Vu D D, Tuchweber B, Plaa G L, Yousef I M
Department of Pharmacology and Nutrition, Université de Montréal, Québec, Canada.
Toxicol Lett. 1992 Jul;61(2-3):255-64. doi: 10.1016/0378-4274(92)90152-a.
The possible relevance of alterations in intracellular Ca2+ and hepatic glutathione levels (GSH) in the pathogenesis of cholestasis induced by lithocholic acid (LCA) was examined by comparing effects of LCA and acetaminophen on these parameters and bile flow (BF) in rats. Intracellular Ca2+ activity was measured via glycogen phosphorylase a determination in rats given an intravenous bolus injection of either LCA (12 mumol/100 g body wt.), acetaminophen (60 mg/100 g body wt.), or a mixed solution of LCA and acetaminophen. BF was reduced immediately after LCA administration, with a maximum decrease occurring at 60 min followed by an increase to normal values at 210 min. On the other hand, glycogen phosphorylase a activity was elevated during all time periods after LCA treatment. Hepatic glutathione followed the BF curves being markedly depleted at the peak of cholestasis (60 min) and normal in the total recovery period (210 min). In contrast, acetaminophen had no effect on BF but significantly increased glycogen phosphorylase a activity and depleted hepatic glutathione levels. These results suggest that cholestatic effect of LCA is not due to changes in intracellular Ca2+ or hepatic glutathione levels.
通过比较石胆酸(LCA)和对乙酰氨基酚对大鼠细胞内钙离子(Ca2+)、肝脏谷胱甘肽水平(GSH)以及胆汁流量(BF)的影响,研究了细胞内Ca2+和肝脏GSH水平变化在LCA诱导胆汁淤积发病机制中的潜在相关性。通过测定给予静脉推注LCA(12 μmol/100 g体重)、对乙酰氨基酚(60 mg/100 g体重)或LCA与对乙酰氨基酚混合溶液的大鼠糖原磷酸化酶a活性,来测量细胞内Ca2+活性。LCA给药后BF立即降低,60分钟时降至最大降幅,随后在210分钟时升至正常值。另一方面,LCA处理后的所有时间段内糖原磷酸化酶a活性均升高。肝脏谷胱甘肽水平随BF曲线变化,在胆汁淤积高峰(60分钟)时显著降低,在完全恢复期(210分钟)时恢复正常。相比之下,对乙酰氨基酚对BF无影响,但显著增加糖原磷酸化酶a活性并降低肝脏谷胱甘肽水平。这些结果表明,LCA的胆汁淤积作用并非由于细胞内Ca2+或肝脏谷胱甘肽水平的变化。