Strolin Benedetti M
UCB Pharma SA, 420, rue d'Estienne-d'Orves, 92705 Colombes, France.
Ann Pharm Fr. 2011 Jan;69(1):45-52. doi: 10.1016/j.pharma.2010.10.004. Epub 2010 Dec 28.
Although the majority of oxidative metabolic reactions are mediated by the CYP superfamily of enzymes, non-CYP-mediated oxidative reactions can play an important role in the metabolism of xenobiotics. Among the major oxidative enzymes, other than CYPs, involved in the oxidative metabolism of drugs and other xenobiotics, the flavin-containing monooxygenases (FMOs), the molybdenum hydroxylases [aldehyde oxidase (AO) and xanthine oxidase (XO)] and the FAD-dependent amine oxidases [monoamine oxidases (MAOs) and polyamine oxidases (PAOs)] are discussed in this minireview. In a similar manner to CYPs, these oxidative enzymes can also produce therapeutically active metabolites and reactive/toxic metabolites, modulate the efficacy of therapeutically active drugs or contribute to detoxification. Many of them have been shown to be important in endobiotic metabolism (e.g. XO, MAOs), and, consequently, interactions between drugs and endogenous compounds might occur when they are involved in drug metabolism. In general, most non-CYP oxidative enzymes (e.g. FMOs, MAOs) appear to be noninducible or much less inducible than the CYP system. Some of these oxidative enzymes exhibit polymorphic expression, as do some CYPs (e.g. FMO3). It is possible that the contribution of non-CYP oxidative enzymes to the overall metabolism of xenobiotics is underestimated, as most investigations of drug metabolism have been performed using experimental conditions optimised for CYP activity, although in some cases the involvement of non-CYP oxidative enzymes in xenobiotic metabolism has been inferred from not sufficient experimental evidence.
虽然大多数氧化代谢反应是由细胞色素P450(CYP)超家族酶介导的,但非CYP介导的氧化反应在外源生物代谢中也可发挥重要作用。在参与药物和其他外源生物氧化代谢的主要氧化酶中,除CYP外,本文综述还讨论了含黄素单加氧酶(FMO)、钼羟化酶[醛氧化酶(AO)和黄嘌呤氧化酶(XO)]以及黄素腺嘌呤二核苷酸(FAD)依赖性胺氧化酶[单胺氧化酶(MAO)和多胺氧化酶(PAO)]。与CYP类似,这些氧化酶也可产生治疗活性代谢物和反应性/毒性代谢物,调节治疗活性药物的疗效或促进解毒。其中许多酶已被证明在内源生物代谢中很重要(如XO、MAO),因此,当它们参与药物代谢时,药物与内源性化合物之间可能会发生相互作用。一般来说,大多数非CYP氧化酶(如FMO、MAO)似乎不可诱导或诱导性远低于CYP系统。其中一些氧化酶表现出多态性表达,一些CYP也是如此(如FMO3)。非CYP氧化酶对外源生物整体代谢的贡献可能被低估了,因为大多数药物代谢研究都是在针对CYP活性优化的实验条件下进行的,尽管在某些情况下,非CYP氧化酶参与外源生物代谢是根据不足的实验证据推断出来的。