Gut microbiota and GLP-1

被引:274
作者
Everard, Amandine [1 ]
Cani, Patrice D. [1 ]
机构
[1] Catholic Univ Louvain, Louvain Drug Res Inst, Metab & Nutr Res Grp, WELBIO Walloon Excellence Life Sci & BIOtechnol, B-1200 Brussels, Belgium
基金
欧洲研究理事会;
关键词
Gut microbiota; GLP-1; L-cells; Endocannabinoids; Prebiotics; GLUCAGON-LIKE PEPTIDE-1; PROTEIN-COUPLED RECEPTOR; CHAIN FATTY-ACIDS; DIETARY-RESISTANT STARCH; OLIGOFRUCTOSE PROMOTES SATIETY; LARGE-BOWEL FERMENTATION; COLONIC FERMENTATION; INTESTINAL MICROBIOTA; ENTEROENDOCRINE CELLS; APPETITE REGULATION;
D O I
10.1007/s11154-014-9288-6
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
A large body of evidence suggests that the regulation of energy balance and glucose homeostasis by fermentable carbohydrates induces specific changes in the gut microbiota. Among the mechanisms, our research group and others have demonstrated that the gut microbiota fermentation (i.e., bacterial digestion of specific compounds) of specific prebiotics or other non-digestible carbohydrates is associated with the secretion of enteroendocrine peptides, such as the glucagon-like peptide-1 (GLP-1) and peptide YY (PYY), produced by L-cells. In this review, we highlight past and recent results describing how dietary manipulation of the gut microbiota, using nutrients or specific microbes, can stimulate GLP-1 secretion in rodents and humans. Furthermore, the purpose of this review is to discuss the putative mechanisms by which specific bacterial metabolites, such as short chain fatty acids, trigger GLP-1 secretion through GPR41/43-dependent mechanisms. Moreover, we conclude by discussing the molecular advance showing that the endocannabinoid system or related bioactive lipids modulated by the gut microbiota may contribute to the regulation of glucose, lipid and energy homeostasis.
引用
收藏
页码:189 / 196
页数:8
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