Mühlenfeld K, Langner A
Institute of Pharmacy, Humboldt University, Berlin, Germany.
Pharmazie. 2001 Apr;56(4):329-31.
In this study the activity of Cytochrome P 450 (CYP) enzymes in isolated spleen lymphocytes of Wistar rats was estimated. 7-Ethoxyresorufin-O-deethylase was analysed to determine the activity of CYP 1A1/2. The activity was increased 2.2-fold by pretreating the animals with 3-methylcholanthrene, and 1.3-fold after the addition of the mitogen concanavalin A to the lymphocyte culture. Pretreatment of the rats with phenobarbitone did not enhance the basal enzyme activity. To estimate reductive activities the azoreduction of 4-(N,N-dimethyl-amino)azobenzene was analysed. Again detectable turnovers were found which could be increased 4-fold after the addition of concanavalin A. Azo-reductase activity could also be increased 2-fold after clofibrate was added to the lymphocyte cultures, and was decreased by adding metyrapone so that it was concluded that azoreduction may be partly due to the CYP 4A-family.
在本研究中,对Wistar大鼠分离的脾淋巴细胞中细胞色素P 450(CYP)酶的活性进行了评估。分析了7-乙氧基试卤灵-O-脱乙基酶以确定CYP 1A1/2的活性。用3-甲基胆蒽预处理动物后,该活性增加了2.2倍,在淋巴细胞培养物中加入促有丝分裂剂刀豆球蛋白A后,活性增加了1.3倍。用苯巴比妥预处理大鼠并未增强基础酶活性。为了评估还原活性,分析了4-(N,N-二甲基氨基)偶氮苯的偶氮还原。再次发现了可检测到的周转率,在加入刀豆球蛋白A后可增加4倍。在淋巴细胞培养物中加入氯贝丁酯后,偶氮还原酶活性也可增加2倍,而加入甲吡酮后则降低,因此得出结论,偶氮还原可能部分归因于CYP 4A家族。