Impact of perinatal bisphenol A and 17β estradiol exposure: Comparing hormone receptor response

• Autor(a) principal: Leonel, Ellen Cristina Rivas [UNESP]
• Data de Publicação: 2020
• Outros Autores: Campos, Silvana Gisele Pegorin, Guerra, Luiz Henrique Alves [UNESP], Bedolo, Carolina Marques [UNESP], Vilamaior, Patrícia Simone Leite [UNESP], Calmon, Marilia Freitas [UNESP], Rahal, Paula [UNESP], Amorim, Christiani Andrade, Taboga, Sebastião Roberto [UNESP]
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNESP
• Texto Completo: http://dx.doi.org/10.1016/j.ecoenv.2019.109918; http://hdl.handle.net/11449/201374
• topic: Estrogen; Estrogen receptor; Mammary gland; Mongolian gerbil; Progesterone receptor; Xenoestrogen

Hormonal regulation controls mammary gland (MG) development. Therefore some hormone-related factors can disrupt the early phases of MGs development, making the gland more susceptible to long term modifications in its response to circulating hormones. Endocrine disruptors, such as bisphenol A (BPA), are able to cause alterations in hormone receptor expression, leading to changes in the cell proliferation index, which may expose the tissue to neoplastic alterations. Thus, we evaluated the variations in hormone receptor expression in the MG of 6-month old Mongolian gerbils exposed to BPA and 17β estradiol during the perinatal period. Receptors for estrogen alpha (ERα), beta (ERβ), progesterone (PGR), prolactin (PRL-R), and co-localization of connexin 43 (Cx43) and ERα in gerbils were analyzed, and serum concentrations of estradiol and progesterone were assessed. No alterations in body, liver, and ovary-uterus complex weights were observed. However, there was an increase in epithelial ERα expression in the 17β estradiol (E2) group and in PGR in the BPA group. Although immunohistochemistry did not show alterations in ERβ expression, western blotting revealed a decrease in this protein in the BPA group. PRL-R was more present in epithelial cells in the vehicle control (VC), E2, and BPA groups in comparison to the intact control group. Cx43 was more frequent in E2 and BPA groups, suggesting a protective response from the gland against possible malignancy. Serum concentration of estradiol reduced in VC, E2, and BPA groups, confirming that alterations also impacts steroid levels. Consequently, perinatal exposure to BPA and the reference endogenous estrogen, 17β estradiol, are able to increase the tendency of endocrine disruption in MG in a long term manner, since repercussions are observed even 6 months after exposure.