WO2007043933A1 - Probiotics to influence fat metabolism and obesity - Google Patents

Probiotics to influence fat metabolism and obesity Download PDF

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Publication number
WO2007043933A1
WO2007043933A1 PCT/SE2006/001117 SE2006001117W WO2007043933A1 WO 2007043933 A1 WO2007043933 A1 WO 2007043933A1 SE 2006001117 W SE2006001117 W SE 2006001117W WO 2007043933 A1 WO2007043933 A1 WO 2007043933A1
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WO
WIPO (PCT)
Prior art keywords
product
obesity
probiotics
mice
probiotic
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Ceased
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PCT/SE2006/001117
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English (en)
French (fr)
Inventor
Kajsa Ohlson
Margit Mahlapuu
Ulla Svensson
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Arla Foods AMBA
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Arla Foods AMBA
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Priority to DK06799717.1T priority Critical patent/DK1945235T3/da
Priority to BRPI0616993-7A priority patent/BRPI0616993A2/pt
Priority to ES06799717T priority patent/ES2396865T3/es
Priority to JP2008534487A priority patent/JP2009511469A/ja
Priority to EP06799717A priority patent/EP1945235B1/en
Priority to CA002624890A priority patent/CA2624890A1/en
Priority to AU2006299956A priority patent/AU2006299956B2/en
Priority to EA200800913A priority patent/EA015461B1/ru
Priority to SI200631495T priority patent/SI1945235T1/sl
Application filed by Arla Foods AMBA filed Critical Arla Foods AMBA
Priority to US12/089,433 priority patent/US20080267933A1/en
Priority to CN2006800368040A priority patent/CN101287478B/zh
Priority to PL06799717T priority patent/PL1945235T3/pl
Publication of WO2007043933A1 publication Critical patent/WO2007043933A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66Microorganisms or materials therefrom
    • A61K35/74Bacteria
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/135Bacteria or derivatives thereof, e.g. probiotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66Microorganisms or materials therefrom
    • A61K35/74Bacteria
    • A61K35/741Probiotics
    • A61K35/744Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
    • A61K35/745Bifidobacteria
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66Microorganisms or materials therefrom
    • A61K35/74Bacteria
    • A61K35/741Probiotics
    • A61K35/744Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
    • A61K35/747Lactobacilli, e.g. L. acidophilus or L. brevis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20Bacteria; Culture media therefor
    • C12N1/205Bacterial isolates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K2035/11Medicinal preparations comprising living procariotic cells
    • A61K2035/115Probiotics
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12RINDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/01Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12RINDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/01Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/225Lactobacillus
    • C12R2001/23Lactobacillus acidophilus
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12RINDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/01Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/225Lactobacillus
    • C12R2001/245Lactobacillus casei
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P60/00Technologies relating to agriculture, livestock or agroalimentary industries
    • Y02P60/80Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
    • Y02P60/87Re-use of by-products of food processing for fodder production

Definitions

  • the invention relate to use of probiotic bacteria for the manufacture of a food product, feed product, dietary supplement, nutritional product, natural remedy, pharmaceutical active formulation and medicinal product to be used for controlling weight gain, preventing obesity, increasing satiety, prolonging satiation, reducing food intake, reducing fat deposition, improving energy metabolism, enhancing insulin sensitivity, treating obesity and treating insulin insensitivity.
  • Probiotics are defined by ILSE (International life science institute) as added "microorganisms with a beneficial effect on health”. Probiotics are commonly used in foods, feed products and dietary supplements for their influence on gut health, infection and the immunsystem. Some probiotic strains, but not all studied, have also been shown to influence blood cholesterol level and recently the possibility to lower blood pressure by the use of milk products fermented by proteolytic lactic acid bacteria has been found. Thus the interest in probiotics is wide and the central role of the gut flora for gut health and wellbeing and the immune system is strongly established.
  • ILSE International life science institute
  • glucose metabolism An important factor in the metabolic syndrome is the glucose metabolism including the insulin sensitivity. There is a link between body fat deposition, insulin insensitivity and overweight. There is also a link to satiety and satiation. The interactions and relationships between all those functions are complex and it is difficult to identify the exact sequence of events leading to health or disease.
  • a number of genes and their corresponding proteins that are involved in energy homeostasis have been described. Adipose tissue synthesizes a number of proteins with structural resemblance to cytokines and therefore these proteins are named adipokines. Some of those are also synthesised in the gut or the synthesis is regulated from the gut.
  • the nuclear receptor PPAR-gamma is involved in the synthesis of e.g.
  • adiponectine and the synthesis is associated with calorie intake and leptin signalling.
  • Increased synthesis of adiponectine improves insulin sensitivity by increasing fatty-acid transport, oxidation and dissipation in skeletal muscle and by increasing the sensitivity of the hepatocyte to insulin.
  • Another nutritionally regulated adipocyte-derivied factor influencing insulin sensitivity is resistin. Circulating resistin levels are increased in obesity while treatment of mice with resistin resulted in increased glucose production and impaired insulin action. Thus resistin has a function in glucose homeostasis, and acts as an antagonist to insulin action, giving rise to insulin resistance.
  • Resistin-like proteins are also expressed in the gastrointestinal tract (14). The protein apolipoprotein A-IV is secreted by the small intestine in humans and in rodents. The synthesis is stimulated by fat intake and the protein is probably involved in inhibiting food intake after ingestion of fat.
  • apolipoprotein A-IV probably is involved both in the short-time and long-time regulation of food intake.
  • An object of the invention is use of probiotic bacteria for the manufacture of a food product, feed product, dietary supplement, nutritional product , natural remedy, pharmaceutical active formulation and medicinal products to be used for controlling weight gain, preventing obesity, increasing satiety, prolonging satiation, reducing food intake, reducing fat deposition, improving energy metabolism, enhancing insulin sensitivity, treating obesity and treating insulin insensitivity.
  • probiotic bacteria being selected from the group consistion of lactic acid bacteria specially Lactobacillus casei, Lactobacillus acidophilus, and Bifidobacterium lactis, and more preferably Lactobacillus casei F19 (LMG P- 17806),
  • Lactobacillus acidophilus NCFB 1748, and Bifidobacterium lactis Bbl2 the bacteria are deponated at LMG culture collection in Gent, available from the NCFB culture collection and from Chr. Hansen Company DK, respectively.
  • the strains will be referred to as LMG P- 17806, NCFB 1748 and Bbl2 below.
  • Lactobacillus casei Fl 9 (LMG P- 17806), Lactobacillus acidophilus NCFB 1748, and
  • Bifidobacterium lactis Bbl2 are well characterised and the LMG P-17806 strain and its use is previously patented (WO 99/29833). The three strains survive well in food products and during the passage thrrough the gut.
  • Type II diabetes is caused by a low sensitivity to insulin or insulin resistance. This threat to human health increases continuously in all age groups all over the world. Lactobacilli as probiotics are accepted as a food product and feed product, natural product, dietary supplements, and in natural remedies, pharmaceutical active formulations and medicinal products. They are easy to use in those delivery systems and can easily be consumed on a daily basis.
  • mice After the standard breakfast above and the four hour when data on satiety and hunger were noticed the participants were offered to eat a standard lunch meal. The participants were asked to eat until they were consciously satisfied and to try to get the same level of fullness after each different breakfast. After eating the probiotic products the energy intake at lunch was 3690 KJ for the product with high level of probiotics, it was 3810 for the low level probiotic. For placebo no 1 it was 3850 and for placebo no 2 it vas 3995. This shows that the probiotic products can reduce the energy intake in a postprandial meal after eating the probiotic products as part of the breakfast. 3) Food intake of mice
  • mice of Swiss Webster strain were given acidified milk containing either LMG P-17806 or NCFB 1748 or a placebo product with the same composition but without probiotics for 10 days. The mice were between 6 and 8 weeks when the administration was started.
  • the groups given probiotics contained 7 mice in each group and the placebo group consisted of 5 animals.
  • the probiotic microrganisms were added to the products in final concentration of lxlOE8 CFU/ml and the number of bacteria was stable in the product during the feeding period.
  • the mice were given two standard daily dosages of the products, one by oral gavage feeding of 1 ml and one by sublingual injection. Both probiotic bacteria survived the passage in the gut and were present in significant numbers in the small and large intestine of the mice.
  • mice had ad libitum access to purified ingredient diet (D12450B from Research Diets Inc., New Jersey, USA).
  • the daily food intake was compared between the two groups of mice receiving Lactobacillus strains versus the placebo group of mice. The products were well tolerated by the mice.
  • mice Normal flora mice were given either an acidified milk probiotic product containing LMG P- 17806 or a placebo product with the same composition but without probiotics or kept as a control group given the same feed as the two other groups but without the acidified milk.
  • the mice strain chosen was C57B16 (Charles River) which is sensitive to diet induced obesity.
  • the number of animals included in the different groups was 15 in each of the groups given acidified milk and 3 in the control group. The mice were introduced into the study when they were 9 weeks old.
  • the number of probiotic bacteria in the product was 1x10E8 CFU/ml and the mice were allowed to eat the product ad libitum, 5 days a week, for a total number of 12 weeks.
  • mice were fed with a high fat diet (D 12309 from Research Diets Inc. New Jersey, USA containing 36% fat for the first 5 weeks and then D12492 (35% fat) from the same company for the remaining weeks of the trial). After 12 weeks the mice were sacrificed and the data on weight gain, food consumption and amount of abdominal fat was analysed. The mice given acidified milk product gained less weight than the control mice not receiving any acidified milk. The mice given acidified milk with probiotics also had a lower storage of abdominal fat compared to the group receiving acidified milk without probiotics and the control group not receiving any acidified milk at all.
  • a high fat diet D 12309 from Research Diets Inc. New Jersey, USA containing 36% fat for the first 5 weeks and then D12492 (35% fat) from the same company for the remaining weeks of the trial. After 12 weeks the mice were sacrificed and the data on weight gain, food consumption and amount of abdominal fat was analysed. The mice given acidified milk product gained less weight than the control mice not receiving any acidified milk. The mice given acidified milk
  • mice of Swiss Webster strain were given acidified milk containing either LMG P-17806 or NCFB 1748 or a placebo product with the same composition but without probiotics for 10 days.
  • the mice were between 6 and 8 weeks of age when the administration was started.
  • the groups given probiotics contained 6 mice in each group and the placebo group consisted of 4 animals.
  • the probiotic microrganisms were added to the products in final concentration of lxl0E8 CFU/ml and the number of bacteria was stable in the product during the feeding period.
  • the mice were given the product daily by oral gavage feeding. During the study the mice had ad libitum access to purified ingredient diet (D12450B from Research Diets Inc., New Jersey, USA).
  • the total dosage of the individual strains of probiotic bacteria in the different experiments described above was lxlOE8-lxlOE9 CFU (mice experiments) and 2,5xl0E8-2,5xl0E10 (human experiments).
  • This dosage needs to be administrated in a portion or as a daily dose meaning that e.g. a drink for human use that is consumed in amounts 200-500 ml need to contain 0,5xl0E6-l,25xl0E8 CFU/ml of the individual strain for efficacy and a capsule need to contain the total amount of bacteria in approximately 1 g of the content in the capsule i.e lxl0E8-2,5xl0E10. For the highest concentrations of bacteria the bacteria need to be concentrated by freeze drying or spray drying.
  • the probiotic bacteria have to be added to products based on milk, cereals or fruits.
  • the bacteria were added as a concentrate e.g. lyophilized and the survival has been analysed in all tree matrixes.
  • the survival was very good in milk based and cereal based products.
  • the survival is influenced by the fruit type.
  • the probiotic bacteria can also be added to milk based products together with other lactic acid bacteria for the production of different kinds of cultured products. In this environment the probiotic bacteria can multiply and will be well adjusted to the acid environment giving a good survival also at the low final pH in those products. The results from product production can be seen in table 1.
  • Bojrab G.. 2000 Composition and method for treatment of gastrointestinal disorders and hyperlipedemia. US patent 6 696 057

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PCT/SE2006/001117 2005-10-07 2006-10-02 Probiotics to influence fat metabolism and obesity Ceased WO2007043933A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
PL06799717T PL1945235T3 (pl) 2005-10-07 2006-10-02 Probiotyki wpływające na metabolizm tłuszczu i otyłość
AU2006299956A AU2006299956B2 (en) 2005-10-07 2006-10-02 Probiotics to influence fat metabolism and obesity
ES06799717T ES2396865T3 (es) 2005-10-07 2006-10-02 Probióticos para influenciar el metabolismo de las grasas y la obesidad
JP2008534487A JP2009511469A (ja) 2005-10-07 2006-10-02 脂肪代謝及び肥満に影響を及ぼすプロバイオティクス
EP06799717A EP1945235B1 (en) 2005-10-07 2006-10-02 Probiotics to influence fat metabolism and obesity
CA002624890A CA2624890A1 (en) 2005-10-07 2006-10-02 Probiotics to influence fat metabolism and obesity
EA200800913A EA015461B1 (ru) 2005-10-07 2006-10-02 Применение пробиотических бактерий в пищевых, кормовых и лечебных продуктах
DK06799717.1T DK1945235T3 (da) 2005-10-07 2006-10-02 Probiotika til at påvirke fedtmetabolisme og fedme
SI200631495T SI1945235T1 (sl) 2005-10-07 2006-10-02 Probiotiki, ki vplivajo na presnovo maščob in debelost
BRPI0616993-7A BRPI0616993A2 (pt) 2005-10-07 2006-10-02 bactérias probióticas que influenciam o metabolismo de gordura e obesidade, bem como produtos, capsúlas e uso das mesmas
US12/089,433 US20080267933A1 (en) 2005-10-07 2006-10-02 Probiotics to Influence Fat Metabolism and Obesity
CN2006800368040A CN101287478B (zh) 2005-10-07 2006-10-02 影响脂肪代谢和肥胖的益生菌

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE0502214A SE529185C2 (sv) 2005-10-07 2005-10-07 Användning av probiotiska bakterier för tillverkning av livsmedel eller läkemedel för förhindrande av övervikt
SE0502214-0 2005-10-07

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WO2007043933A1 true WO2007043933A1 (en) 2007-04-19

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PCT/SE2006/001117 Ceased WO2007043933A1 (en) 2005-10-07 2006-10-02 Probiotics to influence fat metabolism and obesity

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US (1) US20080267933A1 (enExample)
EP (2) EP2431044B1 (enExample)
JP (1) JP2009511469A (enExample)
CN (1) CN101287478B (enExample)
AU (1) AU2006299956B2 (enExample)
BR (1) BRPI0616993A2 (enExample)
CA (1) CA2624890A1 (enExample)
CY (1) CY1113704T1 (enExample)
DK (2) DK1945235T3 (enExample)
EA (1) EA015461B1 (enExample)
ES (2) ES2396865T3 (enExample)
PL (1) PL1945235T3 (enExample)
PT (1) PT1945235E (enExample)
SE (1) SE529185C2 (enExample)
SI (1) SI1945235T1 (enExample)
WO (1) WO2007043933A1 (enExample)

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008063289A (ja) * 2006-09-08 2008-03-21 Snow Brand Milk Prod Co Ltd 血中アディポネクチン濃度増加促進及び/又は減少抑制剤
WO2007085970A3 (en) * 2006-01-27 2008-05-08 Danisco Use of probiotic microorganisms for the treatment and prevention of obesity and related disorders
EP2011506A1 (en) * 2007-07-05 2009-01-07 Nestec S.A. Supplementation of maternal diet
WO2009014421A1 (en) * 2007-07-25 2009-01-29 Campina Nederland Holding B.V. Probiotics for inducing satiety and/or satiation
JP2009107956A (ja) * 2007-10-29 2009-05-21 Snow Brand Milk Prod Co Ltd アディポネクチン分泌促進及び/又は減少抑制剤
WO2009071086A3 (en) * 2007-12-06 2009-08-13 Arla Foods Amba Probiotic bacteria and regulation of fat storage
WO2010108950A1 (en) * 2009-03-25 2010-09-30 Chr. Hansen A/S Use of a probiotic to regulate body weight
WO2010108865A1 (en) 2009-03-25 2010-09-30 Chr. Hansen A/S Use of probiotics to ameliorate diet-induced insulin resistance
WO2010146568A2 (en) 2009-06-19 2010-12-23 Danisco A/S Bifidobacteria for treating diabetes and related conditions
WO2010130785A3 (en) * 2009-05-12 2011-01-06 Valio Ltd Novel use of probiotics
US20110123501A1 (en) * 2007-08-17 2011-05-26 Nestec S.A. Gut flora and weight management
JP2011517570A (ja) * 2008-04-18 2011-06-16 コンパニ・ジェルベ・ダノン 抗菌特性及び免疫調節特性を有する新規なラクトバチルス・パラカゼイ亜種パラカゼイ株
WO2011096808A1 (en) 2010-02-05 2011-08-11 Friesland Brands B.V. Use of sialyl oligosaccharides in weight management
EP2359838A1 (fr) 2010-02-02 2011-08-24 Aragan Préparation destinée à traiter l`excès pondéral et les désordres associés et applications de ladite préparation
EP2276344A4 (en) * 2008-05-19 2011-09-14 Nestec Sa METHODS OF LIMITING ABSORPTION OF LIPIDS BY ANIMAL
WO2012076739A1 (es) 2010-12-07 2012-06-14 Consejo Superior De Investigaciones Científicas C.S.I.C. Bifidobacterium CECT 7765 y su uso en la prevención y/o tratamiento del sobrepeso, la obesidad y patologías asociadas
JP2012520292A (ja) * 2009-03-10 2012-09-06 ジニス バイオファーマサティカルズ カンパニー 微生物を利用した肥満及び肥満によって引き起こされた代謝性疾患の予防と治療
WO2014072771A1 (en) 2012-11-12 2014-05-15 Compagnie Gervais Danone Lactobacillus rhamnosus strain for reducing body fat accumulation
US20140286909A1 (en) * 2011-10-18 2014-09-25 Nestec S.A. Composition for use in increasing insulin sensitivity and/or reducing insulin resistance
KR101535077B1 (ko) * 2013-09-13 2015-07-08 주식회사한국야쿠르트 인슐린 저항성 개선 효능을 가지는 비피도박테리움 락티스 hy8101 및 이를 유효성분으로 함유하는 제품
EP2320889A4 (en) * 2008-08-15 2016-09-21 Nestec Sa METHOD FOR INCREASING THE CHANGE OF ENERGY REPLACEMENT
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