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CYP2C19基因多态性对中国人体内兰索拉唑药代动力学及其5-羟基代谢通路的影响

严非 夏春华 熊玉卿

中国临床药理学与治疗学2011,Vol.16Issue(12):1397-1402,6.
中国临床药理学与治疗学2011,Vol.16Issue(12):1397-1402,6.

CYP2C19基因多态性对中国人体内兰索拉唑药代动力学及其5-羟基代谢通路的影响

Effect of CYP2C19 genetic polymorphism on pharmacokinetic characterstics and 5-hydroxyl metabolic pathway of lansoprazole in Chinese volunteers

严非 1夏春华 1熊玉卿1

作者信息

  • 1. 南昌大学医学院临床药理研究所,南昌330006,江西
  • 折叠

摘要

Abstract

AIM: To investigate the effect of CYP2C19 polymorphism on pharmacokinetic characteristics and 5-hydroxyl metabolic pathway of lansoprazole in Chinese subjects. METH-ODS: Twelve healthy subjects were typed by u-sing RFLP-PCR method. After intravenous drip 30 mg lansoprazole, the plasma concentrations of lansoprazole in subjects were determined byLC-MS method. The pharmacokinetic parameters of lansoprazole and AUClpz/AUC5-Ohlpz were calculated and compared between different groups. RESULTS-. After all the subjects were given 30 mg lansoprazole, it found that the AUCo-,, AUCo-(x), CLz, ( AUCLpz/ AUC5-oh)0-t, and (AUCLpZ/AUC5-oh)0-∞ of the mutant types were equivalent to 2.381, 2.572, 0. 428, 3. 602 and 4. 083-fold as those of the wild types, respectively. CONCLUSION: The CYP2C19 genetic polymorphism, which has significant influence on the pharmacokinetic characteristics of the lansoprazole in Chinese volun-teers (P<0. 05), has very significant influence on the 5-hydroxyl metabolic pathway of the lansoprazole (P<0. 01). The result suggests that CYP2C19 genetic polymorphism is one of the important factors leading to individual concentration differences of the lansoprazole and has a better relevance with the 5-hydroxyl metabolic pathway.

关键词

CYP2C19/基因多态性/兰索拉唑/药代动力学

Key words

CYP2C19/Polymorphism,Lansoprazole/Pharmacokinetics

分类

医药卫生

引用本文复制引用

严非,夏春华,熊玉卿..CYP2C19基因多态性对中国人体内兰索拉唑药代动力学及其5-羟基代谢通路的影响[J].中国临床药理学与治疗学,2011,16(12):1397-1402,6.

基金项目

国家十一五科技重大专项(2009ZX09309-003-02) (2009ZX09309-003-02)

国家十二五科技重大专项(2011ZX09302-007-03) (2011ZX09302-007-03)

中国临床药理学与治疗学

OACSCDCSTPCD

1009-2501

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