首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Traditional Chinese Medicines Wu Wei Zi (Schisandra chinensis Baill) and Gan Cao (Glycyrrhiza uralensis Fisch) Activate Pregnane X Receptor and Increase Warfarin Clearance in Rats
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Traditional Chinese Medicines Wu Wei Zi (Schisandra chinensis Baill) and Gan Cao (Glycyrrhiza uralensis Fisch) Activate Pregnane X Receptor and Increase Warfarin Clearance in Rats

机译:中药五味子(五味子)和甘草(甘草)可激活孕烷X受体并增加大鼠的华法林清除率

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The traditional Chinese medicines (TCMs) are essential components of alternative medicines.Many TCMs are known to alter the expression of hepatic drug-metabolizing enzymes and transporters.The molecular mechanism by which TCMs and/or their constituents regulate enzyme and transporter expression,however,has remained largely unknown.In this report,we show that two TCMs,Wu Wei Zi (Schisandra chinensis Baill) and Gan Cao (Glycyrrhiza uralensis Fisch),and their selected constituents activate the xenobiotic orphan nuclear receptor pregnane X receptor (PXR).Treatment with TCM extracts and the Schisandrol and Schisandrin constituents of Wu Wei Zi induced the expression of drug-metabolizing enzymes and transporters in reporter gene assays and in primary hepatocyte cultures.The affected enzymes and transporters include CYP3A and 2C isozymes and the multidrug resistance-associated protein 2.In transient transfection and reporter gene assays,the Schisandrin constituents of Wu Wei Zi had an estimated EC_(50) of 2 and 1.25 muM on hPXR and mPXR,respectively.Interestingly,mutations that were intended to alter the pore of the ligand-binding cavity of PXR had species-specific effects on the activities of the individual Schisandrols and Schisandrins.In rats,the administration of Wu Wei Zi and Gan Cao increased the metabolism of the coadministered warfarin,reinforcing concerns involving the safe use of herbal medicines and other nutraceuticals to avoid PXR-mediated drug-drug interactions.Meanwhile,the activation of PXR and induction of detoxifying enzymes provide a molecular mechanism for the hepatoprotective effects of certain TCMs.
机译:中药(TCMs)是替代药物的基本组成部分。已知许多中药会改变肝药物代谢酶和转运蛋白的表达。中药和/或其成分调节酶和转运蛋白表达的分子机制,在此报告中,我们显示了五味子(五味子)和甘草(甘草)两个中药,它们的选定成分激活了异源生物孤儿核受体孕烷X受体(PXR)。用中药提取物和五味子的五味子醇和五味子醇成分诱导药物代谢酶和转运蛋白在报告基因试验和原代肝细胞培养中的表达,受影响的酶和转运蛋白包括CYP3A和2C同工酶以及与多药耐药相关的蛋白2.在瞬时转染和报告基因检测中,五味子的五味子成分具有感觉分别对hPXR和mPXR的EC_(50)为2和1.25μM。有趣的是,旨在改变PXR配体结合腔孔的突变对各个五味子和五味子的活性具有物种特异性的影响。在大鼠中,五味子和甘草的给药增加了并用华法林的代谢,从而增加了涉及安全使用草药和其他营养品以避免PXR介导的药物相互作用的担忧。同时,PXR的活化和诱导排毒酶的提供为某些中药的保肝作用提供了分子机制。

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