乌竹玉汤及其成分对药物代谢酶的影响。

Y. Ueng, M. Don, Hsiao-Chi Peng, Shu-Yun Wang, Jong-Jing Wang, Chieh‐fu Chen
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引用次数: 31

摘要

复方草药乌竹郁汤用于治疗偏头痛和感冒引起的呕吐。为了研究中药与药物代谢的相互作用,我们研究了乌初愈汤对C57BL/6J小鼠肝脏和肾脏细胞色素P450 (CYP)、udp -葡萄糖醛基转移酶(UGT)和谷胱甘肽s -转移酶(GST)的影响。每天给药5 g/kg的乌初玉汤3 d后,小鼠肝微粒体7-乙氧基间甲酚o -去甲基化(EROD)和7-甲氧基间甲酚o -去甲基化活性分别增加2.5倍和2.9倍。然而,CYP对7-乙氧基香豆素、苯非他明、n -亚硝基二甲胺、红霉素和硝苯地平的活性以及UGT和GST的偶联活性不受影响。在肾脏中,乌竹玉汤处理对Cyp、UGT和GST活性无影响。乌乌玉汤四种成分中,只有乌乌玉提取物能提高EROD活性和CYP1a2蛋白水平。山茱萸中主要活性生物碱为车茱萸碱、evolodiamine和脱氢evolodiamine。在乌竹玉汤中相应剂量下,芦地胡卡平处理提高了肝脏EROD活性,而evolodiamine和脱氢evolodiamine则没有作用。这些结果表明,摄入乌竹玉汤可提高小鼠肝脏Cyp1a2活性和蛋白水平。乌竹玉汤对CYP1a2的诱导至少有部分作用。患者应注意乌竹玉汤与CYP1A2底物的药物相互作用。
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Effects of Wu-chu-yu-tang and its component herbs on drug-metabolizing enzymes.
The compound herbal medicine Wu-chu-yu-tang is used for the treatment of migraine and vomiting accompanying a cold. To assess the interactions of herb and drug metabolism, effects of Wu-chu-yu-tang on hepatic and renal cytochrome P450 (CYP), UDP-glucuronosyl transferase (UGT) and glutathione S-transferase (GST) were studied in C57BL/6J mice. Treatment of mice with 5 g/kg per day Wu-chu-yu-tang for 3 days caused 2.5-fold and 2.9-fold increases of liver microsomal 7-ethoxyresorufin O-deethylation (EROD) and 7-methoxyresorufin O-demethylation activities, respectively. However, CYP activities toward 7-ethoxycoumarin, benzphetamine, N-nitrosodimethylamine, erythromycin and nifedipine, and conjugation activities of UGT and GST were not affected. In kidney, Wu-chu-yu-tang-treatment had no effects on Cyp, UGT and GST activities. Among the four component herbs of Wu-chu-yu-tang, only Evodiae Fructus (Wu-chu-yu) extract increased EROD activity and CYP1a2 protein level. In E. Fructus, rutaecarpine, evodiamine and dehydroevodiamine are the main active alkaloids. At the doses corresponding to their contents in Wu-chu-yu-tang, rutaecarpine-treatment increased hepatic EROD activity, whereas evodiamine and dehydroevodiamine had no effects. These results demonstrated that ingestion of Wu-chu-yu-tang elevated mouse hepatic Cyp1a2 activity and protein level. E. Fructus and rutaecarpine contributed at least in part to the CYP1a2 induction by Wu-chu-yu-tang. Patients should be cautioned about the drug interaction of Wu-chu-yu-tang and CYP1A2 substrates.
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