Taylor G, Houston J B, Elcombe C R
Xenobiotica. 1985 Mar;15(3):243-9. doi: 10.3109/00498258509045355.
The characteristics of induction of rat-hepatic microsomal mono-oxygenase activity by promethazine and isosafrole have been investigated and compared with the classic inducers phenobarbitone and beta-naphthoflavone. Both promethazine and isosafrole pretreatments result in increased cytochromes P-450, and enhanced NADPH-cytochrome c reductase, aminopyrine N-demethylase, dichloronitroanisole O-demethylase, ethoxycoumarin O-deethylase and ethoxyresorufin O-deethylase activity. Isosafrole but not promethazine increased the liver to body weight ratio. It is concluded that promethazine and isosafrole pretreatment produces an induction of the rat-hepatic microsomal mono-oxygenase system which shows both phenobarbitone- and polycyclic aromatic hydrocarbon-type characteristics.
已对异丙嗪和异黄樟素诱导大鼠肝微粒体单加氧酶活性的特性进行了研究,并与经典诱导剂苯巴比妥和β-萘黄酮进行了比较。异丙嗪和异黄樟素预处理均导致细胞色素P-450增加,以及NADPH-细胞色素c还原酶、氨基比林N-脱甲基酶、二氯硝基苯甲醚O-脱甲基酶、乙氧香豆素O-脱乙基酶和乙氧试卤灵O-脱乙基酶活性增强。异黄樟素而不是异丙嗪增加了肝体比。结论是,异丙嗪和异黄樟素预处理可诱导大鼠肝微粒体单加氧酶系统,该系统表现出苯巴比妥型和多环芳烃型特征。