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生姜水乙醇提取物对细胞色素P450酶介导的药物代谢的影响。

Effects of an aqueous-ethanolic extract of ginger on cytochrome P450 enzyme-mediated drug metabolism.

作者信息

Kim I S, Kim S Y, Yoo H H

机构信息

College of Pharmacy, Hanyang University, Ansan, Republic of Korea.

出版信息

Pharmazie. 2012 Dec;67(12):1007-9.

Abstract

Ginger has been extensively used as a herbal medicine for thousands of years in Asia; it has also been used as a seasoning agent in several foods and beverages worldwide. In this study, the effect of an aqueous-ethanolic extract of ginger on CYP450-mediated drug metabolism was investigated in vitro to elucidate the herb-drug interactions. A CYP450-specific substrates mixture was incubated with an aqueous-ethanolic extract of ginger in human liver microsomes fortified with an NADPH-generating system, and the metabolites generated from each of the CYP450-specific metabolic reactions were measured by liquid chromatography-tandem mass spectrometry. The ginger extracts were tested at concentrations of 0.05-5 microg/mL. The resulting data showed that the ginger extract inhibited CYP2C19-mediated drug metabolism in a concentration-dependent manner with an IC50 value of 3.8 microg/mL. When the ginger extract was pre-incubated and assessed, the inhibition pattern did not change, indicating that the inhibition of CYP2C19 was competitive rather than mechanism-based. The effects on other CYP isozyme activity were negligible at the concentrations tested. In conclusion, this inhibitory effect of ginger extract could affect the pharmacokinetics and lead to interactions with drugs that are metabolized by CYP2C19.

摘要

数千年来,生姜在亚洲被广泛用作草药;在全球范围内,它还被用作多种食品和饮料的调味剂。在本研究中,体外研究了生姜水乙醇提取物对细胞色素P450(CYP450)介导的药物代谢的影响,以阐明草药-药物相互作用。将CYP450特异性底物混合物与生姜水乙醇提取物在添加了烟酰胺腺嘌呤二核苷酸磷酸(NADPH)生成系统的人肝微粒体中孵育,通过液相色谱-串联质谱法测定每种CYP450特异性代谢反应产生的代谢产物。生姜提取物的测试浓度为0.05 - 5微克/毫升。所得数据表明,生姜提取物以浓度依赖的方式抑制CYP2C19介导的药物代谢,半数抑制浓度(IC50)值为3.8微克/毫升。当对生姜提取物进行预孵育并评估时,抑制模式没有改变,表明对CYP2C19的抑制是竞争性的,而非基于机制的。在所测试的浓度下,对其他CYP同工酶活性的影响可忽略不计。总之,生姜提取物的这种抑制作用可能会影响药代动力学,并导致与经CYP2C19代谢的药物发生相互作用。

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