法尼甾体X受体
G蛋白偶联胆汁酸受体
非酒精性脂肪肝
医学
核受体
胆汁酸
内科学
内分泌学
脂肪性肝炎
脂肪肝
受体
CYP8B1
胆固醇7α羟化酶
糖尿病
炎症
生物
血脂异常
2型糖尿病
脂质代谢
生物化学
疾病
转录因子
基因
作者
Oscar Chávez‐Talavera,Anne Tailleux,Philippe Lefèbvre,Bart Staels
出处
期刊:Gastroenterology
[Elsevier]
日期:2017-02-15
卷期号:152 (7): 1679-1694.e3
被引量:700
标识
DOI:10.1053/j.gastro.2017.01.055
摘要
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.
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