Short-Chain Fatty Acids Stimulate Glucagon-Like Peptide-1 Secretion via the G-Protein-Coupled Receptor FFAR2

被引:2140
作者
Tolhurst, Gwen [1 ]
Heffron, Helen [2 ]
Lam, Yu Shan [1 ]
Parker, Helen E. [1 ]
Habib, Abdella M. [1 ]
Diakogiannaki, Eleftheria [1 ]
Cameron, Jennifer [2 ]
Grosse, Johannes [2 ]
Reimann, Frank [1 ]
Gribble, Fiona M. [1 ]
机构
[1] Addenbrookes Hosp, Cambridge Inst Med Res, Cambridge, England
[2] Takeda Cambridge Ltd, Cambridge, England
基金
英国惠康基金;
关键词
FUNCTIONAL-CHARACTERIZATION; RESISTANT STARCH; HUMAN COLON; GPR41; RAT; ACETATE; GLP-1; YY; IDENTIFICATION; PROPIONATE;
D O I
10.2337/db11-1019
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Interest in how the gut microbiome can influence the metabolic state of the host has recently heightened. One postulated link is bacterial fermentation of "indigestible" prebiotics to short-chain fatty acids (SCFAs), which in turn modulate the release of gut hormones controlling insulin release and appetite. We show here that SCFAs trigger secretion of the incretin hormone glucagon-like peptide (GLP)-1 from mixed colonic cultures in vitro. Quantitative PCR revealed enriched expression of the SCFA receptors ffar2 (g7p43) and ffar3 (gpr41) in GLP-1 secreting L cells, and consistent with the reported coupling of GPR43 to Gq signaling pathways, SCFAs raised cytosolic Ca(2+) in L cells in primary culture. Mice lacking ffar2 or ffar3 exhibited reduced SCFA-triggered GLP-1 secretion in vitro and in vivo and a parallel impairment of glucose tolerance. These results highlight SCFAs and their receptors as potential targets for the treatment of diabetes. Diabetes 61:364-371, 2012
引用
收藏
页码:364 / 371
页数:8
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