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应用遗传毒理短期测试研究氰戊菊酯致突变性
引用本文:周志俊 邵玉芬. 应用遗传毒理短期测试研究氰戊菊酯致突变性[J]. 毒理学杂志, 1993, 7(3): 141-143
作者姓名:周志俊 邵玉芬
作者单位:上海医科大学公共卫生学院 200032(周志俊,邵玉芬,汪敏,程蓓,黄雷鸣,屈家瑛),上海医科大学公共卫生学院 200032(薛寿征)
摘    要:报道的氰戊菊酯致突变性结果不一,为此用多种方法研究了氰戊菊酯标准品和工业品的致突变性。结果发现:小鼠骨髓多染红细胞微核试验阴性,但见雄性较大剂量时有随剂量增高趋势。小鼠睾丸初级精母细胞染色体数目畸变阴性,染色体结构畸变阳性。人体外周血淋巴细胞SCE频率虽与阴性对照比差别有显著意义,但无剂量反应关系,为阴性。人体外周血淋巴细胞UDS 试验,氰戊菊酯工业品油剂及日产粉剂呈较强阳性;标准品阳性较弱。综合上述材料,认为氰戊菊酯标准品是一弱阳性致突变剂,其工业品致突变性增强,可见杂质起了重要作用。因此,减少我国工业品中之杂质、提高纯度,可望降低其致突变性能。

关 键 词:氰戊菊酯 卫生毒理 致突变性 遗传毒理试验

Study on the mutagenicity of fenvalerate with short-term tests
Zhou Zhijun,Shao Yufen,Wang Min,Cheng Pei,Huang Leiming,Qu Jiaying,Xue Shouzheng School of Public Health,Shanghai Medical University Shanghai. Study on the mutagenicity of fenvalerate with short-term tests[J]. Journal of Toxicology, 1993, 7(3): 141-143
Authors:Zhou Zhijun  Shao Yufen  Wang Min  Cheng Pei  Huang Leiming  Qu Jiaying  Xue Shouzheng School of Public Health  Shanghai Medical University Shanghai
Affiliation:Zhou Zhijun,Shao Yufen,Wang Min,Cheng Pei,Huang Leiming,Qu Jiaying,Xue Shouzheng School of Public Health,Shanghai Medical University Shanghai 200032
Abstract:The mutagenicity of fenvalerate was studied with four short-term genotoxic tests. The res-ults showed that (1) fenvalerate did not induce micronulei in polychromatic erythrocytes ofmouse bone marrow; (2) fenvalerate could induce the structure aberrations, but not the num-erical aberrations in primary spermatogenic cells of mice; (3) sister chromatid exchangefrequencies were slightly but significantly increased in cultured human peripheral blood lymp-ocytes in vitro; and (4) fenvalerate enhanced the unscheduled DNA synthesis of human pe-ripheral blood lymphocytes iu vitro. These results indicated that fenvalerate is a weak muta-en and this effect was more prominant by technical product which could contain unkown mu-tagenic impurities. Therefore, the purity of the product of fenvalerate should be improved toeliminate the mutagenic potential.
Keywords:Micronucleus assay  SCE assay  UDS assay  Chromosomal aberrations in pr primary spermatogenic cells
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