Laboratory of Experimental and Molecular Hepatology, Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Semin Liver Dis. 2010 May;30(2):160-77. doi: 10.1055/s-0030-1253225. Epub 2010 Apr 26.
Although hereditary or acquired defects in hepatobiliary transporter systems cause or predispose to cholestasis, adaptive bile acid transporter changes can counteract cholestasis by reducing hepatocellular and systemic concentrations of retained cholephiles. An important level in the regulation of adaptive bile acid transporters and overflow pathways is mediated at the transcriptional level by nuclear hormone receptors. Moreover, therapeutic approaches targeting nuclear receptors in cholestasis may stimulate these adaptive changes and open a new perspective for the treatment of cholestatic liver diseases. This review gives a comprehensive overview on bile acid transporters in the enterohepatic circulation and their adaptive changes in response to cholestasis as well as the regulatory networks underlying these adaptive mechanisms.
尽管肝胆转运系统的遗传或获得性缺陷导致或易患胆汁淤积症,但适应性胆汁酸转运体的变化可以通过降低肝细胞和全身滞留胆质浓度来对抗胆汁淤积症。核激素受体在转录水平上调节适应性胆汁酸转运体和溢出途径的重要水平。此外,针对胆汁淤积症核受体的治疗方法可能会刺激这些适应性变化,为治疗胆汁淤积性肝病开辟新的视角。本综述全面概述了肠肝循环中的胆汁酸转运体及其对胆汁淤积症的适应性变化,以及这些适应性机制的调节网络。