1Institute of Animal Husbandry & Veterinary Sciences, Shanghai Academy of Agricultural Sciences, Shanghai, China.
Reprod Sci. 2013 Nov;20(11):1308-15. doi: 10.1177/1933719113483015. Epub 2013 Apr 2.
Fenvalerate (Fen), a synthetic pyrethroid insecticide, has been shown to have adverse effects on male reproductive system. Thus, the aim of the present study was to elucidate whether these adverse effects are passed from exposed male mice to their offspring. Adult male mice received Fen (10 mg/kg) daily for 30 days and mated with untreated females to produce offspring. Fenvalerate significantly changed the methylation status of angiotensin I-converting enzyme (Ace), forkhead box O3 (Foxo3a), huntingtin-associated protein 1 (Hap1), nuclear receptor subfamily 3 (Nr3c2), promyelocytic leukemia (Pml), and Prostaglandin F2 receptor negative regulator (Ptgfrn) genes in paternal mice sperm genomic DNA. Further, Fen significantly increased sperm abnormalities; serum testosterone and estradiol-17ß level in adult male (F0) and their male offspring (F1). Further, paternal Fen treatment significantly increased the length of estrous cycle, serum estradiol-17ß concentration in estrus, and progesterone levels in diestrus in female offspring (F1). These findings suggest that adverse effects of paternal Fen exposure on reproductive functions can be seen not only in treated males (F0) but also in their offsprings.
氰戊菊酯(Fen)是一种合成拟除虫菊酯杀虫剂,已被证明对雄性生殖系统有不良影响。因此,本研究旨在阐明这些不良影响是否会从暴露的雄性小鼠传递给它们的后代。成年雄性小鼠每天接受 Fen(10mg/kg)处理 30 天,并与未处理的雌性小鼠交配以产生后代。Fen 显著改变了雄性小鼠精子基因组 DNA 中血管紧张素 I 转化酶(Ace)、叉头框 O3(Foxo3a)、亨廷顿相关蛋白 1(Hap1)、核受体亚家族 3(Nr3c2)、早幼粒细胞白血病(Pml)和前列腺素 F2 受体负调节剂(Ptgfrn)基因的甲基化状态。此外,Fen 还显著增加了成年雄性(F0)及其雄性后代(F1)的精子畸形率和血清睾酮和雌二醇-17β水平。此外,父代 Fen 处理还显著增加了雌性后代(F1)的动情周期长度、动情期血清雌二醇-17β浓度和动情后期孕激素水平。这些发现表明,父代 Fen 暴露对生殖功能的不良影响不仅可以在处理过的雄性(F0)中看到,也可以在它们的后代中看到。