Effects of valproate on xenobiotic biotransformation in rat liver. In vivo and in vitro experiments.

V Rogiers, A Callaerts, A Vercruysse, M Akrawi, E Shephard, I Phillips
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引用次数: 9

Abstract

Male Wistar rats were in vivo exposed for 2 weeks to 100 micrograms/ml sodium valproate by subcutaneous implantation of osmotic pumps and hepatocytes were isolated. As an in vitro model co-cultures of rat hepatocytes with epithelial cells were daily treated with valproate (25, 50, 100, 200 micrograms/ml) for 2 weeks. In both models the cytochrome P-450 content and the enzymatic activities of 7-ethoxycoumarin O-deethylase, aldrin epoxidase and glutathione S-transferase were determined in valproate-treated hepatocytes, in controls and in phenobarbital-induced cells. It appeared that in both systems the cytochrome P-450 content and the 7-ethoxycoumarin O-deethylase activity increased significantly after valproate treatment. On the other hand, the activities of aldrin epoxidase and glutathione S-transferase decreased. A cDNA probe, encoding rat P450IIB2 was used to determine whether mRNAs encoding the P450IIB subfamily were induced by valproate. It became clear that the inducing effect of valproate was even more pronounced in vitro than in vivo.

丙戊酸酯对大鼠肝脏外源性生物转化的影响。体内和体外实验。
通过渗透泵皮下植入100微克/毫升丙戊酸钠,使雄性Wistar大鼠体内暴露2周,分离肝细胞。作为体外模型,每天用丙戊酸盐(25、50、100、200微克/毫升)处理大鼠肝细胞与上皮细胞共培养2周。在两种模型中,分别测定丙戊酸处理的肝细胞、对照组和苯巴比妥诱导的肝细胞中细胞色素P-450的含量以及7-乙氧基香豆素o -去乙基化酶、艾氏醇环氧化酶和谷胱甘肽s -转移酶的酶活性。丙戊酸处理后,两种体系细胞色素P-450含量和7-乙氧基香豆素o -去乙基酶活性均显著升高。另一方面,aldrin环氧化酶和谷胱甘肽s -转移酶活性降低。使用编码大鼠P450IIB2的cDNA探针来确定编码P450IIB亚家族的mrna是否被丙戊酸盐诱导。很明显,丙戊酸的诱导作用在体外比在体内更明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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