关键词: Bile canaliculus Bile ducts Bile secretion Cholangiopathies Cholangitis Primary biliary cholangitis Primary sclerosing cholangitis

Mesh : ATP Binding Cassette Transporter, Subfamily B / physiology ATP Binding Cassette Transporter, Subfamily B, Member 11 / physiology Animals Apoptosis Autophagy Bile Acids and Salts / physiology Carrier Proteins / physiology Cholestasis / etiology Humans Liver / pathology Liver Cirrhosis / etiology Membrane Glycoproteins / physiology Mice ATP-Binding Cassette Sub-Family B Member 4

来  源:   DOI:10.1016/j.jhep.2017.04.026   PDF(Sci-hub)

Abstract:
The main trigger for liver injury in acquired cholestatic liver disease remains unclear. However, the accumulation of bile acids (BAs) undoubtedly plays a role. Recent progress in deciphering the pathomechanisms of inborn cholestatic liver diseases, decoding mechanisms of BA-induced cell death, and generating modern BA-derived drugs has improved the understanding of the regulation of BA synthesis and transport. Now is the appropriate time to reassess current knowledge about the specific role of BAs in hepatobiliary injury.
摘要:
获得性胆汁淤积性肝病肝损伤的主要诱因仍不清楚。然而,胆汁酸(BA)的积累无疑起着一定的作用。先天性胆汁淤积性肝病发病机制的研究进展,BA诱导细胞死亡的解码机制,现代BA衍生药物的产生提高了对BA合成和运输调控的认识。现在是重新评估有关BA在肝胆损伤中的具体作用的最新知识的适当时机。
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