 mice died out of 60 mice administered ATG, and 53 mice survived. Among surviving mice, animals with a body weight greater than the mean value of the animals (non-ATG control group) that had not been administered ATG (non-ATG control group) + standard deviation X2 were regarded as experimentally fertile mice. Of the 53 surviving mice, 26 were experimental obese mice.
実験的肥満マウスを、蒸留水投与群 (ATG対照群)、 D—プシコース 1%水溶液投与 群 (ATG+P1%)および D—プシコース 10%水溶液投与群 (ATG+P10%)の 3群に分けた。 これら D—プシコース水溶液投与群には、 ATG投与 15日目力ら 28日目までは D—プ シコース水溶液を、 18日目の体重測定以後は蒸留水を、それぞれ飲料水として与え た。 Experimental obese mice are divided into 3 groups: distilled water administration group (ATG control group), D-psicose 1% aqueous solution administration group (ATG + P1%) and D-psicose 10% aqueous solution administration group (ATG + P10%). It was. These D-psicose aqueous solution administration groups were given D-psicose aqueous solution from the 15th day to the 28th day of ATG administration and distilled water after the body weight measurement on the 18th day as drinking water.
体重は 3あるいは 4日間隔で測定した。測定値は平均値および標準誤差で表わし、 ¾ ,g、 検定 iiTukey multiple range testを用 ヽ飞 Tつ 7こ。 Body weight was measured at 3 or 4 day intervals. The measured values are expressed as average values and standard errors. ¾, g, Test iiTukey multiple range test is used.
[実験結果] [Experimental result]
1.遺伝的肥満ラットを用いた実験 1. Experiments using genetically obese rats
Zuc(fa)の実験開始時の平均体重は 405.6 ± 3.0g(N= 100)であつた。対照群の Zuc(fa) の体重は 1日当たり 4から 6g増加し、実験開始後 21日目には 504.4±4.1g(N=20)とな つた。 D—プシコース投与群の動物の体重増加は対照群と較べて少なぐ P4群の体 重は D—プシコース投与 10日目以降の全ての測定時点で対照群と較べて有意差が 見られた。 P2群では、 D—プシコース投与 21日目に対照群と較べて有意に少ない体 重を示した (図 1)。 The average body weight of Zuc (fa) at the start of the experiment was 405.6 ± 3.0 g (N = 100). The body weight of Zuc (fa) in the control group increased from 4 to 6 g per day, and reached 504.4 ± 4.1 g (N = 20) on the 21st day after the start of the experiment. The weight gain of animals in the D-psicose administration group was less than that in the control group. The body weight in the P4 group was significantly different from the control group at all measurement points after the 10th day of D-psicose administration. The P2 group showed significantly less body weight than the control group on day 21 after D-psicose administration (Fig. 1).
2.実験的肥満マウスを用いた実験 2. Experiments using experimental obese mice
ATG投与後 15日目の非 ATG対照群の動物の平均体重は、 36.0±0.8g(N=10)gであ つた。一方、実験的肥満マウスの平均体重は、 39.2 ±0.3g(N=5)gであった。 The average body weight of animals in the non-ATG control group on the 15th day after ATG administration is 36.0 ± 0.8 g (N = 10) g. I got it. On the other hand, the average body weight of experimental obese mice was 39.2 ± 0.3 g (N = 5) g.
実験的肥満マウスで D—プシコースを投与しな力つた場合 (ATG対照群)には体重 は増加し続け、 ATG投与後 42日目には 53.3±3.7g(N=5)gとなった。 D—プシコース 投与群のうち、 ATG+P1%群の動物の体重は、 ATG対照群とほぼ同様に増加し、 ATG 投与 42日目には 55.6±3.5g(N=5)gとなった。 ATG対照群および ATG+P1%群の動物 の体重は、全ての測定時点で非 ATG対照群の動物の体重と較べて有意に大きかつ た。 ATG+P10%群の動物の体重は D—プシコース投与直後に減少し、 D—プシコース 投与期間中 (ATG投与 15日目から 28日目まで)、非 ATG対照群の動物の体重との間 には有意差は見られなかった。 ATG投与 28日目に飲料水を D—プシコース 10%水 溶液から蒸留水に変えた後も、 ATG+P10%群の動物の体重は減少したままで、非 AT G対照群の動物の体重との間には有意差は見られなかった (図 2)。 In experimental obese mice, when D-psicose was administered with little strength (ATG control group), the body weight continued to increase, and on day 42 after ATG administration, it became 53.3 ± 3.7 g (N = 5) g. In the D-psicose group, the body weight of the animals in the ATG + P1% group increased almost the same as in the ATG control group, reaching 55.6 ± 3.5 g (N = 5) g on the 42nd day after ATG administration. The body weight of animals in the ATG control group and ATG + P1% group was significantly greater than the body weight of animals in the non-ATG control group at all time points. The body weight of the animals in the ATG + P10% group decreased immediately after administration of D-psicose, and during the period of administration of D-psicose (from day 15 to day 28 of ATG administration), the body weight of the animals in the non-ATG control group There was no significant difference. Even after changing the drinking water from D-psicose 10% aqueous solution to distilled water on the 28th day of ATG administration, the body weight of the animals in the ATG + P10% group remained decreased, and the body weight of the animals in the non-ATG control group There was no significant difference between the two (Figure 2).
[0041] [考察] [0041] [Discussion]
遺伝的肥満ラットを用いた実験においては、 0.5g/kg以上の D—プシコースを強制 経口投与した場合に、対照群と較べて体重増加が小さい傾向が見られ、 4g/kgを投 与した群では対照群との間に有意な差が見られた。 D—プシコース 4g/kgを投与した 群では、投与開始後 10日目力もその差が明らかとなった。 In experiments using genetically obese rats, when gavage administration of D-psicose of 0.5 g / kg or more tended to show a smaller weight gain compared to the control group, the group receiving 4 g / kg There was a significant difference from the control group. In the group administered D-psicose 4g / kg, the difference was also evident on the 10th day after starting administration.
一方、実験的肥満マウスを用いた実験では、 D—プシコース 10%水溶液を飲料水 とした直後に、正常マウスとほぼ同じ体重にまで減少した。 D—プシコース 10%水溶 液を飲料水としたときに減少した体重は、飲料水を蒸留水に変更した後も持続してい た。また、 D—プシコース 10%水溶液により体重は減少した力 正常マウスの体重より 有意に低くなることはなかった。 On the other hand, in an experiment using experimental obese mice, the body weight decreased to about the same weight as normal mice immediately after using 10% D-psicose aqueous solution as drinking water. The weight loss when D-psicose 10% aqueous solution was used as drinking water remained even after the drinking water was changed to distilled water. Moreover, the body weight was reduced by the D-psicose 10% aqueous solution. The body weight was not significantly lower than that of normal mice.
本研究で、 D—プシコースが病態動物の体重増加を抑制し、増加した体重を減少 させる効果が明らかになつたことは、ヒトにおける糖代謝あるいは脂質代謝の異常に より発現する肥満に対して希少糖が改善効果を現す可能性が大きいことを示すもの である。 In this study, the effect of D-psicose on the suppression of body weight gain in diseased animals and the decrease in increased body weight was found to be rare for obesity caused by abnormal sugar metabolism or lipid metabolism in humans. This indicates that there is a high possibility that sugar will show an improvement effect.
産業上の利用可能性 Industrial applicability
[0042] 本発明により、 D—プシコースおよび/またはその誘導体は肥満病態動物において 体重増加を抑制し、増加した体重を減少させる効果を現すことがはじめて明らかにな つた。このことは、ヒトにおいても D—プシコースおよび/またはその誘導体が肥満予 防および/または肥満状態改善効果を現すことを推測させる結果であり、肥満の予防 ならびに対処に新 、手段を提供するものである。 [0042] According to the present invention, it is clear for the first time that D-psicose and / or a derivative thereof has the effect of suppressing weight gain and reducing the weight gain in obese animals. I got it. This is a result of presuming that D-psicose and / or its derivatives show an effect of preventing obesity and / or improving obesity in humans, and provides a new means for preventing and dealing with obesity. is there.
Claims
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| JP2005-209654 | 2005-07-20 | ||
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| JP2006196753A JP5645183B2 (en) | 2005-07-20 | 2006-07-19 | Obesity improving agent containing D-psicose as an active ingredient |
| JP2006-196753 | 2006-07-19 |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008059625A1 (en) * | 2006-11-17 | 2008-05-22 | National University Corporation Kagawa University | Utilization of the function of rare sugar as promoter for the migration of glucokinase from nucleus to cytoplasm |
| US9259022B2 (en) | 2013-03-15 | 2016-02-16 | Tate & Lyle Ingredients Americas Llc | Sweetener |
| US9491960B2 (en) | 2013-03-15 | 2016-11-15 | Tate & Lyle Ingredients Americas Llc | Sweetener |
| US9854827B2 (en) | 2013-03-15 | 2018-01-02 | Tate & Lyle Ingredients Americas Llc | Sweetener |
| EP3345608B1 (en) * | 2015-09-01 | 2024-11-27 | Cj Cheiljedang Corporation | Method for inhibiting absorption of and promoting excretion of lipids using d-psicose |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007100102A1 (en) * | 2006-03-03 | 2007-09-07 | National University Corporation Kagawa University | Nematicidal composition and nematode eradication method using the same |
| KR20100018568A (en) | 2007-05-18 | 2010-02-17 | 마쓰다니가가꾸고오교가부시끼가이샤 | Novel sweetener having sugar-like taste and production method and use of the same |
| JP6013712B2 (en) | 2011-09-06 | 2016-10-25 | 合同会社希少糖食品 | Biometabolic parameter improving agent comprising D-psicose as an active ingredient |
| JP6581902B2 (en) * | 2013-04-26 | 2019-09-25 | 松谷化学工業株式会社 | Therapeutic and / or preventive agent or method for promoting energy consumption and / or reducing energy consumption function |
| JP6253451B2 (en) * | 2014-02-05 | 2017-12-27 | 学校法人自治医科大学 | Sustained satiety agent and method for maintaining satisfaction |
| JP6948670B2 (en) * | 2017-06-29 | 2021-10-13 | 松谷化学工業株式会社 | Composition for improving biological function containing D-psicose and soy protein as active ingredients |
| CN113453755A (en) * | 2019-02-19 | 2021-09-28 | 国立大学法人香川大学 | Oral composition using Japanese rat thorn containing in vivo functional component in form of plant |
| KR20240108016A (en) * | 2022-12-30 | 2024-07-09 | 주식회사 삼양사 | Improvement of intestinal disease using allulose |
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| JP2005213227A (en) * | 2004-01-30 | 2005-08-11 | Teikoku Seiyaku Co Ltd | Use of blood sugar increase suppressing effect of d-psicose |
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| JP2005213227A (en) * | 2004-01-30 | 2005-08-11 | Teikoku Seiyaku Co Ltd | Use of blood sugar increase suppressing effect of d-psicose |
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| DATABASE BIOSIS [online] MATSUO T. ET AL.: "Effects of dietary D-psicose on diurnal variation in plasma glucose and insulin concentrations of rats", accession no. STN Database accession no. (PREV200600345273) * |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008059625A1 (en) * | 2006-11-17 | 2008-05-22 | National University Corporation Kagawa University | Utilization of the function of rare sugar as promoter for the migration of glucokinase from nucleus to cytoplasm |
| US9259022B2 (en) | 2013-03-15 | 2016-02-16 | Tate & Lyle Ingredients Americas Llc | Sweetener |
| US9491960B2 (en) | 2013-03-15 | 2016-11-15 | Tate & Lyle Ingredients Americas Llc | Sweetener |
| US9635879B2 (en) | 2013-03-15 | 2017-05-02 | Tate & Lyle Ingredients Americas Llc | Sweetener |
| US9854827B2 (en) | 2013-03-15 | 2018-01-02 | Tate & Lyle Ingredients Americas Llc | Sweetener |
| EP3345608B1 (en) * | 2015-09-01 | 2024-11-27 | Cj Cheiljedang Corporation | Method for inhibiting absorption of and promoting excretion of lipids using d-psicose |
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| JP2007051137A (en) | 2007-03-01 |
| JP5645183B2 (en) | 2014-12-24 |
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