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首页> 外文期刊>Drug metabolism and pharmacokinetics. >Induction of hepatic cytochrome P450s by the herbal medicine Sophora flavescens extract in rats: impact on the elimination of theophylline.
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Induction of hepatic cytochrome P450s by the herbal medicine Sophora flavescens extract in rats: impact on the elimination of theophylline.

机译:中药苦参提取物诱导大鼠肝细胞色素P450s:对茶碱消除的影响。

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The roots of Sophora flavescens (Sf) have been widely used as a herbal medicine for the treatment of diarrhea, gastrointestinal hemorrhage, and eczema. Cytochrome P450 (P450) forms including CYP1A2, CYP2B, CYP2E1, and CYP3A participate in the oxidative metabolism of theophylline, which is an important bronchodilation agent with a narrow therapeutic index. To assess the interaction of Sf with theophylline, the effects of Sf extract on theophylline-metabolizing P450s and on the pharmacokinetic profile of theophylline were investigated in male Sprague-Dawley rats. Oral treatment of rats with the Sf extract caused dose-dependent increases of liver microsomal oxidation activities toward 7-ethoxyresorufin, 7-pentoxyresorufin, and nifedipine. However, nitrosodimethylamine N-demethylation activity was not affected. The ingestion of Sf extract stimulated theophylline 8-oxidation and N-demethylation activities. The increases of oxidative activities were in consensus with the elevation of the protein levels of CYP1A2, CYP2B1/2, CYP2C11, and CYP3A. Sf-treatment increased the clearance of theophylline and decreased the area under the concentration-time curve (AUC) and the area under the moment curve (AUMC). These results demonstrate that Sf reduces blood theophylline concentration through facilitating the elimination of theophylline. In patients taking Sf, possible P450 induction-induced drug interaction should be noted to decrease the risk of therapeutic failure or adverse effects resulting from the use of additional therapeutic agents.
机译:苦参的根已被广泛用作治疗腹泻,胃肠道出血和湿疹的草药。细胞色素P450(P450)形式包括CYP1A2,CYP2B,CYP2E1和CYP3A参与茶碱的氧化代谢,这是一种重要的支气管扩张剂,具有狭窄的治疗指数。为了评估Sf与茶碱的相互作用,在Sprague-Dawley雄性大鼠中研究了Sf提取物对代谢茶碱的P450和茶碱药代动力学的影响。用Sf提取物对大鼠进行口服治疗会导致肝脏微粒体对7-乙氧基间苯二酚,7-戊氧基间苯二酚和硝苯地平的氧化活性呈剂量依赖性增加。但是,亚硝基二甲胺N-脱甲基活性没有受到影响。摄入Sf提取物可刺激茶碱8氧化和N-去甲基化活性。氧化活性的增加与CYP1A2,CYP2B1 / 2,CYP2C11和CYP3A的蛋白质水平升高一致。 Sf处理可增加茶碱的清除率,并减小浓度-时间曲线(AUC)下的面积和力矩曲线下的面积(AUMC)。这些结果表明,Sf通过促进消除茶碱来降低血液茶碱浓度。在服用Sf的患者中,应注意可能的P450诱导诱导的药物相互作用,以降低因使用其他治疗药物而导致治疗失败或不良反应的风险。

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