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秋水仙碱对石胆酸诱导的胆汁淤积发展的影响。关于微管在细胞内胆固醇转运中作用的研究。

The effect of colchicine on the development of lithocholic acid-induced cholestasis. A study of the role of microtubules in intracellular cholesterol transport.

作者信息

Barnwell S G, Yousef I M, Tuchweber B

出版信息

Biochem J. 1986 Jun 1;236(2):345-50. doi: 10.1042/bj2360345.

Abstract

The pathogenesis of lithocholic acid (LCA-Na)-induced cholestasis involves a rapid accumulation of cholesterol in the bile canalicular membrane. Since microtubules play an important role in the intracellular transport of many materials, including cholesterol, the present study was undertaken to assess the extent to which they participate in the development of LCA-Na-induced cholestasis. Rats were pretreated with either colchicine (0.2 mumol/100 g body wt.) or saline solution 90 min before injection with LCA-Na (12 mumol/100 g body wt.). Colchicine, although not increasing bile flow by itself, significantly reduced the cholestasis caused by LCA-Na (57-32% reduction in bile flow) without affecting its metabolism into less toxic bile acids or its distribution in blood, liver or bile. Bile canalicular membranes isolated from animals treated with a combination of colchicine and LCA-Na contained less cholesterol than those treated with LCA-Na alone. However, membranes obtained from rats treated with colchicine alone contained much less cholesterol than did controls. It was found that the total amount of cholesterol accumulated within the bile canalicular membrane following LCA-Na treatment (LCA-Na + colchicine versus colchicine alone compared with LCA-Na versus controls) was unchanged by colchicine treatment. In view of these findings it is suggested that the total amount of cholesterol present within the bile canalicular membrane determines the extent of LCA-Na-induced cholestasis, LCA-Na probably moves cholesterol to the bile canalicular membrane via a microtubule independent pathway, and microtubules are unlikely to function in the transcellular transport of LCA-Na.

摘要

石胆酸(LCA-Na)诱导胆汁淤积的发病机制涉及胆固醇在胆小管膜中的快速积累。由于微管在包括胆固醇在内的许多物质的细胞内运输中起重要作用,因此进行本研究以评估它们在LCA-Na诱导的胆汁淤积发展过程中的参与程度。在注射LCA-Na(12 μmol/100 g体重)前90分钟,用秋水仙碱(0.2 μmol/100 g体重)或盐溶液对大鼠进行预处理。秋水仙碱虽然本身不会增加胆汁流量,但能显著减轻LCA-Na引起的胆汁淤积(胆汁流量减少57%-32%),而不影响其代谢为毒性较小的胆汁酸或其在血液、肝脏或胆汁中的分布。从用秋水仙碱和LCA-Na联合处理的动物中分离出的胆小管膜所含胆固醇比仅用LCA-Na处理的动物少。然而,单独用秋水仙碱处理的大鼠获得的膜所含胆固醇比对照组少得多。研究发现,秋水仙碱处理并未改变LCA-Na处理后(LCA-Na + 秋水仙碱与单独秋水仙碱相比,LCA-Na与对照组相比)胆小管膜内积累的胆固醇总量。鉴于这些发现,提示胆小管膜内存在的胆固醇总量决定了LCA-Na诱导的胆汁淤积程度,LCA-Na可能通过一条不依赖微管的途径将胆固醇转运至胆小管膜,并且微管不太可能在LCA-Na的跨细胞运输中发挥作用。

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