Genotoxicity Evaluation of Dimethoate to Experimental Mice by Micronucleus, Chromosome Aberration Tests, and Comet Assay

被引:20
作者
Ayed-Boussema, Imen [1 ]
Rjiba, Karima [1 ]
Mnasri, Nourhene [1 ]
Moussa, Amal [1 ]
Bacha, Hassen [1 ]
机构
[1] Fac Dent, Lab Res Biologically Compatible Cpds, Monastir 5019, Tunisia
关键词
dimethoate; genotoxicity; micronucleus test; chromosome aberration test; comet assay; mouse bone marrow cells; subchronic exposition; SISTER-CHROMATID EXCHANGES; IN-VITRO; ANTIOXIDANT STATUS; PERIPHERAL LYMPHOCYTES; PESTICIDES; INDUCTION; LIVER; RATS; ORGANOPHOSPHORUS; TOXICITY;
D O I
10.1177/1091581811423981
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dimethoate (DM) is an organophosphate insecticide with numerous uses on field and agricultural crops and ornamentals. Data concerning DM-acute genotoxicity are controversial and knowledge on its delayed effect is limited. For this reason, we aimed to further explore DM genotoxicity resulting from subchronic intoxication of experimental mice. Thus, DM was administered to mice at doses ranging from 1 to 30 mg/kg body weight for a period of 30 consecutive days. There was a significant increase (P < .05) in the frequency of micronucleated bone marrow cells following DM administration. Furthermore, the chromosome aberration assay revealed a significant increase in the percentage of chromosome abnormalities in a dose-dependent manner. Dimethoate was also found to induce significant DNA damage in mouse bone marrow cells as assessed by the comet assay. Altogether, our results showed that, after a subchronic exposure, DM was a genotoxic compound in experimental mice.
引用
收藏
页码:78 / 85
页数:8
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