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双重基因多态性对磺胺二甲嘧啶反应的影响。

Influence of double genetic polymorphism on response to sulfamethazine.

作者信息

Woolhouse N M, Atu-Taylor L C

出版信息

Clin Pharmacol Ther. 1982 Mar;31(3):377-83. doi: 10.1038/clpt.1982.48.

Abstract

Combined effects of a double genetic polymorphism on sulfamethazine-induced changes in erythrocyte-reduced glutathione (GSH) concentration were investigated in 16 healthy Ghanaian men. The subjects were divided into four subgroups on the basis of their glucose-6-phosphate dehydrogenase (G-6-PD) activity levels and acetylator phenotypes. Each received a single oral dose of sulfamethazine (1.5 gm). Erythrocyte concentration of GSH and plasma concentrations of drug were determined in samples taken at specific times after dosing. Sulfamethazine treatment induced a decrease in erythrocyte GSH concentration in all subjects. The degree of exposure to sulfamethazine was greater in slow acetylators, as evidenced by higher plasma concentrations, longer half-lifes, and greater area under the plasma concentration-time curves. The greatest decrease in GSH concentration occurred in subjects who where both G-6-PD deficient and phenotypically slow acetylators. In these subjects the effect of the double genetic defect was approximately additive. Drug-induced hemolysis is associated with a low erythrocyte GSH concentration. Our data suggest that slow acetylator status is likely to increase susceptibility to hemolysis in G-6-PD-deficient individuals exposed to potentially hemolytic arylamines.

摘要

在16名健康的加纳男性中研究了双重基因多态性对磺胺二甲嘧啶诱导的红细胞还原型谷胱甘肽(GSH)浓度变化的联合影响。根据葡萄糖-6-磷酸脱氢酶(G-6-PD)活性水平和乙酰化表型将受试者分为四个亚组。每组均接受单次口服磺胺二甲嘧啶(1.5克)。在给药后特定时间采集的样本中测定红细胞GSH浓度和血浆药物浓度。磺胺二甲嘧啶治疗导致所有受试者的红细胞GSH浓度降低。慢乙酰化者对磺胺二甲嘧啶的暴露程度更高,这表现为血浆浓度更高、半衰期更长以及血浆浓度-时间曲线下面积更大。GSH浓度下降最大的情况发生在G-6-PD缺乏且表型为慢乙酰化者的受试者中。在这些受试者中,双重基因缺陷的影响大致是相加的。药物诱导的溶血与红细胞GSH浓度低有关。我们的数据表明,慢乙酰化状态可能会增加G-6-PD缺乏个体在接触潜在溶血芳胺时发生溶血的易感性。

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