| Literature DB >> 23548413 |
Dong Xia1, Nahid Parvizi, Yuchuan Zhou, Kesi Xu, Hui Jiang, Rongjie Li, Yiqiong Hang, Yang Lu.
Abstract
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.Entities:
Keywords: fenvalerate; intergenerational action; methylation; mice; reproductive function
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Year: 2013 PMID: 23548413 PMCID: PMC3795420 DOI: 10.1177/1933719113483015
Source DB: PubMed Journal: Reprod Sci ISSN: 1933-7191 Impact factor: 3.060