Sperm chromatin alteration and DNA damage by methyl-parathion, chlorpyrifos and diazinon and their oxon metabolites in human spermatozoa

被引:78
作者
Salazar-Arredondo, Elsa [1 ,2 ]
Solis-Heredia, Maria de Jesus [1 ]
Rojas-Garcia, Elizabeth [1 ,3 ]
Hernandez-Ochoa, Isabel [1 ]
Quintanilla-Vega, Betzabet [1 ]
机构
[1] CINVESTAV, Secc Externa Toxicol, IPN, Mexico City 07360, DF, Mexico
[2] Univ Nacl Autonoma Mexico, FES Iztacala, Mexico City 97150, DF, Mexico
[3] Univ Autonoma Nayarit, Direcc Fortalecimiento Invest, Tepic 63190, Nayarit, Mexico
关键词
oxons toxicity; methyl-parathion; chlorpyrifos; diazinon; sperm chromatin; sperm DNA;
D O I
10.1016/j.reprotox.2008.05.055
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extensive use of organophosphorous pesticides (OP) by young men represents a public health problem. Toxicity of OP mainly results in neurotoxicity due to their oxygen analogues (oxons), formed during the OP oxidative activation. OP alter semen quality and sperm chromatin and DNA at different stages of spermatogenesis. Oxons are more toxic than the parent compounds; however, their toxicity to spermatogenic cells has not been reported. We evaluated sperm DNA damage by several OP compounds and their oxons in human spermatozoa from healthy volunteers incubated with 50-750 mu M of methyl-parathion (MePA), methyl-paraoxon (MePO), chlorpyrifos (CPF), chlorpyrifos-oxon (CPO), diazinon (DZN) or diazoxon (DZO). All concentrations were not cytotoxic (evaluated by eosin-Y exclusion), except 750 p,]VI MePO. Oxons were 15% to 10 times more toxic to sperm DNA(evaluated by the SCSA parameter, %DFI) than their corresponding parent compounds, at the following order: MePO > CPO = MePA > CPF > DZO > DZN, suggesting that oxon metabolites participate in OP sperm genotoxicity. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:455 / 460
页数:6
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