Phillips M J, Oda M, Funatsu K
Am J Pathol. 1978 Dec;93(3):729-44.
An experimental study of norethandrolone (NED)-induced intrahepatic cholestasis was made. NED was infused via a portal vein catheter into rat liver in vivo, and measurements were made of bile flow. Liver specimens were taken at intervals for light microscopy and for transmission and scanning electron microscopy. Bile-canalicular-rich membrane fractions were prepared. The effects of NED were also examined in isolated hepatocytes in suspension culture. NED infusion induced total cholestasis by 3 hours. Canalicular alterations commonly associated with cholestasis were found in in vivo infused liver and in isolated hepatocytes. Pericanalicular microfilament changes were also noted in both, with loss of filament structure and replacement by a granular zone. In isolated canalicular membrane fractions prepared from NED-treated animals, the normal investment of pericanalicular filaments was no longer present. Loss of the bile canalicular ruthenium red surface coat was also noted. In view of the identical findings in isolated hepatocytes and in in vivo liver, obstruction and mechanical factors can be excluded as possible causes. The results raise the possibility that the mechanism of NED-induced cholestasis may be related to disaggregation and/or detachment of microfilaments from the canalicular membranes.
进行了一项关于炔诺酮(NED)诱导肝内胆汁淤积的实验研究。将NED通过门静脉导管在体内注入大鼠肝脏,并测量胆汁流量。每隔一段时间采集肝脏标本用于光学显微镜检查以及透射和扫描电子显微镜检查。制备富含胆小管的膜部分。还在悬浮培养的分离肝细胞中研究了NED的作用。注入NED 3小时后诱导了完全性胆汁淤积。在体内注入NED的肝脏和分离的肝细胞中发现了通常与胆汁淤积相关的胆小管改变。在两者中还注意到胆小管周围微丝的变化,微丝结构丧失并被颗粒区取代。在从NED处理的动物制备的分离胆小管膜部分中,不再存在胆小管周围微丝的正常包绕。还注意到胆小管钌红表面涂层的丧失。鉴于在分离的肝细胞和体内肝脏中发现相同的结果,可以排除阻塞和机械因素作为可能的原因。结果提示,NED诱导胆汁淤积的机制可能与微丝从胆小管膜的解聚和/或脱离有关。