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卡马西平可诱导大鼠体内多种细胞色素P450亚家族。

Carbamazepine induces multiple cytochrome P450 subfamilies in rats.

作者信息

Tateishi T, Asoh M, Nakura H, Watanabe M, Tanaka M, Kumai T, Kobayashi S

机构信息

Department of Pharmacology, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.

出版信息

Chem Biol Interact. 1999 Feb 12;117(3):257-68. doi: 10.1016/s0009-2797(98)00110-0.

Abstract

We compared the effect of three different doses (30, 60, and 100 mg/kg) of carbamazepine (CBZ) administered intraperitoneally for 1, 3, and 7 days on the activity and protein content of hepatic cytochrome P450 (CYP) subfamilies in Sprague-Dawley rats. After 3-day- and 7-day administration with CBZ, the total CYP content had increased in a dose-dependent fashion. Among six enzyme activities examined, only aniline hydroxylase activity remained unchanged after 7-day treatment with CBZ. Pentoxyresorufin O-deethylase activity showed the most significant increase and was induced up to 7 days in a time-dependent fashion. Pretreatment of rats with cycloheximide significantly suppressed the pentoxyresorufin O-deethylase induction by one dose of 100 mg/day CBZ. Immunoblot analysis showed a significant correlation between the protein content of each isoenzyme examined and its activity except CYP2E1 after 7-day treatment with CBZ. Similar results were obtained in the mRNA levels of CYP subfamilies. These results suggested that CBZ may induce multiple CYP subfamilies, except CYP2E1, and the activity and the protein content of CYP2B showed the greatest increase with increased CYP2B mRNA.

摘要

我们比较了腹腔注射三种不同剂量(30、60和100毫克/千克)的卡马西平(CBZ)1天、3天和7天对Sprague-Dawley大鼠肝脏细胞色素P450(CYP)亚家族活性和蛋白质含量的影响。用CBZ给药3天和7天后,总CYP含量呈剂量依赖性增加。在所检测的六种酶活性中,用CBZ处理7天后只有苯胺羟化酶活性保持不变。戊氧基试卤灵O-脱乙基酶活性增加最为显著,并在7天内呈时间依赖性诱导。用环己酰亚胺预处理大鼠可显著抑制100毫克/天单剂量CBZ对戊氧基试卤灵O-脱乙基酶的诱导作用。免疫印迹分析表明,用CBZ处理7天后,除CYP2E1外,所检测的每种同工酶的蛋白质含量与其活性之间存在显著相关性。在CYP亚家族的mRNA水平上也得到了类似的结果。这些结果表明,CBZ可能诱导除CYP2E1外的多个CYP亚家族,并且CYP2B的活性和蛋白质含量随着CYP2B mRNA的增加而增加最为显著。

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