METABOLISM OF OLTIPRAZ AND GLUTATHIONE-REDUCTASE INHIBITION

被引:23
作者
MOREAU, N
MARTENS, T
FLEURY, MB
LEROY, JP
机构
[1] RHONE POULENC SANTE,CTR RECH VITRY,F-94407 VITRY,FRANCE
[2] FAC PHARM PARIS,CHIM ANALYT LAB,F-75270 PARIS 06,FRANCE
关键词
D O I
10.1016/0006-2952(90)90396-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A decrease in glutathione reductase (GR) activity was observed in Schistosoma mansoni isolated from oltipraz(OPZ)-treated mice. Yeast and Schistosoma mansoni GR-activity was inhibited by OPZ derivatives only. These OPZ-derivatives showed in vitro schistosomicidal activity. Using yeast GR and dithiolium salts of OPZ, time-dependent inactivation and gel chromatography experiments revealed irreversible inhibition dependent on the redox state of the enzyme. Binding of radiolabelled ([3H]7-methyl-8-methylthio-pyrrolo[1,2-a]pyrazine disulphide 1b) obtained from OPZ was observed using exclusion chromatography and equilibrium dialysis. These results indicate that GR can be considered as the target of schistosomicidal activity of OPZ. The lack of inhibitory activity of OPZ and dithiole-thione analogues, and the potent activity of the corresponding pyrrolo-pyrazine derivatives, is consistent with the hypothesis that OPZ is a pro-drug. © 1990.
引用
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页码:1299 / 1305
页数:7
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