http://jcps.bjmu.edu.cn

• 研究论文 • 上一篇    下一篇

中国壮族志愿者S-美芬妥英和异喹胍羟化代谢多态性研究

匡唐永, 罗其葵, 张家美, 邹安庆, 楼雅卿   

  1. 1. 北京医科大学基础医学院药理学系, 北京 100083;
    2. 北京医科大学天然药物及仿生药物国家重点实验室, 北京医科大学, 北京 100083
  • 收稿日期:1993-12-22 修回日期:1994-03-29 出版日期:1995-06-15 发布日期:1995-06-15

Hydroxylation Polymorphisms of S-mephenytoin and Debrisoquin in Native Normal Chinese Zhuang Minority Volunteers

Tang-Yong Kuang, Qi-kui Luo, Jia-Mei Zhang, An-Qing Zou, Ya-Qing Lou   

  1. 1. Department of pharmacology; School of Basic Medical Sciences Beijing Medecal University; Beijing 100083;
    2. National Laboratory of Natural and Biomimtic Drugs; Beijing Medecal University; Beijing 100083
  • Received:1993-12-22 Revised:1994-03-29 Online:1995-06-15 Published:1995-06-15

摘要: 118名中国壮族(广西壮族自治区)志愿者一次口服消旋美芬妥英100 mg和异喹胍10 mg, 应用气相色谱法分别测定尿中S-R-美芬妥英含量比值和异喹胍及其代谢物4羟异喹胍含量比值, 作为体内药物羟化代谢能力的指标。实验结果表明, 118名志愿者中有12名的S/R美芬妥英比值大于1.0, 是为S-美芬妥英弱羟化代谢者。说明我国壮族人群中S-美芬妥英羟化代谢缺陷频发率高达10.2%。但在118名壮族志愿者中未发现异喹胍弱羟化代谢者, S-美芬妥英的羟化代谢多态性和异喹胍羟化代谢多态性不存在着相关性。另外, 选择其中16名志愿者(4名弱代谢者, 12名强代谢者)研究了尿中美芬妥英和异喹胍及其代谢物的消除动力学规律。并估算了它们主要的药代动力学参数。

关键词: 美芬妥英, 异喹胍, 羟化代谢遗传多态性, 药代动力学, 中国人群, 气相色谱法

Abstract: S-mephenytoin and debrisoquin hydroxylation abilities were investigated in 118 normal Chinese Zhuang minority volunteers after co-administration po 100 mg racemic mephenytoin(MP)and 10 mg debrisoquin (DB). The ratio between S-and R-enantiomers of mephenytoin in urinewas determined by implication of GC-NPD and used as the measure of the drug hydroxylation. 2 ofthe 118 subjects had S/R ratios greater than 1.0 and were poor hydroxylators of S- mephenytoin. The frequency of S-mephenytoin poor metabolizers (PM) was 10.2%. No PM of debrisoquin was found in the volunteers. It indicated that there was no relationship between S-mephenytoin P(4')-hydroxylation and debrisoquin 4-hydroxylation polymorphisms in Chinese Zhuang Minority population. In addition, 16 of the 118 volunteers(4 PMs and 12 EMs of S-mephenytoin) were se-lected to conduct the elimination kinetic studies of racemic mephenytoin and debrisoquin in urine. The pharmacokinetic parameters of S-, R- mephenytoin, DB and 4-OH-DB were calculated.

Key words: Mephenytoin, Debrisoquin, Hydroxylation, Inheritic polymorphism, Pharmacokinetics, Gas chromatography

Supporting: