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Isolation analysis and in vitro assessment of CYP3A4 inhibition by methylxanthines extracted from Pu-erh and Bancha tea leaves

机译:普-茶和板茶茶中提取的甲基黄嘌呤对CYP3A4抑制作用的分离分析和体外评价

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摘要

Methylxanthines, purine alkaloids found in plants, are found in beverages (coffee, tea, cocoa) and foods (chocolate and other cocoa-containing foods) commonly consumed worldwide. Members of this family include caffeine, theophylline and theobromine. Methylxanthines have a variety of pharmacological effects, and caffeine and theophylline are used as pharmaceuticals. Methylxanthines are metabolized in the liver predominantly by the enzyme CYP1A2. Their co-administration with CYP1A2 inhibitors may lead to pharmacokinetic interactions. Little is known about the possible drug interactions between caffeine and substrates of other CYP450 enzymes. In our study, methylxanthine fractions inhibited CYP3A4 in a concentration-dependent manner. Concomitant consumption of green tea with CYP3A4 substrates could increase the possibility of interactions, and this requires further clarification. The inhibition of CYP3A4 is not only due to the presence of catechin derivatives but methylxanthines may also contribute to this effect.
机译:甲基黄嘌呤是植物中发现的嘌呤生物碱,存在于全世界普遍消费的饮料(咖啡,茶,可可粉)和食品(巧克力和其他含可可粉的食品)中。这个家庭的成员包括咖啡因,茶碱和可可碱。甲基黄嘌呤具有多种药理作用,咖啡因和茶碱被用作药物。甲基黄嘌呤主要在肝脏中被CYP1A2酶代谢。它们与CYP1A2抑制剂的共同给药可能导致药代动力学相互作用。关于咖啡因和其他CYP450酶底物之间可能的药物相互作用的了解甚少。在我们的研究中,甲基黄嘌呤部分以浓度依赖的方式抑制CYP3A4。绿茶与CYP3A4底物的并用可能会增加相互作用的可能性,这需要进一步澄清。 CYP3A4的抑制不仅是由于儿茶素衍生物的存在,而且甲基黄嘌呤也可能导致这种作用。

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