Cytotoxicity and DNA damage of five organophosphorus pesticides mediated by oxidative stress in PC12 cells and protection by vitamin E

被引:45
作者
Lu, Xian T. [3 ,4 ]
Ma, Yun [2 ]
Wang, Cui [2 ]
Zhang, Xiao F. [2 ]
Jin, Da Q. [1 ]
Huang, Chang J. [1 ]
机构
[1] Wenzhou Med Coll, Inst Watershed Sci & Environm Ecol, Wenzhou 325035, Peoples R China
[2] Zhejiang Univ Technol, Res Ctr Environm Sci, Coll Biol & Environm Engn, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, MOE Key Lab Environm Remediat & Ecosyst Hlth, Coll Environm & Resource Sci, Hangzhou 310003, Zhejiang, Peoples R China
[4] Hangzhou Dianzi Univ, Inst Environm Sci & Engn, Mat & Environm Engn Sch, Hangzhou, Zhejiang, Peoples R China
关键词
Organophosphorous insecticides; oxidative stress; cytotoxicity; genotoxicity; IN-VITRO; COMET ASSAY; INSECTICIDE; MALATHION; APOPTOSIS; GENOTOXICITY; BIFENTHRIN; TOXICITY; ENANTIOSELECTIVITY; INDUCTION;
D O I
10.1080/03601234.2012.663312
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Previous studies have demonstrated that pesticides could induce cytotoxicity and genotoxicity in vivo and in vitro, and that oxidative stress may be an important factor involved. However, investigations comparing the capability of different organophosphorous (OP) compounds to induce cytotoxicity, genotoxicity and oxidative stress are limited. Hence, the aim of this paper was to access the cytotoxic and genotoxic effects of five OPs or metabolites, Acephate (ACE), Methamidophos (MET), Chloramidophos (CHL), Malathion (MAT) and Malaoxon (MAO), and to clarify the role of oxidative stress, using PC12 cells. The results demonstrated that MET, MAT and MAO caused significant inhibition of cell viability and increased DNA damage in PC12 cells at 40 mg L-1. MAO was more toxic than the other OPs. ACE, MET, MAT and MAO increased the levels of intracellular reactive oxygen species (ROS) and malondialdehyde (MDA), and decreased the activity of superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH) at 20 mg L-1 and 40 mg L-1 to different degrees. Pre-treatment with vitamin E(600 mu M) caused a significant attenuation in the cytotoxic and genotoxic effect; pre-treatment reversed subsequent OP-induced elevation of peroxidation products and the decline of anti-oxidant enzyme activities. These results indicate that oxidative damage is likely to be an initiating event that contributes to the OP-induced cytotoxicity.
引用
收藏
页码:445 / 454
页数:10
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