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细胞色素P450氧化还原酶多态性对十种细胞色素P450代谢活性的影响在人肝微粒体中因细胞色素P450基因多态性而有所不同。

Effect of P450 Oxidoreductase Polymorphisms on the Metabolic Activities of Ten Cytochrome P450s Varied by Polymorphic CYP Genotypes in Human Liver Microsomes.

作者信息

Fang Yan, Gao Na, Tian Xin, Zhou Jun, Zhang Hai-Feng, Gao Jie, He Xiao-Pei, Wen Qiang, Jia Lin-Jing, Jin Han, Qiao Hai-Ling

出版信息

Cell Physiol Biochem. 2018;47(4):1604-1616. doi: 10.1159/000490934. Epub 2018 Jun 27.

Abstract

UNLABELLED

Background/ Aims: Little is known about the effect of P450 oxidoreductase (POR) gene polymorphisms on the activities of CYPs with multiple genotypes.

METHODS

We genotyped 102 human livers for 18 known POR single nucleotide polymorphisms (SNPs) with allelic frequencies greater than 1% as well as for 27 known SNPs in 10 CYPs. CYP enzyme activities in microsomes prepared from these livers were determined by measuring probe substrate metabolism by high performance liquid chromatograph.

RESULTS

We found that the effects of the 18 POR SNPs on 10 CYP activities were CYP genotype-dependent. The POR mutations were significantly associated with decreased overall Km for CYP2B6 and 2E1, and specific genotypes within CYP1A2, 2A6, 2B6, 2C8, 2D6 and 2E1 were identified as being affected by these POR SNPs. Notably, the effect of a specific POR mutation on the activity of a CYP genotype could not be predicted from other CYP genotypes of even the same CYP. When combining one POR SNP with other POR SNPs, a hitherto unrecognized effect of multiple-site POR gene polymorphisms (MSGP) on CYP activity was uncovered, which was not necessarily consistent with the effect of either single POR SNP.

CONCLUSIONS

The effects of POR SNPs on CYP activities were not only CYP-dependent, but more importantly, CYP genotype-dependent. Moreover, the effect of a POR SNP alone and in combination with other POR SNPs (MSGP) was not always consistent, nor predictable. Understanding the impact of POR gene polymorphisms on drug metabolism necessitates knowing the complete SNP complement of POR and the genotype of the relevant CYPs.

摘要

未标记

背景/目的:关于细胞色素P450氧化还原酶(POR)基因多态性对具有多种基因型的细胞色素P450(CYPs)活性的影响,人们了解甚少。

方法

我们对102个供体肝脏进行基因分型,检测18个已知的等位基因频率大于1%的POR单核苷酸多态性(SNPs)以及10种CYPs中的27个已知SNPs。通过高效液相色谱法测量探针底物代谢,来确定从这些肝脏制备的微粒体中的CYP酶活性。

结果

我们发现18个POR SNPs对10种CYP活性的影响取决于CYP基因型。POR突变与CYP2B6和2E1的总体米氏常数(Km)降低显著相关,并且确定CYP1A2、2A6、2B6、2C8、2D6和2E1中的特定基因型受这些POR SNPs影响。值得注意的是,即使对于同一CYP的其他CYP基因型,也无法从其预测特定POR突变对某一CYP基因型活性的影响。当将一个POR SNP与其他POR SNPs结合时,发现了多位点POR基因多态性(MSGP)对CYP活性的一种前所未有的影响,这不一定与单个POR SNP的影响一致。

结论

POR SNPs对CYP活性的影响不仅取决于CYP,更重要的是,还取决于CYP基因型。此外,单独的POR SNP及其与其他POR SNPs(MSGP)结合的影响并不总是一致的,也无法预测。了解POR基因多态性对药物代谢的影响需要知道POR的完整SNP互补序列以及相关CYPs的基因型。

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