WO2011132692A1 - 内臓脂肪蓄積抑制剤 - Google Patents
内臓脂肪蓄積抑制剤 Download PDFInfo
- Publication number
- WO2011132692A1 WO2011132692A1 PCT/JP2011/059681 JP2011059681W WO2011132692A1 WO 2011132692 A1 WO2011132692 A1 WO 2011132692A1 JP 2011059681 W JP2011059681 W JP 2011059681W WO 2011132692 A1 WO2011132692 A1 WO 2011132692A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- visceral fat
- lactic acid
- egg white
- fat accumulation
- liver
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- 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
- A61K35/56—Materials from animals other than mammals
- A61K35/57—Birds; Materials from birds, e.g. eggs, feathers, egg white, egg yolk or endothelium corneum gigeriae galli
-
- 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
- A23L15/00—Egg products; Preparation or treatment thereof
- A23L15/25—Addition or treatment with microorganisms or enzymes
-
- 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
- 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
- A23L33/17—Amino acids, peptides or proteins
-
- 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
-
- 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
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/11—Lactobacillus
Definitions
- the present invention relates to a visceral fat accumulation inhibitor comprising lactic acid fermented egg white as an active ingredient.
- visceral fat mass and liver triglyceride concentration are affected by lifestyle, multiple lipid metabolism systems and constitutional factors are involved, so visceral fat mass and liver triglyceride concentration are not correlated with each other. In many cases, simply improving lifestyle does not control these. Moreover, even if the amount of visceral fat is decreased, there are many cases where the decrease in the triglyceride concentration in the liver is not observed. Although there are methods for controlling these using pharmaceuticals, they may cause side effects and are limited to use under the supervision of a doctor, so they are not suitable for the purpose of improving a condition that has not reached the therapeutic range.
- Patent Document 1 As an invention for improving obesity using food materials, there is a diet food (Patent Document 1) containing milk protein, etc., but the above invention is eaten using a low calorie, high protein, high nutrition and nutritionally balanced food. It aimed at weight loss by improving life, and did not suppress the accumulation of visceral fat or the increase in triglycerides in the liver.
- Patent Document 2 As an invention for reducing lipids using lactic acid fermented egg white, there is a serum cholesterol lowering material (Patent Document 2). However, the invention described above lowers serum cholesterol and suppresses the accumulation of visceral fat, The effect on suppression of triglyceride elevation was not clear.
- this invention aims at providing the visceral fat accumulation
- the inventor unexpectedly significantly suppressed the accumulation of visceral fat and increased triglycerides in the liver. Has been found to significantly suppress the occurrence of the present invention, and the present invention has been completed.
- the visceral fat accumulation inhibitor according to one embodiment of the present invention contains lactic acid fermented egg white as an active ingredient. Moreover, the said visceral fat accumulation inhibitor can have a liver triglyceride rise inhibitory effect. Furthermore, the present invention includes a liver triglyceride elevation inhibitor containing lactic acid fermented egg white as an active ingredient.
- visceral fat accumulation inhibitor or the hepatic triglyceride elevation inhibitor of the present invention it is possible to produce foods and pharmaceuticals that can be safely and comfortably taken and can be expected to prevent hypertension, diabetes, fatty liver and the like.
- the visceral fat accumulation inhibitor of the present invention contains lactic acid fermented egg white as an active ingredient, and has an action of reducing the amount of visceral fat.
- the visceral fat means fat accumulated around the viscera inside the abdominal muscles.
- the visceral fat accumulation inhibitor of the present invention can have an effect of suppressing the increase in triglyceride in the liver, and the present invention includes a liver triglyceride increase inhibitor containing lactic acid fermented egg white as an active ingredient.
- the lactic acid fermented egg white which is an active ingredient of the visceral fat accumulation inhibitor and the liver triglyceride elevation inhibitor of the present invention is obtained by adding lactic acid bacteria to a liquid egg white and fermenting it.
- lactic acid bacteria assimilating saccharides are generally added as a nutrient source, and if necessary, fermentation promoting substances such as yeast extract, and edible fats and oils for the purpose of imparting a rich taste of lactic acid fermented egg white are added.
- the lactic acid bacteria are fermented preferably at 10 3 to 10 8 , more preferably 10 5 to 10 7 per mL, and the present invention may be obtained by the same method.
- egg white used for lactic acid fermented egg white are those obtained by splitting egg yolk from birds such as chickens and industrially obtained, sterilized, frozen, concentrated or diluted, Examples include desugared ones, dried ones rehydrated, and the like. Further, it may contain egg yolk and other egg-derived components to the extent that they do not affect the effect.
- Lactic acid bacteria used in lactic acid fermented egg white are generally used for the production of yogurt and cheese, for example, Lactobacillus genus (Lactobacillus bulgaricus, etc.), Streptococcus genus (Streptococcus thermophilus, Streptococcus diacetosis cactus, Lactococcus, etc. Etc.), Leuconostoc cremoris, etc., Enterococcus faecalis, Bifidobacterium Bifidum, etc.
- Examples of lactic acid bacteria assimilating saccharides used in lactic acid fermented egg white include monosaccharides (glucose, galactose, fructose, mannose, N-acetylglucosamine, etc.), disaccharides (lactose, maltose, sucrose, cerbiose, trehalose, etc.), oligosaccharides (Especially those having 3 to 5 monosaccharides bound thereto), glucose fructose liquid sugar and the like, and one kind or a combination of two or more kinds can be added to the liquid egg white.
- monosaccharides glucose, galactose, fructose, mannose, N-acetylglucosamine, etc.
- disaccharides lactose, maltose, sucrose, cerbiose, trehalose, etc.
- oligosaccharides Especially those having 3 to 5 monosaccharides bound thereto
- the fermentation promoting substance used for lactic acid fermented egg white is not particularly limited as long as it promotes fermentation within a range not impairing the effects of the present invention.
- protein degradation products such as amino acids and peptides, yeast extracts, vitamins, minerals and the like can be mentioned.
- the form of lactic acid fermented egg white can have various forms (for example, liquid, powder, microcolloid, cream, paste, jelly).
- the drying treatment can be carried out by adding a shaping material such as dextrin or an aqueous medium such as fresh water to the lactic acid fermented egg white as necessary, followed by any method such as spray drying, freeze drying, pan drying and the like.
- the typical manufacturing method of lactic acid fermentation egg white is shown below.
- Add 2-8% egg white protein, 1-15% lactic acid bacteria assimilating saccharides, and 0.5-10% fermentation-promoting substance to water, and adjust pH to 5-7.5 using acid materials such as lactic acid and hydrochloric acid.
- acid material it is preferable to use lactic acid from the surface of flavor.
- the obtained preparation liquid is heated at 60 to 110 ° C. for 5 to 120 minutes, and then a lactic acid bacteria starter is added so as to be 10 5 to 10 7 per mL. Fermented at 25-50 ° C. for 8-48 hours to obtain lactic acid fermented egg white.
- the lactic acid fermented egg white may be sterilized by heating and homogenized under high pressure, or may be powdered by drying such as freeze drying or spray drying.
- the visceral fat accumulation inhibitor or the hepatic triglyceride elevation inhibitor of the present invention may be used as one of ingredients such as foods, pharmaceuticals and feeds, or may be used as foods, pharmaceuticals and feeds as they are. .
- the dry weight is 0.1 g or more (hereinafter referred to as 0.1 g / kg ⁇ day) as lactic acid fermented egg white per kg body weight per day. )
- 0.1 g / kg ⁇ day lactic acid fermented egg white per kg body weight per day.
- Lactic acid fermented egg white is a highly safe substance, so that the intake is not particularly limited, but even if it is ingested in excess of 2 g / kg ⁇ day, it is difficult to expect an effect according to the intake and it is not efficient. Therefore, in order for the present invention to fully exert its effect, it is preferable to ingest 0.1 g / kg ⁇ day to 2 g / kg ⁇ day as lactic acid fermented egg white.
- visceral fat accumulation inhibitor or liver triglyceride elevation inhibitor of the present invention will be described in detail below based on Examples and Test Examples. Note that the present invention is not limited to this.
- Example 1 An egg white aqueous solution comprising 34% liquid egg white (protein content 4%), 5% sucrose, 0.05% yeast extract, 0.15% 50% lactic acid and 61.8% fresh water was stirred and prepared. The obtained egg white aqueous solution was heated at 70 to 90 ° C. for 5 minutes, and then added with 0.02% lactic acid bacteria starter (Lactococcus lactis subsp. Lactis, Leuconostoc mesenteroides subsp. After fermentation at 24 ° C. for 24 hours, the mixture was sterilized by heating at 70 to 90 ° C.
- lactic acid bacteria starter Lactis subsp. Lactis, Leuconostoc mesenteroides subsp.
- lactic acid fermented egg white was freeze-dried and ground to obtain a lactic acid fermented egg white powder (protein content 40%) used in the present invention.
- Lactic acid fermented egg white powder (protein content 40%) 43.2 g and methionine 0.3 g, corn starch 15.0 g, sucrose 21.8 g, cellulose 5.0 g, corn oil 10.0 g, mineral mixture 3.5 g (Oriental Yeast Industry Co., Ltd., trade name “AIN-76 Mineral Mix”), Vitamin Mixture 1.0g (Oriental Yeast Industry Co., Ltd., trade name “AIN-76 Vitamin Mix”), 0.2 g choline bitartrate are mixed.
- the feed was prepared. The obtained feed was used in later-described test examples as the visceral fat accumulation inhibitor or the hepatic triglyceride elevation inhibitor of the product of the present invention.
- Example 1 In Example 1, 43.2 g of lactic acid fermented egg white powder (protein content 40%) was added to 20.0 g of dried egg white (86% protein content, product name “Drying Egg White K Type” manufactured by QP Corporation), and sucrose 21. A feed was prepared in the same manner as in Example 1 except that 8 g was changed to 45.0 g.
- Example 2 In Example 1, 43.2 g of lactic acid fermented egg white powder (protein content 40%) was 20.0 g of casein (protein content 86%, manufactured by Oriental Yeast Co., Ltd., trade name “casein”), and 21.8 g of sucrose 45 A feed was prepared in the same manner as in Example 1 except that the amount was changed to 0.0 g.
- the acclimated rats were divided into 3 groups ((A) Example 1 group, (B) Comparative example 1 group, (C) Comparative example 2 group) (8 animals / group)) so that the average body weight was equal, Each group was bred for 4 weeks with each feed. During the breeding period, water was freely consumed, but the daily food intake of the feed was measured and the food intake of all groups was adjusted (pair feeding).
- mice were sacrificed under anesthesia with pentobarbital sodium and dissected to remove visceral fat (mesentery, peri-renal, peri-testis) and liver, and the weight of each individual was measured.
- the visceral fat rate which is an index of visceral fat accumulation, was calculated from the amount of adipose tissue in the mesentery, around the kidney, and around the testis where the tendency of visceral fat accumulation was marked. Specifically, the total value of the above-mentioned adipose tissue per 100 g of final body weight was taken as the visceral fat percentage, and the average values for each group are shown in Table 1.
- the visceral fat rate was significantly reduced by the administration of the visceral fat accumulation inhibitor of the present invention.
- Test Example 2 Liver triglyceride elevation inhibitory effect in rats
- the amount of triglyceride in the liver was measured using the excised liver. Specifically, the liver is homogenized for each individual and extracted with chloroform-methanol by the Folch method to obtain lipids, which are used to measure by the chemical method (Clin. Chim. Acta, 22, 393-397 (1968)). did.
- the concentration of triglyceride in the liver which is an index of the increase in triglyceride in the liver, was calculated as the amount of triglyceride per 1 g of liver (mg), and the average value of each group is shown in Table 2.
- the liver triglyceride concentration was significantly reduced by the administration of the liver triglyceride elevation inhibitor of the present invention.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Obesity (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Mycology (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Microbiology (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
Description
また、上記内臓脂肪蓄積抑制剤は、肝臓中トリグリセリド上昇抑制効果を有することができる。
さらに、本発明は、乳酸発酵卵白を有効成分として含有する肝臓中トリグリセリド上昇抑制剤を包含する。
また、本発明の内臓脂肪蓄積抑制剤は、肝臓中のトリグリセリド上昇を抑制する効果を有することができ、本発明は、乳酸発酵卵白を有効成分として含有する肝臓中トリグリセリド上昇抑制剤を包含する。
液卵白34%(蛋白質含有量4%)、スクロース5%、酵母エキス0.05%、50%乳酸0.15%及び清水61.8%からなる卵白水溶液を攪拌、調製した。得られた卵白水溶液を70~90℃で5分間加熱した後、乳酸菌スターター0.02%(Lactococcus lactis subsp. lactis、Leuconostoc mesenteroides subsp.cremoris、Streptococcus diacetylactis、Lactococcus lactis subsp.cremoris)を添加し、30℃で24時間発酵を行った後、70~90℃で10分間加熱殺菌し、次いで高圧ホモゲナイザーを用いて10MPaの圧力で処理し、本発明の有効成分である乳酸発酵卵白を得た。得られた乳酸発酵卵白を凍結乾燥及び粉砕して本発明に用いる乳酸発酵卵白粉末(蛋白質含量40%)を得た。
実施例1において、乳酸発酵卵白粉末(蛋白質含量40%)43.2gを乾燥卵白(蛋白質含量86%、キユーピータマゴ株式会社製、商品名「乾燥卵白Kタイプ」)20.0gに、スクロース21.8gを45.0gに変更した以外は、実施例1と同様にして飼料を調製した。
実施例1において、乳酸発酵卵白粉末(蛋白質含量40%)43.2gをカゼイン(蛋白質含量86%、オリエンタル酵母工業株式会社製、商品名「カゼイン」)20.0gに、スクロース21.8gを45.0gに変更した以外は、実施例1と同様にして飼料を調製した。
SD系ラット(4週齢)雄を「AIN-76」(米国国立栄養研究所から発表された標準精製飼料)で1週間馴化した(馴化終了時平均体重:104.2g)。
試験例1において、摘出した肝臓を用いて肝臓中のトリグリセリド量を測定した。具体的には、個体毎に肝臓をホモジナイズし、Folch法によりクロロホルム-メタノール抽出して脂質を得、これを用いて化学法(Clin.Chim.Acta,22,393-397(1968))により測定した。
Claims (2)
- 乳酸発酵卵白を有効成分として含有することを特徴とする内臓脂肪蓄積抑制剤。
- 乳酸発酵卵白を有効成分として含有し、肝臓中トリグリセリド上昇抑制効果を有することを特徴とする請求項1記載の内臓脂肪蓄積抑制剤。
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201180019330XA CN102844040A (zh) | 2010-04-22 | 2011-04-20 | 内脏脂肪蓄积抑制剂 |
| JP2012511678A JPWO2011132692A1 (ja) | 2010-04-22 | 2011-04-20 | 内臓脂肪蓄積抑制剤 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010-098577 | 2010-04-22 | ||
| JP2010098577 | 2010-04-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2011132692A1 true WO2011132692A1 (ja) | 2011-10-27 |
Family
ID=44834209
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2011/059681 Ceased WO2011132692A1 (ja) | 2010-04-22 | 2011-04-20 | 内臓脂肪蓄積抑制剤 |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPWO2011132692A1 (ja) |
| CN (1) | CN102844040A (ja) |
| WO (1) | WO2011132692A1 (ja) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006093013A1 (ja) * | 2005-02-28 | 2006-09-08 | Q.P. Corporation | 血清コレステロール低下材およびその製造方法、ならびに血清コレステロール低下作用を有する食品組成物および医薬組成物 |
| JP2006273744A (ja) * | 2005-03-29 | 2006-10-12 | Q P Corp | 血圧降下材およびその製造方法、ならびに血圧降下作用を有する食品組成物および医薬組成物 |
| EP2062587A1 (en) * | 2006-09-04 | 2009-05-27 | Snow Brand Milk Products, Co., Ltd. | Agent for accelerating the increase in and/or preventing the decrease in blood adiponectin level, and visceral fat accumulation inhibitor |
| EP2127660A1 (en) * | 2007-03-02 | 2009-12-02 | Snow Brand Milk Products, Co., Ltd. | Agent for reducing visceral fat |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5089942B2 (ja) * | 2006-09-04 | 2012-12-05 | 雪印メグミルク株式会社 | 内臓脂肪蓄積抑制剤 |
-
2011
- 2011-04-20 WO PCT/JP2011/059681 patent/WO2011132692A1/ja not_active Ceased
- 2011-04-20 CN CN201180019330XA patent/CN102844040A/zh active Pending
- 2011-04-20 JP JP2012511678A patent/JPWO2011132692A1/ja active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006093013A1 (ja) * | 2005-02-28 | 2006-09-08 | Q.P. Corporation | 血清コレステロール低下材およびその製造方法、ならびに血清コレステロール低下作用を有する食品組成物および医薬組成物 |
| JP2006273744A (ja) * | 2005-03-29 | 2006-10-12 | Q P Corp | 血圧降下材およびその製造方法、ならびに血圧降下作用を有する食品組成物および医薬組成物 |
| EP2062587A1 (en) * | 2006-09-04 | 2009-05-27 | Snow Brand Milk Products, Co., Ltd. | Agent for accelerating the increase in and/or preventing the decrease in blood adiponectin level, and visceral fat accumulation inhibitor |
| EP2127660A1 (en) * | 2007-03-02 | 2009-12-02 | Snow Brand Milk Products, Co., Ltd. | Agent for reducing visceral fat |
Non-Patent Citations (3)
| Title |
|---|
| MAKOTO SHIMOYAMADA ET AL.: "Kannetsu Kanso Ranpaku no Shishitsu Taisha Kaizen Sayo", THE 45TH PROCEEDINGS OF JAPANESE SOCIETY OF FOOD SCIENCE AND TECHNOLOGY, 1998, pages 562 * |
| MITSURU FUKUDA ET AL.: "Effects of Lactic Fermentation Processing of Soymilk and Okara on Lipid Metabolism in Rats", THE BULLETIN OF MUKOGAWA WOMEN'S UNIVERSITY (NATURAL SCIENCE), vol. 57, 2009, pages 47 - 54 * |
| YUKA ANDO ET AL.: "Ranpaku Peptide no Rat Shishitsu Taisha ni Oyobosu Eikyo", 62ND THE JAPANESE SOCIETY OF NUTRITION AND FOOD SCIENCE TAIKAI KOEN YOSHISHU, 2008, pages 236 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102844040A (zh) | 2012-12-26 |
| JPWO2011132692A1 (ja) | 2013-07-18 |
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