| Literature DB >> 26562050 |
Jiangfei Chen1, Yanyan Xiao1, Zengxin Gai1, Rong Li1, Zixu Zhu1, Chenglian Bai1, Robert L Tanguay2, Xiaojiang Xu3, Changjiang Huang4, Qiaoxiang Dong5.
Abstract
Bisphenol A (BPA), a high-volume chemical used to make polycarbonate plastic and epoxy resins, is a ubiquitous contaminant in environment and human body. To investigate the reproductive effects of long-term exposure to low concentrations of BPA, a two-generation study was conducted using the aquatic model species of zebrafish. Our findings revealed that exposure to 1nM (0.228μg/L) BPA for continuous two generations resulted in female-biased sex ratio in both F1 and F2 adult population, decreased sperm density, and decreased sperm quality as measured by motility, velocity, ATP content and lipid peroxidation in F1 and F2 males. Females were less sensitive to BPA exposures than males as no adverse effects were found in female gonads or gametes. Delayed hatching at 48hpf and increased malformation and mortality were found in the offspring from BPA exposed F2, but not F1 parents. Most importantly, the adverse effect on larval development and survival from BPA exposed F2 parents was paternal-specific, resulting mainly from BPA exposed males. Subsequent transcription analysis of F2 male gonads revealed dysregulated mitochondrial biogenesis and significant activation of non-canonical Wnt/planar cell polarity and Wnt/Calcium signaling pathways. Gene expression analysis of larvae from BPA exposed F2 parents showed significant reduced expression of DNA methyltransferases such as dnmt1, dnmt3, and dnmt5. In conclusion, low level BPA exposures for continuous two generations not only affects sex ratio and sperm quantity/quality in F1 and F2 adults, reproductive success in offspring from F2 parents, but also perturbs various molecular pathways potentially contributing to these BPA induced male-specific reproductive defects.Entities:
Keywords: BPA; Chronic exposure; Mitochondrial biogenesis; Sperm; Wnt signaling; Zebrafish
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Year: 2015 PMID: 26562050 PMCID: PMC6689195 DOI: 10.1016/j.aquatox.2015.10.020
Source DB: PubMed Journal: Aquat Toxicol ISSN: 0166-445X Impact factor: 4.964