Dean R G, Bynum G, Jacobson-Kram D, Hadley E
Mutat Res. 1983 Nov;111(3):419-27. doi: 10.1016/0027-5107(83)90037-4.
Activation of polycyclic aromatic hydrocarbons (PAHs) was examined in the Reuber H4-II-E established cell line without the use of exogenous enzyme preparations. Metabolism of PAHs to genotoxic products was determined by the induction of sister-chromatid exchanges (SCEs). The induction of SCEs followed a dose-response pattern with plateaus at high doses of PAH. The effects of metabolic enzyme inducers (3-methylcholanthrene, phenobarbital, Aroclor 1254) and the epoxide hydrase inhibitor 1,1,1-trichloropropylene oxide were assessed as changes in SCE induction and enhanced production of water-soluble metabolites. Results indicate that Reuber H4-II-E cells can be employed in the testing of carcinogens activated by the P1-450 monooxygenase system and would be a useful in vitro system for the study of mechanisms of metabolic induction and their effect on genetic toxicity.
在不使用外源性酶制剂的情况下,对鲁伯H4-II-E建立的细胞系中多环芳烃(PAHs)的活化进行了研究。通过姐妹染色单体交换(SCEs)的诱导来确定PAHs向遗传毒性产物的代谢。SCEs的诱导呈现剂量反应模式,在高剂量PAH时出现平台期。评估了代谢酶诱导剂(3-甲基胆蒽、苯巴比妥、多氯联苯混合物Aroclor 1254)和环氧化物水解酶抑制剂1,1,1-三氯环氧丙烷对SCE诱导变化和水溶性代谢物产量增加的影响。结果表明,鲁伯H4-II-E细胞可用于测试由P1-450单加氧酶系统活化的致癌物,并且将是研究代谢诱导机制及其对遗传毒性影响的有用体外系统。