Department of Pharmacology, Toxicology & Therapeutics, University of Kansas Medical Center, Kansas City, KS, USA.
Center for Computational Toxicology and Exposure, US EPA, Durham, NC, USA.
Xenobiotica. 2021 Mar;51(3):279-286. doi: 10.1080/00498254.2020.1867929. Epub 2020 Dec 28.
Individual differences in cytochrome P450 (CYP) enzymes contribute to responses to drugs and environmental chemicals. The expression of CYPs is influenced by sex, age, and ethnicity. Human CYP studies are often conducted with human liver microsomes and liver cells to evaluate chemical induction and drug interactions. However, the basal or constitutive expression of CYP transcripts and enzyme activities in the intact liver are also important in our understanding of individual variation in CYPs. This study utilised 100 human liver samples to profile the constitutive expression of CYP1A2, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1, 3A4, and 4A11 enzyme activity and transcript levels. The mRNA expression of the CYPs and xenobiotic receptors , , and was examined qPCR. Results showed that there was greater inter-individual variation in mRNA expression than in enzyme activities, except for CYP2C19. Females had higher CYP3A4 activity than males. Children had lower CYP4A14 activity, while elderly had lower P450 oxidoreductase activity. Compared to Caucasians, Hispanics had higher CYP2C8 activity and higher , , and mRNA expression, whereas African Americans had lower CYP2D6 mRNA expression. These results add to our understanding of individual variations in xenobiotic metabolism and toxicology.
个体差异的细胞色素 P450(CYP)酶对药物和环境化学物质的反应有影响。CYP 的表达受性别、年龄和种族的影响。CYP 的人类研究通常使用人肝微粒体和肝细胞进行,以评估化学诱导和药物相互作用。然而,完整肝脏中 CYP 转录本和酶活性的基础或组成型表达对于我们理解 CYP 的个体差异也很重要。本研究利用 100 个人肝样本对 CYP1A2、2B6、2C8、2C9、2C19、2D6、2E1、3A4 和 4A11 酶活性和转录水平的组成型表达进行了分析。使用 qPCR 检测了 CYP 和外源性受体的 mRNA 表达。结果表明,mRNA 表达的个体间差异大于酶活性,除了 CYP2C19。女性的 CYP3A4 活性高于男性。儿童 CYP4A14 活性较低,而老年人 P450 氧化还原酶活性较低。与白种人相比,西班牙裔人 CYP2C8 活性较高, 、 、 mRNA 表达较高,而非洲裔美国人 CYP2D6 mRNA 表达较低。这些结果增加了我们对异生物代谢和毒理学个体差异的理解。