Effect of 22 CYP2D6 variants found in the Chinese population on tolterodine metabolism in vitro

被引:0
作者
Wang, Hao [1 ]
Dai, Da-Peng [2 ,3 ]
Sun, Peng [1 ]
Xu, Li-Ping [1 ]
Liang, Bing-Qing [1 ]
Cai, Jian-Ping [2 ,3 ]
Hu, Guo-Xin [1 ]
机构
[1] Wenzhou Med Univ, Sch Pharm, Dept Pharmacol, Wenzhou 325035, Zhejiang, Peoples R China
[2] Beijing Hosp, Key Lab Geriatr, Beijing 100730, Peoples R China
[3] Minist Hlth, Beijing Inst Geriatr, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
CYP2D6; Allelic variants; Tolterodine; Drug metabolism; In vitro; HUMAN CYTOCHROME-P450 2D6; FUNCTIONAL-CHARACTERIZATION; GENETIC POLYMORPHISMS; CLINICAL-SIGNIFICANCE; MOLECULAR-GENETICS; CATALYTIC ACTIVITY; ALLELIC ISOFORMS; DRUG DEVELOPMENT; HAN POPULATION; PHARMACOGENOMICS;
D O I
10.1016/j.cbi.2017.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytochrome P450 2D6 (CYP2D6) is an important member of the cytochrome P450 enzyme superfamily. We recently identified 22 novel variants in the Chinese population using PCR and bidirectional sequencing methods. The aim of this study is to characterize the enzymatic activity of these variants and their effects on the metabolism of the antimuscarinic drug tolterodine in vitro. A baculovirus-mediated expression system was used to express wild-type CYP2D6 and 24 variants (CYP2D6*2, CYP2D6*10, and 22 novel CYP2D6 variants) at high levels. The insect microsomes expressing CYP2D6 proteins were incubated with 0.1-50 mu M tolterodine at 37 degrees C for 30 min and the metabolites were analyzed by high-performance liquid chromatography tandem mass spectrometry system. Of the 24 CYP2D6 variants tested, 2 variants (CYP2D6*92 and CYP2D6*96) were found to be catalytically inactive, 4 variants (CYP2D6*94, F164L, F219S and D336N) exhibited markedly increased intrinsic clearance values (V-max/K-m) compared with the wild-type (from 6634 to 99.79%), whereas 4 variants (CYP2D6*10, *93, *95 and E215K) exhibited significantly decreased values (from 49.02 to 98.50%). This is the first report of all these rare alleles for tolterodine metabolism and these findings suggest that more attention should be paid to subjects carrying these infrequent CYP2D6 alleles when administering tolterodine in the clinic. (C) 2017 Published by Elsevier Ireland Ltd.
引用
收藏
页码:10 / 15
页数:6
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