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Bile Acids as Hormones: The FXR-FGF15/19 Pathway

机译:胆汁酸作为激素:FXR-FGF15 / 19途径

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摘要

While it has long been recognized that bile acids are essential for solubilizing lipophilic nutrients in the small intestine, the discovery in 1999 that bile acids serve as ligands for the nuclear receptor FXR opened the floodgates in terms of characterizing their actions as selective signaling molecules. Bile acids act on FXR in ileal enterocytes to induce the expression of fibroblast growth factor (FGF) 15/19, an atypical FGF that functions as a hormone. FGF15/19 subsequently acts on a cell surface receptor complex in hepatocytes to repress bile acid synthesis and gluconeogenesis and to stimulate glycogen and protein synthesis. FGF15/19 also stimulates gallbladder filling. Thus, the bile acid-FXR-FGF15/19 signaling pathway regulates diverse aspects of the postprandial enterohepatic response. Pharmacologically, this endocrine pathway provides exciting new opportunities for treating metabolic disease and bile acid-related disorders such as primary biliary cirrhosis and bile acid diarrhea. Both FXR agonists and FGF19 analogs are currently in clinical trials.
机译:尽管人们早已认识到胆汁酸对于溶解小肠中的亲脂性营养至关重要,但在1999年发现胆汁酸作为核受体FXR的配体后,就发现了胆汁酸开启了闸门,因为它们将其作用表征为选择性信号分子。胆汁酸作用于回肠肠上皮细胞的FXR,以诱导成纤维细胞生长因子(FGF)15/19的表达,这是一种非典型的FGF,起着激素的作用。 FGF15 / 19随后作用于肝细胞中的细胞表面受体复合物,以抑制胆汁酸合成和糖异生,并刺激糖原和蛋白质合成。 FGF15 / 19还刺激胆囊充盈。因此,胆汁酸-FXR-FGF15 / 19信号通路调节餐后肠肝反应的各个方面。在药理学上,这种内分泌途径为治疗代谢性疾病和与胆汁酸有关的疾病(如原发性胆汁性肝硬化和胆汁酸腹泻)提供了令人兴奋的新机会。 FXR激动剂和FGF19类似物目前都在临床试验中。

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