Laboratory of Integrative and Systems Physiology at the Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Dig Dis. 2011;29(1):37-44. doi: 10.1159/000324126. Epub 2011 Jun 17.
Bile acids (BAs) are amphipathic molecules that facilitate the uptake of lipids, and their levels fluctuate in the intestines as well as in the circulation depending on food intake. Besides their role in dietary lipid absorption, BAs function as signaling molecules that activate specific BA receptors and trigger downstream signaling cascades. The BA receptors and the signaling pathways they control are not only important in the regulation of BA synthesis and their metabolism, but they also regulate glucose homeostasis, lipid metabolism and energy expenditure - processes relevant in the context of the metabolic syndrome. In addition to the function of the nuclear receptor FXRα in regulating local effects of BAs in the organs of the enterohepatic axis, increasing evidence points to a crucial role of the G-protein-coupled receptor TGR5 in mediating systemic actions of BAs. Here we review the current knowledge on BA receptors, with a strong focus on the cell membrane receptor TGR5, which has emerged as a promising target for intervention in metabolic diseases.
胆汁酸(BAs)是两亲性分子,有助于脂质的吸收,其水平在肠道和循环中随食物摄入而波动。除了在膳食脂质吸收中的作用外,BAs 还作为信号分子,激活特定的 BA 受体并触发下游信号级联反应。BA 受体及其控制的信号通路不仅在调节 BA 合成及其代谢中很重要,而且还调节葡萄糖稳态、脂质代谢和能量消耗 - 这些过程与代谢综合征有关。除了核受体 FXRα 在调节肠肝轴器官中 BAs 的局部作用的功能外,越来越多的证据表明 G 蛋白偶联受体 TGR5 在介导 BAs 的全身作用中起着关键作用。在这里,我们回顾了 BA 受体的现有知识,重点介绍了细胞膜受体 TGR5,它已成为干预代谢疾病的有希望的靶点。