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肠道法尼醇X受体和武田G蛋白偶联受体5信号通路在代谢调节中的作用

Intestinal Farnesoid X Receptor and Takeda G Protein Couple Receptor 5 Signaling in Metabolic Regulation.

作者信息

Chiang John Y L, Pathak Preeti, Liu Hailiang, Donepudi Ajay, Ferrell Jessica, Boehme Shannon

机构信息

Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, Ohio, USA.

出版信息

Dig Dis. 2017;35(3):241-245. doi: 10.1159/000450981. Epub 2017 Mar 1.

Abstract

Bile acids play a critical role in the regulation of glucose, lipid and energy metabolisms by activating the nuclear bile acid receptor farnesoid X receptor (FXR) and membrane G protein-coupled bile acid receptor-1 (aka takeda G protein couple receptor 5, TGR5) signaling. Paradoxical roles of FXR in the regulation of glucose and lipid metabolism and metabolic disorder have been reported recently. The activation or inhibition of intestinal FXR signaling has been shown to improve insulin and glucose sensitivity and energy metabolism to prevent diabetes, obesity and non-alcoholic fatty liver disease (NAFLD). TGR5 has an anti-inflammatory function in the intestine and stimulates glucagon-like peptide-1 (GLP-1) secretion in the intestine to stimulate insulin secretion from the pancreas. The role of TGR5 in metabolism and metabolic regulation is not clear and warrants further study. FXR and TGR5 are co-expressed in the ileum and colon. These 2 bile acid-activated receptors may cooperate to stimulate GLP-1 secretion and improve hepatic metabolism. FXR and TGR5 dual agonists may have therapeutic potential for treating diabetes and NAFLD.

摘要

胆汁酸通过激活核胆汁酸受体法尼醇X受体(FXR)和膜G蛋白偶联胆汁酸受体-1(又名武田G蛋白偶联受体5,TGR5)信号通路,在葡萄糖、脂质和能量代谢的调节中发挥关键作用。最近有报道称FXR在葡萄糖和脂质代谢及代谢紊乱的调节中具有矛盾的作用。已表明激活或抑制肠道FXR信号通路可改善胰岛素和葡萄糖敏感性以及能量代谢,从而预防糖尿病、肥胖症和非酒精性脂肪性肝病(NAFLD)。TGR5在肠道中具有抗炎功能,并刺激肠道中胰高血糖素样肽-1(GLP-1)的分泌,从而刺激胰腺分泌胰岛素。TGR5在代谢和代谢调节中的作用尚不清楚,值得进一步研究。FXR和TGR5在回肠和结肠中共同表达。这两种胆汁酸激活受体可能协同刺激GLP-1分泌并改善肝脏代谢。FXR和TGR5双重激动剂可能具有治疗糖尿病和NAFLD的潜力。

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