4.7 Article

Oral treatment with Eubacterium hallii improves insulin sensitivity in db/db mice

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NPJ BIOFILMS AND MICROBIOMES
卷 2, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/npjbiofilms.2016.9

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资金

  1. Swedish Research Council
  2. Swedish Diabetes Foundation
  3. Swedish Heart Lung Foundation
  4. Swedish Foundation for Strategic Research
  5. Knut and Alice Wallenberg foundation
  6. Goran Gustafsson Foundation
  7. Ingbritt and Arne Lundberg's foundation
  8. Torsten Soderberg's Foundation
  9. Ragnar Soderberg's Foundation
  10. NovoNordisk Foundation
  11. AFA insurances
  12. LUA-ALF grants from Vastra Gotalandsregionen and Stockholm County Council
  13. ERC [615362-METABASE]
  14. Finland Academy of Sciences [137389, 141140, 1272870]
  15. Netherlands Organization for Scientific Research [024.002.002]
  16. European Research Council (ERC) [250172]
  17. ZONMW-VIDI grant [016.146.327]

向作者/读者索取更多资源

An altered intestinal microbiota composition is associated with insulin resistance and type 2 diabetes mellitus. We previously identified increased intestinal levels of Eubacterium hallii, an anaerobic bacterium belonging to the butyrate-producing Lachnospiraceae family, in metabolic syndrome subjects who received a faecal transplant from a lean donor. To further assess the effects of E. hallii on insulin sensitivity, we orally treated obese and diabetic db/db mice with alive E. hallii and glycerol or heat-inactive E. hallii as control. Insulin tolerance tests and hyperinsulinemic-euglycemic clamp experiments revealed that alive E. hallii treatment improved insulin sensitivity compared control treatment. In addition, E. hallii treatment increased energy expenditure in db/db mice. Active E. hallii treatment was found to increase faecal butyrate concentrations and to modify bile acid metabolism compared with heat-inactivated controls. Our data suggest that E. hallii administration potentially alters the function of the intestinal microbiome and that microbial metabolites may contribute to the improved metabolic phenotype.

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