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药物诱导雄性和雌性大鼠肝脏谷胱甘肽S-转移酶*

Drug induction of hepatic glutathione S-transferases in male and female rats*.

作者信息

Kaplowitz N, Kuhlekamp J, Clifton G

出版信息

Biochem J. 1975 Feb;146(2):351-6. doi: 10.1042/bj1460351.

Abstract

The induction of the glutathione S-transferases by phenobarbital and polycyclic hydrocarbons was studied in male and female rats. Administration of phenobarbital resulted in 60-80% increase in S-aryl and S-aralkyl enzyme specific activities, whereas the S-epoxide and S-alkyl activities were increased by 30-40%. In following the sequence of induction, the former two activities were noted to reach peak activities before an increase in the latter two activities was observed. Both 3-methylcholanthrene and 3,4-benzopyrene were shown toi nduce these four enzymic activities, although without the discrimination between pairs of activities noted with phenobarbital. No change in Km accompanied the increase in Vmax. after induction by drugs, and no change occurred in Ki for sulphobromophthalein inhibition. Significantly lower enzyme specific activities were found for three of the activities studied in female rats but no difference was observed in the S-alkyltransferase activity. However, the proportional increase in the enzymic activities in response to phenobarbital was the same in males and females. These studies demonstrate the drug induction of a group of cytosolic drug-metabolizing enzymes as well as the identification of sex differences in these activities.

摘要

研究了苯巴比妥和多环烃对雄性和雌性大鼠谷胱甘肽S-转移酶的诱导作用。给予苯巴比妥后,S-芳基和S-芳烷基酶的比活性增加了60-80%,而S-环氧化物和S-烷基的活性增加了30-40%。在追踪诱导顺序时,发现前两种活性在观察到后两种活性增加之前达到峰值活性。3-甲基胆蒽和3,4-苯并芘均显示可诱导这四种酶活性,尽管没有观察到苯巴比妥所引起的成对活性之间的差异。药物诱导后,Vmax增加时Km没有变化,磺溴酞钠抑制的Ki也没有变化。在所研究的三种活性中,雌性大鼠的酶比活性显著较低,但S-烷基转移酶活性没有差异。然而,雄性和雌性大鼠对苯巴比妥反应时酶活性的比例增加是相同的。这些研究证明了一组胞质药物代谢酶的药物诱导作用以及这些活性中的性别差异。

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