Nakano E, Rabello-Gay M N, Pereira C A
Laboratório de Biologia Celular, Instituto Butantan, São Paulo, Brazil.
Teratog Carcinog Mutagen. 1996;16(1):37-48. doi: 10.1002/(SICI)1520-6866(1996)16:1<37::AID-TCM5>3.0.CO;2-H.
The genotoxic potential of the pyrethroid flumethrin was evaluated by using the combined protocol of metaphase analysis and micronucleus test in vivo in mouse bone marrow. The dermal route was tested in a single treatment and the intraperitoneal (i.p.) route in a single and a multiple treatment. Flumethrin showed a cytotoxic effect on both myelopoiesis and erythropoiesis, as evidenced by a reduction in the mitotic index and in polychromatic erythrocyte values. An increase in the frequency of gaps after the dermal exposure and of breaks only at the highest dose tested in the i.p. treatment indicates a weak clastogenic potential of the compound. A significant increase in the frequency of micronucleated polychromatic erythrocytes was observed after single and multiple i.p. treatments. In the latter, the induction of micronuclei was highly significant but not accompanied by an increase in breaks. This may indicate that the clastogenic effect might not account by itself for the induction of micronuclei, which could also have arisen from an aneugenic potential of flumethrin.
通过在小鼠骨髓中进行体内中期分析和微核试验的联合方案,评估了拟除虫菊酯氟氯氰菊酯的遗传毒性潜力。经皮途径采用单次处理进行测试,腹腔注射(i.p.)途径采用单次和多次处理进行测试。氟氯氰菊酯对骨髓生成和红细胞生成均显示出细胞毒性作用,有丝分裂指数和多色红细胞值降低证明了这一点。经皮暴露后间隙频率增加,仅在腹腔注射处理的最高测试剂量下出现断裂,表明该化合物的致断裂潜力较弱。单次和多次腹腔注射处理后,观察到微核多色红细胞频率显著增加。在多次处理中,微核的诱导非常显著,但没有伴随断裂增加。这可能表明,致断裂效应本身可能无法解释微核的诱导,微核也可能源于氟氯氰菊酯的非整倍体潜力。