Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse Spleen

Abstract The endocrine disruptor bisphenol A (BPA) and the pharmaceutical 17α-ethinyl estradiol (EE) are synthetic chemicals with estrogen-like activities. Despite ubiquitous human exposure to BPA, and the wide-spread clinical use of EE as oral contraceptive adjuvant, the impact of these estrogenic...

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Main Authors: Robin B. Gear, Scott M. Belcher
Format: Article
Language:English
Published: Nature Publishing Group 2017-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-00961-8
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spelling doaj-3fa22a9efb97409fa22da9620e9c65b82020-12-08T02:46:44ZengNature Publishing GroupScientific Reports2045-23222017-04-017111210.1038/s41598-017-00961-8Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse SpleenRobin B. Gear0Scott M. Belcher1Department of Pharmacology and Cell Biophysics, University of Cincinnati College of MedicineDepartment of Pharmacology and Cell Biophysics, University of Cincinnati College of MedicineAbstract The endocrine disruptor bisphenol A (BPA) and the pharmaceutical 17α-ethinyl estradiol (EE) are synthetic chemicals with estrogen-like activities. Despite ubiquitous human exposure to BPA, and the wide-spread clinical use of EE as oral contraceptive adjuvant, the impact of these estrogenic endocrine disrupting chemicals (EDCs) on the immune system is unclear. Here we report results of in vivo dose response studies that analyzed the histology and microstructural changes in the spleen of adult male and female CD-1 mice exposed to 4 to 40,000 μg/kg/day BPA or 0.02 to 2 μg/kg/day EE from conception until 12–14 weeks of age. Results of that analysis indicate that both BPA and EE have dose- and sex-specific impacts on the cellular and microanatomical structures of the spleens that reveal minor alterations in immunomodulatory and hematopoietic functions. These findings support previous studies demonstrating the murine immune system as a sensitive target for estrogens, and that oral exposures to BPA and EE can have estrogen-like immunomodulatory affects in both sexes.https://doi.org/10.1038/s41598-017-00961-8
collection DOAJ
language English
format Article
sources DOAJ
author Robin B. Gear
Scott M. Belcher
spellingShingle Robin B. Gear
Scott M. Belcher
Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse Spleen
Scientific Reports
author_facet Robin B. Gear
Scott M. Belcher
author_sort Robin B. Gear
title Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse Spleen
title_short Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse Spleen
title_full Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse Spleen
title_fullStr Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse Spleen
title_full_unstemmed Impacts of Bisphenol A and Ethinyl Estradiol on Male and Female CD-1 Mouse Spleen
title_sort impacts of bisphenol a and ethinyl estradiol on male and female cd-1 mouse spleen
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-04-01
description Abstract The endocrine disruptor bisphenol A (BPA) and the pharmaceutical 17α-ethinyl estradiol (EE) are synthetic chemicals with estrogen-like activities. Despite ubiquitous human exposure to BPA, and the wide-spread clinical use of EE as oral contraceptive adjuvant, the impact of these estrogenic endocrine disrupting chemicals (EDCs) on the immune system is unclear. Here we report results of in vivo dose response studies that analyzed the histology and microstructural changes in the spleen of adult male and female CD-1 mice exposed to 4 to 40,000 μg/kg/day BPA or 0.02 to 2 μg/kg/day EE from conception until 12–14 weeks of age. Results of that analysis indicate that both BPA and EE have dose- and sex-specific impacts on the cellular and microanatomical structures of the spleens that reveal minor alterations in immunomodulatory and hematopoietic functions. These findings support previous studies demonstrating the murine immune system as a sensitive target for estrogens, and that oral exposures to BPA and EE can have estrogen-like immunomodulatory affects in both sexes.
url https://doi.org/10.1038/s41598-017-00961-8
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