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Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats
Bisphenol A (BPA) is widely used in manufacturing industries. It is commonly detected in the environment and was reported to exert oestrogenic effects which may be harmful to the reproductive system. The present study was carried out to observe the effects of oral administration of BPA on the develo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Leibniz Research Centre for Working Environment and Human Factors
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464354/ https://www.ncbi.nlm.nih.gov/pubmed/26417249 |
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author | Gurmeet, KSS Rosnah, I Normadiah, MK Das, Srijit Mustafa, AM |
author_facet | Gurmeet, KSS Rosnah, I Normadiah, MK Das, Srijit Mustafa, AM |
author_sort | Gurmeet, KSS |
collection | PubMed |
description | Bisphenol A (BPA) is widely used in manufacturing industries. It is commonly detected in the environment and was reported to exert oestrogenic effects which may be harmful to the reproductive system. The present study was carried out to observe the effects of oral administration of BPA on the development of the reproductive organs and plasma sex hormone levels in prepubertal male Sprague-Dawley (SD) rats. Prepubertal male SD rats (n=8 in each group) were administered BPA in the doses of 1, 5, 10 and 100 mg/kg BW (body weight) via oral gavage for a period of 6 weeks. The control animals received the vehicle for BPA (Tween 80 in distilled water). Following 6 weeks of BPA exposure, the rats exhibited less evidence of spermatogenesis. There was seminiferous epithelial damage which included disruption of intercellular junctions and sloughing of germ cells into the seminiferous tubular lumen. Furthermore, the lumina of the seminiferous tubules and the epididymis of these animals were filled with immature germ cells and cellular debris. This damage may lead to the significant reduction in the seminiferous tubular diameter in BPA-treated animals. These findings were associated with the significant lower plasma testosterone and 17β-oestradiol levels. There was no significant difference between the body weight gain, the absolute as well as relative testis weight or epididymal weight of BPA-treated animals when compared to the control animals. The findings provided further evidence of the detrimental effects of BPA on the male reproductive system. |
format | Online Article Text |
id | pubmed-4464354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
spelling | pubmed-44643542015-09-28 Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats Gurmeet, KSS Rosnah, I Normadiah, MK Das, Srijit Mustafa, AM EXCLI J Original Article Bisphenol A (BPA) is widely used in manufacturing industries. It is commonly detected in the environment and was reported to exert oestrogenic effects which may be harmful to the reproductive system. The present study was carried out to observe the effects of oral administration of BPA on the development of the reproductive organs and plasma sex hormone levels in prepubertal male Sprague-Dawley (SD) rats. Prepubertal male SD rats (n=8 in each group) were administered BPA in the doses of 1, 5, 10 and 100 mg/kg BW (body weight) via oral gavage for a period of 6 weeks. The control animals received the vehicle for BPA (Tween 80 in distilled water). Following 6 weeks of BPA exposure, the rats exhibited less evidence of spermatogenesis. There was seminiferous epithelial damage which included disruption of intercellular junctions and sloughing of germ cells into the seminiferous tubular lumen. Furthermore, the lumina of the seminiferous tubules and the epididymis of these animals were filled with immature germ cells and cellular debris. This damage may lead to the significant reduction in the seminiferous tubular diameter in BPA-treated animals. These findings were associated with the significant lower plasma testosterone and 17β-oestradiol levels. There was no significant difference between the body weight gain, the absolute as well as relative testis weight or epididymal weight of BPA-treated animals when compared to the control animals. The findings provided further evidence of the detrimental effects of BPA on the male reproductive system. Leibniz Research Centre for Working Environment and Human Factors 2014-02-18 /pmc/articles/PMC4464354/ /pubmed/26417249 Text en Copyright © 2014 Gurmeet et al. http://www.excli.de/documents/assignment_of_rights.pdf This is an Open Access article distributed under the following Assignment of Rights http://www.excli.de/documents/assignment_of_rights.pdf. You are free to copy, distribute and transmit the work, provided the original author and source are credited. |
spellingShingle | Original Article Gurmeet, KSS Rosnah, I Normadiah, MK Das, Srijit Mustafa, AM Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats |
title | Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats |
title_full | Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats |
title_fullStr | Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats |
title_full_unstemmed | Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats |
title_short | Detrimental effects of bisphenol A on development and functions of the male reproductive system in experimental rats |
title_sort | detrimental effects of bisphenol a on development and functions of the male reproductive system in experimental rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464354/ https://www.ncbi.nlm.nih.gov/pubmed/26417249 |
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