کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2591225 1131803 2012 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Low oral doses of bisphenol A increase volume of the sexually dimorphic nucleus of the preoptic area in male, but not female, rats at postnatal day 21
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
Low oral doses of bisphenol A increase volume of the sexually dimorphic nucleus of the preoptic area in male, but not female, rats at postnatal day 21
چکیده انگلیسی

Perinatal treatment with relatively high doses of bisphenol A (BPA) appears to have little effect on volume of the rodent sexually dimorphic nucleus of the preoptic area (SDN-POA). However, doses more relevant to human exposures have not been examined. Here, effects of pre- and post-natal treatment with low BPA doses on SDN-POA volume of postnatal day (PND) 21 Sprague–Dawley rats were evaluated. Pregnant rats were orally gavaged with vehicle, 2.5 or 25.0 μg/kg BPA, or 5.0 or 10.0 μg/kg ethinyl estradiol (EE2) on gestational days 6–21. Beginning on the day after birth, offspring were orally treated with the same dose their dam had received. On PND 21, offspring (n = 10–15/sex/group; 1/sex/litter) were perfused and volume evaluation was conducted blind to treatment. SDN-POA outline was delineated using calbindin D28K immunoreactivity. Pairwise comparisons of the significant treatment by sex interaction indicated that neither BPA dose affected female volume. However, females treated with 5.0 or 10.0 μg/kg EE2 exhibited volumes that were larger than same-sex controls, respectively (p < 0.001). Males treated with either BPA dose or 10.0 μg/kg/day EE2 had larger volumes than same-sex controls (p < 0.006). These data indicate that BPA can have sex-specific effects on SDN-POA volume and that these effects manifest as larger volumes in males. Sensitivity of the methodology as well as the treatment paradigm was confirmed by the expected EE2-induced increase in female volume. These treatment effects might lead to organizational changes within sexually dimorphic neuroendocrine pathways which, if persistent, could theoretically alter adult reproductive physiology and socio-sexual behavior in rats.


► Pregnant rats were treated orally with bisphenol A (BPA) or ethinyl estradiol (EE2).
► After birth, offspring directly treated orally until weaning at postnatal (PND) 21.
► Sexually dimorphic nucleus of the preoptic area (SDN-POA) volume measured at PND 21.
► Female SDN-POA volume was larger in both EE2 groups, but no difference in BPA groups.
► Male SDN-POA volume was larger in both BPA groups and in 10 μg/kg EE2 group.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neurotoxicology and Teratology - Volume 34, Issue 3, May–June 2012, Pages 331–337
نویسندگان
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