Progesterone as a morphological regulatory factor of the male and female gerbil prostate

dc.contributor.authorFochi, Ricardo A.
dc.contributor.authorSantos, Fernanda C. A.
dc.contributor.authorGoes, Rejane M. [UNESP]
dc.contributor.authorTaboga, Sebastiao R. [UNESP]
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Federal de Goiás (UFG)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-12-03T13:11:06Z
dc.date.available2014-12-03T13:11:06Z
dc.date.issued2013-12-01
dc.description.abstractTestosterone (T) and oestrogen are the main active steroid hormones in the male and female reproductive system respectively. In female rodents progesterone (P4), together with testosterone and oestrogen, has an essential role in the regulation of the oestrous cycle, which influences the prostate physiology through their oscillations. In this work we investigated how the male and female prostate gland of Mongolian gerbils responds to surgical castration at the start of puberty and what are the effects of T, oestradiol (E2) and P4 replacement, using both quantitative and qualitative methods. We also examined the location of the main steroid receptors present in the prostate. In the castrated animals of both sexes an intense glandular regression, along with disorganization of the stromal compartment, and abundant hyperplasia was observed. The replacement of P4 secured a mild recovery of the glandular morphology, inducing the growth of secretory cells and restoring the androgen receptor (AR) cells. The administration of P4 and E2 eliminated epithelial hyperplasia and intensified gland hypertrophy, favouring the emergence of prostatic intraepithelial neoplasia (PIN). In animals treated with T and P4, even though there are some inflammatory foci and other lesions, the prostate gland revealed morphology closer to that of control animals. In summary, through the administration of P4, we could demonstrate that this hormone has anabolic characteristics, promoting hyperplasia and hypertrophy, mainly in the epithelial compartment. When combined with E2 and T, there is an accentuation of glandular hypertrophy that interrupts the development of hyperplasia and ensures the presence of a less dysplastic glandular morphology.en
dc.description.affiliationState Univ Campinas UNICAMP, Inst Biol, Dept Struct & Funct Biol, Sao Paulo, Brazil
dc.description.affiliationFed Univ Goias UFG, Inst Biol Sci, Dept Morphol, Goiania, Go, Brazil
dc.description.affiliationUniv Estadual Paulista UNESP, Inst Biosci Humanities & Exact Sci IBILCE, Dept Biol, BR-15054000 Sao Paulo, Brazil
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Inst Biosci Humanities & Exact Sci IBILCE, Dept Biol, BR-15054000 Sao Paulo, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 08/11386-9
dc.description.sponsorshipIdCNPq: 301596/2011-5
dc.format.extent373-386
dc.identifierhttp://dx.doi.org/10.1111/iep.12050
dc.identifier.citationInternational Journal Of Experimental Pathology. Hoboken: Wiley-blackwell, v. 94, n. 6, p. 373-386, 2013.
dc.identifier.doi10.1111/iep.12050
dc.identifier.issn0959-9673
dc.identifier.lattes0947193347312157
dc.identifier.orcid0000-0002-0970-4288
dc.identifier.orcid0000-0002-3622-460X
dc.identifier.urihttp://hdl.handle.net/11449/112855
dc.identifier.wosWOS:000330130400003
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofInternational Journal of Experimental Pathology
dc.relation.ispartofjcr1.938
dc.relation.ispartofsjr0,712
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectcastrationen
dc.subjectgergil prostateen
dc.subjectProgesteroneen
dc.subjectpubertyen
dc.titleProgesterone as a morphological regulatory factor of the male and female gerbil prostateen
dc.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-Blackwell
unesp.author.lattes0947193347312157[3]
unesp.author.orcid0000-0002-0970-4288[4]
unesp.author.orcid0000-0002-4476-6046[2]
unesp.author.orcid0000-0002-3622-460X[3]
unesp.author.orcid0000-0002-3622-460X[3]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências Letras e Ciências Exatas, São José do Rio Pretopt

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