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首页> 外文期刊>BioMed research international >Quercetin Significantly Inhibits the Metabolism of Caffeine, a Substrate of Cytochrome P450 1A2 Unrelated to CYP1A2* 1C (-2964G>A) and *1F (734C>A) Gene Polymorphisms
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Quercetin Significantly Inhibits the Metabolism of Caffeine, a Substrate of Cytochrome P450 1A2 Unrelated to CYP1A2* 1C (-2964G>A) and *1F (734C>A) Gene Polymorphisms

机译:槲皮素显着抑制咖啡因的代谢,咖啡因是与CYP1A2 * 1C(-2964G> A)和* 1F(734C> A)基因多态性无关的细胞色素P450 1A2的底物

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Background. Quercetin is abundant in plants and human diets. Previous studies indicated that quercetin inhibited the activity of CYP1A2, and the combination of quercetin with the substrates of CYP1A2 might produce herb-drug interactions. This research aims to determine the effects of quercetin and the CYP1A2 gene polymorphisms, namely, CYP1A2*1C (-2964G>A) and *1F (734C>A), on the metabolism of caffeine. Method. The experiment was designed into two treatment phases separated by a 2-week washout period. Six homozygous individuals for the CYP1A2*1C/ *1F (GG/AA) genotype and 6 heterozygous individuals for the CYP1A2* 1C/ * IF (GA/CA) genotype were enrolled in the study. Quercetin capsules (500 mg) were given to each volunteer once daily for 13 consecutive days, and after that, each subject was coadministrated 100 mg caffeine capsules with 500 mg quercetin on the 14th day. Then a series of venous blood samples were collected for HPLC analysis. Correlation was determined between pharmacokinetics of caffeine and paraxanthine with caffeine metabolite ratio. Results. Quercetin significantly affected the pharmacokinetics of caffeine and its main metabolite paraxanthine, while no differences were found in the pharmacokinetics of caffeine and paraxanthine between GG/AA and GA/CA genotype groups. Conclusion. Quercetin significantly inhibits the caffeine metabolism, which is unrelated to CYP1A2* 1C (-2964G>A) and * 1F (734C>A) gene polymorphisms.
机译:背景。槲皮素在植物和人类饮食中含量丰富。先前的研究表明槲皮素抑制CYP1A2的活性,而槲皮素与CYP1A2的底物结合可能会产生草药-药物相互作用。本研究旨在确定槲皮素和CYP1A2基因多态性CYP1A2 * 1C(-2964G> A)和* 1F(734C> A)对咖啡因代谢的影响。方法。将实验设计为两个治疗阶段,每个阶段需要2周的冲洗时间。 CYP1A2 * 1C / * 1F(GG / AA)基因型的6个纯合子和CYP1A2 * 1C / * IF(GA / CA)基因型的6个杂合子被纳入研究。每个志愿者每天一次连续13天给予槲皮素胶囊(500 mg),然后,在第14天将每位受试者100 mg咖啡因胶囊与500 mg槲皮素共同给药。然后收集一系列静脉血样品进行HPLC分析。确定了咖啡因和对黄嘌呤的药代动力学与咖啡因代谢物比例之间的相关性。结果。槲皮素显着影响咖啡因及其主要代谢产物对黄嘌呤的药代动力学,而在GG / AA和GA / CA基因型组之间,咖啡因和对黄嘌呤的药代动力学没有差异。结论。槲皮素显着抑制咖啡因代谢,这与CYP1A2 * 1C(-2964G> A)和* 1F(734C> A)基因多态性无关。

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