Clifton G, Kaplowitz N, Wallin J D, Kuhlenkamp J
Biochem J. 1975 Aug;150(2):259-62. doi: 10.1042/bj1500259.
Treatment of male rats with 3,4-benzopyrene, 3-methylcholanthrene and phenobarbital resulted in the induction of glutathione S-aryl- and S-aralkyl-transferase activities in kidney cytosol. Benzopyrene produced 77 and 44% increases in aryl and aralkyl activities respectively. Methylcholanthrene caused 73 and 86% increases in the retrospective activities, whereas phenobarbital treatment increased only aralkyl activity (51%). There was no effect on epoxide or alkyl glutathione S-transferase activities with these treatments. Differences were found between the specific activities of the four glutathione S-transferases in females and males, with the following female/male ratios: aryl 0.74; aralkyl 2.37; epoxide 1.52; alkyl 1.33. No changes in Km values were observed relative to drug induction or sex differences. Comparisons are made between the findings of this report and corresponding experiements with liver.
用3,4-苯并芘、3-甲基胆蒽和苯巴比妥处理雄性大鼠,可诱导肾细胞溶质中谷胱甘肽S-芳基和S-芳烷基转移酶的活性。苯并芘使芳基和芳烷基活性分别增加了77%和44%。甲基胆蒽使这两种活性分别增加了73%和86%,而苯巴比妥处理仅使芳烷基活性增加(51%)。这些处理对环氧化物或烷基谷胱甘肽S-转移酶活性没有影响。在雌性和雄性中发现了四种谷胱甘肽S-转移酶的比活性存在差异,其雌性/雄性比率如下:芳基0.74;芳烷基2.37;环氧化物1.52;烷基1.33。相对于药物诱导或性别差异,未观察到Km值的变化。本报告的研究结果与肝脏的相应实验进行了比较。