肝肠循环
胆汁酸
胆汁淤积
核受体
生物
肝X受体
胆结石
内科学
内分泌学
生物化学
医学
转录因子
基因
作者
Emina Halilbasic,Thierry Claudel,Michael Trauner
标识
DOI:10.1016/j.jhep.2012.08.002
摘要
Bile acid (BA) transporters are critical for maintenance of the enterohepatic BA circulation where BAs exert their multiple physiological functions including stimulation of bile flow, intestinal absorption of lipophilic nutrients, solubilization and excretion of cholesterol, as well as antimicrobial and metabolic effects. Tight regulation of BA transporters via nuclear receptors is necessary to maintain proper BA homeostasis. Hereditary and acquired defects of BA transporters are involved in the pathogenesis of several hepatobiliary disorders including cholestasis, gallstones, fatty liver disease and liver cancer, but also play a role in intestinal and metabolic disorders beyond the liver. Thus, pharmacological modification of BA transporters and their regulatory nuclear receptors opens novel treatment strategies for a wide range of disorders.
科研通智能强力驱动
Strongly Powered by AbleSci AI