Bisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.

The high incidence of prostate cancer (PCa) and benign prostatic hypertrophy (BPH) in elderly men is a cause of increasing public health concern. In recent years, various environmental endocrine disruptors, such as bisphenol A (BPA), have been shown to disrupt sexual organs, including the prostate g...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Beatriz Castro, Pilar Sánchez, Jesús M Torres, Ovidiu Preda, Raimundo G del Moral, Esperanza Ortega
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/4afadf89e9074a72bb9e57c3662e9cc4
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:4afadf89e9074a72bb9e57c3662e9cc4
record_format dspace
spelling oai:doaj.org-article:4afadf89e9074a72bb9e57c3662e9cc42021-11-18T07:58:29ZBisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.1932-620310.1371/journal.pone.0055905https://doaj.org/article/4afadf89e9074a72bb9e57c3662e9cc42013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23405234/?tool=EBIhttps://doaj.org/toc/1932-6203The high incidence of prostate cancer (PCa) and benign prostatic hypertrophy (BPH) in elderly men is a cause of increasing public health concern. In recent years, various environmental endocrine disruptors, such as bisphenol A (BPA), have been shown to disrupt sexual organs, including the prostate gland. However, the mechanisms underlying these effects remain unclear. Because androgens and estrogens are important factors in prostate physiopathology, our objective was to examine in rat ventral prostate the effects of adult exposure to BPA on 5α-Reductase isozymes (5α-R types 1, 2, and 3) and aromatase, key enzymes in the biosynthesis of dihydrotestosterone and estradiol, respectively. Adult rats were subcutaneously injected for four days with BPA (25, 50, 300, or 600 µg/Kg/d) dissolved in vehicle. Quantitative RT-PCR, western blot and immunohistochemical analyses showed lower mRNA and protein levels of 5α-R1 and 5α-R2 in BPA-treated groups versus controls but higher mRNA levels of 5α-R3, recently proposed as a biomarker of malignancy. However, BPA treatment augmented mRNA and protein levels of aromatase, whose increase has been described in prostate diseases. BPA-treated rats also evidenced a higher plasma estradiol/testosterone ratio, which is associated with prostate disease. Our results may offer new insights into the role of BPA in the development of prostate disease and may be of great value for studying the prostate disease risk associated with exposure to BPA in adulthood.Beatriz CastroPilar SánchezJesús M TorresOvidiu PredaRaimundo G del MoralEsperanza OrtegaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 2, p e55905 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Beatriz Castro
Pilar Sánchez
Jesús M Torres
Ovidiu Preda
Raimundo G del Moral
Esperanza Ortega
Bisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.
description The high incidence of prostate cancer (PCa) and benign prostatic hypertrophy (BPH) in elderly men is a cause of increasing public health concern. In recent years, various environmental endocrine disruptors, such as bisphenol A (BPA), have been shown to disrupt sexual organs, including the prostate gland. However, the mechanisms underlying these effects remain unclear. Because androgens and estrogens are important factors in prostate physiopathology, our objective was to examine in rat ventral prostate the effects of adult exposure to BPA on 5α-Reductase isozymes (5α-R types 1, 2, and 3) and aromatase, key enzymes in the biosynthesis of dihydrotestosterone and estradiol, respectively. Adult rats were subcutaneously injected for four days with BPA (25, 50, 300, or 600 µg/Kg/d) dissolved in vehicle. Quantitative RT-PCR, western blot and immunohistochemical analyses showed lower mRNA and protein levels of 5α-R1 and 5α-R2 in BPA-treated groups versus controls but higher mRNA levels of 5α-R3, recently proposed as a biomarker of malignancy. However, BPA treatment augmented mRNA and protein levels of aromatase, whose increase has been described in prostate diseases. BPA-treated rats also evidenced a higher plasma estradiol/testosterone ratio, which is associated with prostate disease. Our results may offer new insights into the role of BPA in the development of prostate disease and may be of great value for studying the prostate disease risk associated with exposure to BPA in adulthood.
format article
author Beatriz Castro
Pilar Sánchez
Jesús M Torres
Ovidiu Preda
Raimundo G del Moral
Esperanza Ortega
author_facet Beatriz Castro
Pilar Sánchez
Jesús M Torres
Ovidiu Preda
Raimundo G del Moral
Esperanza Ortega
author_sort Beatriz Castro
title Bisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.
title_short Bisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.
title_full Bisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.
title_fullStr Bisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.
title_full_unstemmed Bisphenol A exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.
title_sort bisphenol a exposure during adulthood alters expression of aromatase and 5α-reductase isozymes in rat prostate.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/4afadf89e9074a72bb9e57c3662e9cc4
work_keys_str_mv AT beatrizcastro bisphenolaexposureduringadulthoodaltersexpressionofaromataseand5areductaseisozymesinratprostate
AT pilarsanchez bisphenolaexposureduringadulthoodaltersexpressionofaromataseand5areductaseisozymesinratprostate
AT jesusmtorres bisphenolaexposureduringadulthoodaltersexpressionofaromataseand5areductaseisozymesinratprostate
AT ovidiupreda bisphenolaexposureduringadulthoodaltersexpressionofaromataseand5areductaseisozymesinratprostate
AT raimundogdelmoral bisphenolaexposureduringadulthoodaltersexpressionofaromataseand5areductaseisozymesinratprostate
AT esperanzaortega bisphenolaexposureduringadulthoodaltersexpressionofaromataseand5areductaseisozymesinratprostate
_version_ 1718422662059917312