Panneerselvam N, Sinha S, Shanmugam G
Cancer Biology Division, School of Biological Sciences, Madurai Kamaraj University, India.
Mutat Res. 1995 Aug;344(1-2):69-72. doi: 10.1016/0165-1218(95)90040-3.
Cultured human lymphocytes were exposed to three different concentrations (2.5, 5.0 and 10.0 micrograms/ml) of fluchloralin for 24 and 48 h to assess chromosomal aberrations. A significant dose-dependent increase of chromatid type aberration was observed in these cells. Multiple aberrations (MA) were scored at all concentrations after 48 h treatment. To support these results we did micronucleus (MN) test using cytochalasin B to block cytokinesis. At lower concentrations (2.5 to 10.0 micrograms/ml) the frequency of MN induction was not significantly different. Higher concentrations of fluchloralin (20, 40 and 50 micrograms/ml) resulted in a significant dose dependent increase in number of micronucleated cells. This is the first report on genotoxic effects of fluchloralin in human cells.
将培养的人淋巴细胞暴露于三种不同浓度(2.5、5.0和10.0微克/毫升)的氟乐灵中24小时和48小时,以评估染色体畸变情况。在这些细胞中观察到染色单体型畸变呈显著的剂量依赖性增加。在处理48小时后,对所有浓度的多重畸变(MA)进行了评分。为了支持这些结果,我们使用细胞松弛素B进行胞质分裂阻滞,进行了微核(MN)试验。在较低浓度(2.5至10.0微克/毫升)下,微核诱导频率没有显著差异。较高浓度的氟乐灵(20、40和50微克/毫升)导致微核化细胞数量显著的剂量依赖性增加。这是关于氟乐灵对人细胞遗传毒性作用的首次报告。