Kliesch U, Adler I D
Institute of Mammalian Genetics, Society for Radiation and Environmental Research, Neuherberg, F.R.G.
Mutat Res. 1987 Nov;192(3):181-4. doi: 10.1016/0165-7992(87)90053-4.
Micronucleus tests were carried out in bone marrow of mice treated with 1-nitropropane, 2-nitropropane and cisplatin. For 1-nitropropane and 2-nitropropane the results were negative. With cisplatin a dose-dependent increase in the number of polychromatic erythrocytes with micronuclei was observed. The lowest positive dose was 0.1 mg/kg (P less than 0.001, Mann-Whitney-Wilcoxon test). The hepatocarcinogen 2-nitropropane showed clastogenic activity in human lymphocytes in vitro in the presence of S9 (Bauchinger et al., 1987). The negative results in bone marrow suggest that short-lived genotoxic metabolites may be formed in the liver but do not reach the bone marrow.
对用1-硝基丙烷、2-硝基丙烷和顺铂处理的小鼠骨髓进行了微核试验。对于1-硝基丙烷和2-硝基丙烷,结果为阴性。使用顺铂时,观察到含微核的多染性红细胞数量呈剂量依赖性增加。最低阳性剂量为0.1mg/kg(P<0.001,曼-惠特尼-威尔科克森检验)。肝癌致癌物2-硝基丙烷在S9存在的情况下,在体外人淋巴细胞中显示出致断裂活性(鲍辛格等人,1987年)。骨髓中的阴性结果表明,可能在肝脏中形成了短寿命的遗传毒性代谢物,但未到达骨髓。