Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011 - EGID, F-59000 Lille, France.
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011 - EGID, F-59000 Lille, France.
Gastroenterology. 2017 May;152(7):1679-1694.e3. doi: 10.1053/j.gastro.2017.01.055. Epub 2017 Feb 15.
Bile acids are signaling molecules that coordinately regulate metabolism and inflammation via the nuclear farnesoid X receptor (FXR) and the Takeda G protein-coupled receptor 5 (TGR5). These receptors activate transcriptional networks and signaling cascades controlling the expression and activity of genes involved in bile acid, lipid and carbohydrate metabolism, energy expenditure, and inflammation by acting predominantly in enterohepatic tissues, but also in peripheral organs. In this review, we discuss the most recent findings on the inter-organ signaling and interplay with the gut microbiota of bile acids and their receptors in meta-inflammation, with a focus on their pathophysiologic roles in obesity, type 2 diabetes, dyslipidemia, and nonalcoholic steatohepatitis, and their potential therapeutic applications.
胆汁酸是信号分子,通过核法尼醇 X 受体 (FXR) 和 Takeda G 蛋白偶联受体 5 (TGR5) 协调调节代谢和炎症。这些受体通过主要在肠肝组织中,也在周围器官中作用,激活转录网络和信号级联,控制参与胆汁酸、脂质和碳水化合物代谢、能量消耗和炎症的基因的表达和活性。在这篇综述中,我们讨论了胆汁酸及其受体在代谢炎症中的器官间信号传递和与肠道微生物组的相互作用的最新发现,重点是它们在肥胖、2 型糖尿病、血脂异常和非酒精性脂肪性肝炎中的病理生理作用,以及它们的潜在治疗应用。