Chłopkiewicz B, Gruber B
Drug Institute, Warsaw, Poland.
Acta Pol Pharm. 1997 Nov-Dec;54(6):437-41.
Genotoxic activity of adriamycin and bleomycin in embryo cells from mice differing in anti-oxidant enzymes activity was investigated. The catalase activity in cultured in vitro embryo cells of C3H mice was 2.3-fold and superoxide dismutase 2.5-fold higher than of C57BL/10 mice. For genotoxicity evaluation, the micronucleus test in vitro was used. The results obtained indicated that the frequency of micronucleated cells in untreated C3H cultures was higher than in C57BL/10 cell cultures. The increase in micronuclei formation after treatment with adriamycin and bleomycin was higher in C57BL/10 than in C3H cells as compared with micronuclei in untreated cultures. The higher frequency of micronucleated cells in treated versus untreated C57BL/10 than C3H cell cultures may be caused by lower activity of anti-oxidant enzymes in C57BL/10 cells. It may suggest that DNA damage caused by adriamycin and bleomycin resulted from action of active oxygen species.
研究了阿霉素和博来霉素对抗氧化酶活性不同的小鼠胚胎细胞的遗传毒性作用。C3H小鼠体外培养胚胎细胞中的过氧化氢酶活性比C57BL/10小鼠高2.3倍,超氧化物歧化酶活性高2.5倍。为评估遗传毒性,采用了体外微核试验。所得结果表明,未处理的C3H培养物中微核细胞的频率高于C57BL/10细胞培养物。与未处理培养物中的微核相比,阿霉素和博来霉素处理后,C57BL/10细胞中微核形成的增加高于C3H细胞。处理过的C57BL/10细胞培养物与未处理的相比,微核细胞频率高于C3H细胞培养物,这可能是由于C57BL/10细胞中抗氧化酶活性较低所致。这可能表明,阿霉素和博来霉素引起的DNA损伤是由活性氧的作用导致的。