Lee J, Boyer J L
Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520-8019, USA.
Semin Liver Dis. 2000;20(3):373-84. doi: 10.1055/s-2000-9390.
Recent advances in the molecular cloning of membrane transport systems that determine bile formation have facilitated studies of the molecular mechanisms of cholestatic liver disease. The present review summarizes what has been learned about the molecular alterations of these membrane transporters in hepatocytes and cholangiocytes in acquired cholestatic liver disorders. Much of this information has been obtained from the study of animal models of cholestasis and from more limited studies in clinical cholestatic liver diseases. Many of these responses may be interpreted as adaptations that serve to diminish cholestatic liver injury.
决定胆汁形成的膜转运系统分子克隆方面的最新进展,推动了对胆汁淤积性肝病分子机制的研究。本综述总结了在获得性胆汁淤积性肝病中,肝细胞和胆管细胞内这些膜转运体分子改变的相关研究成果。这些信息大多来自胆汁淤积动物模型的研究以及临床胆汁淤积性肝病的有限研究。其中许多反应可被视为旨在减轻胆汁淤积性肝损伤的适应性变化。