Lack of effects for dietary exposure of bisphenol A during in utero and lactational periods on reproductive development in rat offspring

The potential for health effects on humans with exposure to bisphenol A (BPA) has raised concerns, and the adverse effects of low-dose exposure to BPA on reproduction have been controversial. The purpose of the present study was to investigate the effects of low-dose exposure to BPA on reproductive...

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Veröffentlicht in:Journal of toxicological sciences 2012/06/01, Vol.37(3), pp.565-573
Hauptverfasser: Kobayashi, Kenichi, Kubota, Hisayo, Ohtani, Katsumi, Hojo, Rieko, Miyagawa, Muneyuki
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Sprache:eng
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Zusammenfassung:The potential for health effects on humans with exposure to bisphenol A (BPA) has raised concerns, and the adverse effects of low-dose exposure to BPA on reproduction have been controversial. The purpose of the present study was to investigate the effects of low-dose exposure to BPA on reproductive development in F1 rat offspring. Pregnant female Sprague-Dawley rats (F0) were fed a diet containing low doses of BPA (0, 0.33, 3.3, or 33 ppm) from gestational day (GD) 6 through postnatal day (PND) 21. The weanlings (F1) from all dose groups were fed a normal diet ad libitum after weaning and then were subjected to necropsy at 5 weeks or 3 months of age. No BPA-related changes were observed in body weight or weight of any of the major reproductive organs in F1 males and females. Epididymis weight was significantly lower only in 3-month-old F1 males exposed to 33 ppm BPA. Anogenital distance (AGD), the ratio of AGD to the cube root of body weight, and relative ovary weight were significantly lower in 5-week-old F1 females exposed to 3.3 and 33 ppm BPA, but significant differences were not observed in 3-month-old females. There were no BPA-related effects on cauda epididymal sperm motility in 3-month-old F1 males. Plasma reproductive steroid hormone concentrations were not altered among groups in either sex. These outcomes indicate that low-dose exposure to BPA in the diet does not adversely affect reproductive development in F1 rat offspring.
ISSN:0388-1350
1880-3989
DOI:10.2131/jts.37.565