Cermak Rainer, Wolffram Siegfried
Institute of Veterinary Physiology, An den Tierkliniken 7, University of Leipzig, D-04103 Leipzig, Germany.
Curr Drug Metab. 2006 Oct;7(7):729-44. doi: 10.2174/138920006778520570.
In recent years, public and scientific interest in plant flavonoids has tremendously increased due to postulated health benefits. Whereas the amount of flavonoids ingested with the regular diet is rather low, the use of supplements enriched with these polyphenolics is becoming increasingly popular. This raises concerns about possible interactions of flavonoids with therapeutic drugs, because both are xenobiotics and, thus, share at least partially the same metabolic pathways. A number of in vitro studies have shown effects of flavonoids on enzymes involved in xenobiotic metabolism, like cytochrome P450 monooxygenases and phase II conjugation enzymes, or on membrane transporters involved in drug excretion. Several investigations have also reported changes of drug bioavailability by certain flavonoids. This article attempts to present an overview of flavonoid effects on pathways involved in drug metabolism. It focuses on phase I and phase II enzymes as well as on transporters involved in drug metabolism which are expressed in the gastrointestinal tract.
近年来,由于假定的健康益处,公众和科学界对植物黄酮类化合物的兴趣大幅增加。虽然通过常规饮食摄入的黄酮类化合物数量相当少,但富含这些多酚类物质的补充剂的使用却越来越普遍。这引发了人们对黄酮类化合物与治疗药物可能相互作用的担忧,因为两者都是外源性物质,因此至少部分共享相同的代谢途径。一些体外研究表明,黄酮类化合物对参与外源性物质代谢的酶(如细胞色素P450单加氧酶和II相结合酶)或参与药物排泄的膜转运蛋白有影响。几项研究还报告了某些黄酮类化合物会改变药物的生物利用度。本文试图概述黄酮类化合物对药物代谢相关途径的影响。它重点关注I相和II相酶以及在胃肠道中表达的参与药物代谢的转运蛋白。