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中药与西药在大鼠体内的相互作用——茵陈蒿汤与对乙酰氨基酚

Interaction between traditional Chinese medicine and Western medicine in rats--In-Chen-How and acetaminophen.

作者信息

Chan Agnes L F, Liu Wen-Te, Lin Shun-Jin, Leung Henry W C, Wang Hue-Yue

机构信息

Department of Pharmacy, Chi Mei Medical Center, Tainan Taiwan, China.

出版信息

Yao Xue Xue Bao. 2007 Mar;42(3):342-6.

Abstract

The purpose of this study is to evaluate the interaction effects of In-Chen-How (Artemisia capillaries Thunb.) on the pharmacokinetics of acetaminophen and on liver microsomal cytochrome P450 enzyme activity in rats. The rats were divided into control group (n = 8) without In-Chen-How and the pretreated group (n = 8) administered with In-Chen-How (approximately 1.0 mL x kg(-1), according to weight) for 5 consecutive days. Rats in the control group received water simultaneously. Each rat was then given acetaminophen. The pharmacokinetic parameters of acetaminophen of the two groups were significantly different. In the In-Chen-How pretreated group, the maximum concentration of acetaminophen and the area under the plasma concentration-time curve were reduced about 58.4%, 56.7% and 55.4%. To further explain the results, liver microsomal suspensions were obtained from rats that were randomly divided into control and In-Chen-How pretreated group. The levels of CYP1A2 and CYP2E1 in hepatic microsomal protein from pretreated group were increased as compared to that from the control group. It indicated that In-Chen-How can stimulate the activity of CYP isozymes. The changes in the pharmacokinetics of acetaminophen resulting from the administration of In-Chen-How are related to an increase in metabolic activity of CYP1A2 and CYP2E1.

摘要

本研究旨在评估茵陈蒿对大鼠体内对乙酰氨基酚药代动力学及肝微粒体细胞色素P450酶活性的相互作用。将大鼠分为未给予茵陈蒿的对照组(n = 8)和连续5天给予茵陈蒿(按体重约1.0 mL x kg(-1))的预处理组(n = 8)。对照组大鼠同时给予水。然后给每只大鼠服用对乙酰氨基酚。两组对乙酰氨基酚的药代动力学参数有显著差异。在茵陈蒿预处理组中,对乙酰氨基酚的最大浓度和血浆浓度-时间曲线下面积分别降低了约58.4%、56.7%和55.4%。为进一步解释结果,从随机分为对照组和茵陈蒿预处理组的大鼠中获取肝微粒体悬液。与对照组相比,预处理组肝微粒体蛋白中CYP1A2和CYP2E1的水平升高。这表明茵陈蒿可刺激CYP同工酶的活性。茵陈蒿给药导致的对乙酰氨基酚药代动力学变化与CYP1A2和CYP2E1代谢活性增加有关。

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