Differential effects of bisphenol A and estradiol on rat spermatogenesis' establishment

被引:32
作者
Brouard, Vanessa [1 ,2 ,3 ]
Guenona, Isabelle [1 ,2 ,3 ]
Bouraima-Lelong, Helene [1 ,2 ,3 ]
Delalande, Christelle [1 ,2 ,3 ]
机构
[1] Normandie Univ, Caen, France
[2] UNICAEN, EA2608, Esplanade Paix,CS 14032, F-14032 Caen 5, France
[3] INRA, USC 1377, F-14032 Caen, France
关键词
Bisphenol A (BPA); Estradiol (E2); Spermatogenesis; Blood testis barrier (BTB); BLOOD-TESTIS BARRIER; SPERMATOGONIAL CELL-PROLIFERATION; COUPLED RECEPTOR 30; ESTROGEN-RECEPTOR; ER-BETA; EXPRESSION; EXPOSURE; MOUSE; APOPTOSIS; GAMMA;
D O I
10.1016/j.reprotox.2016.05.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several studies have highlighted the negative effects of bisphenol A (BPA), a chemical compound with estrogenic activity, on reproductive health. To elucidate the impact of BPA on spermatogenesis' establishment and mechanisms of action of BPA and 17 beta-estradiol (E2), as both can be found in the environment, we exposed rats to BPA (50 mu g/kg bw/day of BPA), E2 (20 mu g/kg bw/day of E2) and BPA+E2 from 15 to 30 days post-partum. Histological and gene expression studies revealed that BPA and BPA+E2 exposures promoted spermatogenesis establishment whereas E2 alone delayed it. Then, a decrease in gene expression of blood-testis-barrier (BTB) proteins was observed in all treated groups. Therefore, our study has demonstrated a differential effect of BPA and E2 exposures on spermatogenesis establishment in prepubertal rats and a deleterious effect of these chemicals on BTB establishment. Thus, the effects of BPA seem to be mediated by receptors other than estrogen receptors. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:49 / 61
页数:13
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