Journal
BIOLOGY OF REPRODUCTION
Volume 94, Issue 1, Pages -Publisher
OXFORD UNIV PRESS INC
DOI: 10.1095/biolreprod.115.134452
Keywords
androgens; brominated flame retardants; catalase; endocrine disrupters; folliculogenesis; HBCDD; insulin-like factor 3; ovary; oxidative stress; PBDE; steroidogenesis; toxicology
Categories
Funding
- Canadian Institutes of Health Research (CIHR) Institute for Human Development, Child, and Youth Health [RHF100625]
- NSERC Create award from Reseau Quebecois en Reproduction
- PLCL of a Fonds de recherche du Quebec-Sante fellowship
- Eunice Kennedy Shriver NICHD/NIH (SCCPIR) grant [U54-HD28934]
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Brominated flame retardants (BFRs) are incorporated into various consumer products to prevent flame propagation. These compounds leach into the domestic environment, resulting in chronic exposure and contamination. Pregnancy failure is associated with high levels of BFRs in human follicular fluid, raising serious questions regarding their impact on female reproductive health. The goal of this study is to elucidate the effects of an environmentally relevant BFR mixture on female rat ovarian functions (i.e., folliculogenesis and steroidogenesis). A BFR dietary mixture formulated to mimic the relative BFR congener levels in North American house dust was administered to adult female Sprague-Dawley rats from 2 to 3 wk before mating until Gestational Day 20; these diets were designed to deliver nominal doses of 0, 0.06, 20, or 60 mg/kg/day of the BFR mixture. Exposure to BFRs triggered an approximately 50% increase in the numbers of preantral and antral follicles and an enlargement of the antral follicles in the ovaries of the dams. A significant reduction in the expression of catalase, an antioxidant enzyme, and downregulation of the expression of insulin-like factor 3 (Insl3) and 17alpha-hydroxylase (Cyp17a1) were observed in the ovary. In addition, BFR exposure affected steroidogenesis; we observed a significant decrease in circulating 17-hydroxypregnenolone and an increase in testosterone concentrations in BFR-exposed dams. Thus, BFRs target ovarian function in the rat, adversely affecting both folliculogenesis and steroidogenesis.
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