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首页> 外文期刊>The biochemical journal >The effect of colchicine on the development of lithocholic acid-induced cholestasis. A study of the role of microtubules in intracellular cholesterol transport
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The effect of colchicine on the development of lithocholic acid-induced cholestasis. A study of the role of microtubules in intracellular cholesterol transport

机译:秋冬酸血清酸诱导胆汁淤积的影响。微管在细胞内胆固醇转运中的作用研究

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pThe 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./p
机译:>锂色酸(LCA-NA)诱导的胆汁淤积的发病机制涉及胆汁疱疹在胆汁釜膜中的快速积累。由于微管在许多材料的细胞内运输中起重要作用,因此本研究旨在评估它们参与LCA-Na诱导的胆汁淤积的发展程度。在用LCA-Na(12mumol / 100g体重量)中注射后90分钟,将大鼠预处理了大鼠(0.2mumol / 100g体积%)或盐水溶液。血清曲霉虽然没有增加胆汁流动,但显着降低了LCA-NA引起的胆汁淤积(胆汁流量57-32%),而不会影响其新陈代谢在血液,肝脏或胆汁中的血液,肝脏或胆汁中的分布。从用秋天的组合和LCA-NA组合处理的胆汁管膜含有较少的胆固醇,而不是用LCA-Na处理的那些。然而,从单独用血清晶氨酸处理的大鼠获得的膜含有比对照更少的胆固醇。结果发现,通过血红素处理不变,在LCA-Na处理后,在LCA-Na处理后累积在LCA-Na处理后的胆汁管膜中的胆固醇总量(LCA-Na + Colcocine与狼藤曲霉相比)。鉴于这些发现,建议胆汁膜内存在的胆固醇总量决定了LCA-Na诱导的胆汁淤积的程度,LCA-Na可能通过微管型途径和微管移动胆固醇到胆汁釜膜。不太可能在LCA-Na的型横细胞传输中起作用。

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