Impact of CYP2C9 Polymorphism Found in the Chinese Population on the Metabolism of Propofol in Vitro

被引:16
|
作者
Lian, Qing-Quan [1 ]
Pan, Pei-Pei [2 ]
Li, Jun-Wei [2 ]
Lin, Han [1 ]
Hu, Guo-Xin [2 ]
Zuo, Ming-Zhang [3 ]
Cai, Jian-Ping [4 ,5 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Anesthesiol, Wenzhou 325035, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Sch Pharm, Wenzhou 325035, Zhejiang, Peoples R China
[3] Beijing Hosp, Dept Anesthesia, Minist Hlth, Beijing 100730, Peoples R China
[4] Beijing Hosp, Key Lab Geriatr, Beijing 100730, Peoples R China
[5] Minist Hlth, Beijing Inst Geriatr, Beijing 100730, Peoples R China
基金
美国国家科学基金会;
关键词
propofol; microsome; metabolism; CYP2C9; allelic variant; catalytic character; CYTOCHROME P4502C9; LIVER-MICROSOMES; PHARMACOKINETICS; HYDROXYLATION; LORNOXICAM; VARIANTS; RAT; DOG;
D O I
10.1248/bpb.b14-00671
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The microsomal CYP2C9 alleles involved in the biotransformation of propofol, a widely used anesthetic agent, were investigated in vitro. To examine the enzymatic activity of the CYP2C9 alleles, kinetic parameters for propofol 4-hydroxylation were determined in recombinant human P450s CYP2C9 microsomes from Sf21 insects cells carrying CYP2C9*1 and other variants. Some of the variants showed decreased enzyme activity compared with the wild type, as previously reported. Two variants (CYP2C9*36 and *56) were found substantially to increase intrinsic clearance relative to the wild type variant. Most variants significantly (p<0.05) decreased intrinsic clearance of propofol compared with the wild type, except *11, *47, and *54. This study is the first to report these rare alleles for propofol metabolism, providing fundamental data for further clinical studies on CYP2C9 alleles for propofol metabolism in vivo.
引用
收藏
页码:531 / 535
页数:5
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