Hepatotoxicity and nephrotoxicity induced by the chlorpyrifos and chlorpyrifos-methyl metabolite, 3,5,6-trichloro-2-pyridinol, in orally exposed mice

被引:46
作者
Deng, Yongfeng [1 ]
Zhang, Yan [1 ]
Lu, Yifeng [1 ]
Zhao, Yanping [2 ]
Ren, Hongqiang [1 ]
机构
[1] Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Normal Univ, Sch Geog Sci, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
3,5,6-Trichloro-2-pyridinol; Organophosphorus insecticides; Subchronic effects; Metabolomics; Mice; WASTE-WATER; ORGANOPHOSPHATE PESTICIDE; DEVELOPMENTAL TOXICITY; OXIDATIVE STRESS; RATS; BRAIN; LIVER; IDENTIFICATION; DYSREGULATION; NEUROTOXICITY;
D O I
10.1016/j.scitotenv.2015.11.162
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
3,5,6-Trichloro-2-pyridinol (TCP) is a primary degradation product of chlorpyrifos and chlorpyrifos-methyl. TCP has longer half-life in soil and greater solubility in water than its parent compound, and cause wide contamination in environments. However, studies about the toxic effects of TCP are limited and outdate. In this study, 5 mg/kg/day, 50 mg/kg/day, and 150 mg/kg/day TCP were given to male mice through gavage for four weeks. As a result, the final body weights of TCP treated groups were significantly lower than control, and the relative organ weights of the liver and kidney were significantly higher than that of control. In addition, NMR-based metabolomics was used to investigate the toxic effects of TCP. It was found that a total of 39 serum metabolites were significantly changed in the TCP-treated groups, and these metabolites are related to hepatotoxicity and nephrotoxicity. These results were also confirmed by histopathology, serum biochemical, and oxidative stress analysis. In addition, metabolic disturbances due to TCP exposure were also observed based on altered metabolites. As far as we know, these results are the first to show the metabolomic toxicity of TCP, which warrants further research. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:507 / 514
页数:8
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