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三甲双酮作为评估正常及α-萘基异硫氰酸酯中毒大鼠肝脏药物代谢能力的模型药物。

Trimethadione as a model drug for the evaluation of hepatic drug-metabolizing capacity in normal and alpha-naphthylisothiocyanate-intoxicated rats.

作者信息

Tanaka E, Kinoshita H, Yoshida T, Kuroiwa Y

出版信息

Pharmacology. 1982;25(4):202-9. doi: 10.1159/000137743.

Abstract

The relationship between the plasma concentration ratio of 5,5-dimethyl-2,4-oxazolidinedione (DMO) to trimethadione (TMO) and cytochrome P-450-dependent drug-metabolizing enzyme activities in rats pretreated with different dose levels of alpha-naphthylisothiocyanate (ANIT) was investigated. Pretreatment of rats with different dose levels of ANIT resulted in a prolongation of TMO half-life, an increase of the area under the curve (AUC), a decrease of clearance (CL) and a decrease of the apparent volume of distribution (Vd). At any dose of ANIT used, there was a good correlation between the ratio of DMO to TMO in plasma and activities of hepatic cytochrome P-450-dependent drug-metabolizing enzymes, such as cytochrome P-450 and cytochrome b5 contents and aminopyrine N-demethylase, TMO N-demethylase and aniline hydroxylase. These results, together with the previous findings, indicate that determination of the plasma levels of TMO and DMO might be a useful index of drug-metabolizing capacity of the liver.

摘要

研究了用不同剂量的α-萘异硫氰酸酯(ANIT)预处理的大鼠中,5,5-二甲基-2,4-恶唑烷二酮(DMO)与三甲双酮(TMO)的血浆浓度比与细胞色素P-450依赖性药物代谢酶活性之间的关系。用不同剂量的ANIT预处理大鼠导致TMO半衰期延长、曲线下面积(AUC)增加、清除率(CL)降低和表观分布容积(Vd)减小。在使用的任何剂量的ANIT下,血浆中DMO与TMO的比值与肝细胞色素P-450依赖性药物代谢酶的活性之间都有良好的相关性,如细胞色素P-450和细胞色素b5含量以及氨基比林N-脱甲基酶、TMO N-脱甲基酶和苯胺羟化酶。这些结果与先前的研究结果一起表明,测定TMO和DMO的血浆水平可能是肝脏药物代谢能力的一个有用指标。

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