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dc.contributor.authorGobbo, Marina Guimaraes [UNESP]
dc.contributor.authorTaboga, Sebastiao Roberto [UNESP]
dc.contributor.authorRibeiro, Daniele Lisboa [UNESP]
dc.contributor.authorGoes, Rejane Maira [UNESP]
dc.date.accessioned2014-05-20T14:00:56Z
dc.date.available2014-05-20T14:00:56Z
dc.date.issued2012-02-01
dc.identifierhttp://dx.doi.org/10.1016/j.micron.2011.09.009
dc.identifier.citationMicron. Oxford: Pergamon-Elsevier B.V. Ltd, v. 43, n. 2-3, p. 326-333, 2012.
dc.identifier.issn0968-4328
dc.identifier.urihttp://hdl.handle.net/11449/21532
dc.description.abstractThe stromal microenvironment is pivotal to prostate physiology and malign transformation. Diabetes leads to testosterone withdrawal and affects the prostate stromal compartment and smooth muscle cells in a similar way to that observed after castration. However the response of these cells and their involvement in extracellular matrix remodeling is not satisfactorily understood. We investigated the changes caused in the short term (one week) by alloxan-induced diabetes in the stromal components of the rat ventral prostate (VP) with an emphasis on morphological alterations of stromal cells, their conversion to a myofibroblast phenotype and the remodeling of extracellular matrix and the influence of insulin therapy. Adult male Wistar rats were assigned into untreated diabetic (n = 12), insulin-treated (n = 8) diabetic and control (n = 10) groups. Diabetes was induced by means of the injection of alloxan (40 mg/kg b.w.), while the control animals received saline solution only. Insulin (5 UI) was administered daily for one week after diabetes diagnosis. Testosterone and estrogen plasma levels were determined. VP was analyzed using transmission electron microscopy. The main stromal cells were identified by means of light microscopy, using immunocytochemistry for specific markers - vimentin for fibroblasts, a-actin for smooth muscle cells (smc) and vimentin/calponin for myofibroblasts, following the estimation of their relative frequency and absolute volume by means of stereology. After one week diabetes led to a marked decrease in testosterone levels and an atrophy of about 35% in the VP. The relative frequency of smc and collagen fibers increased in the VP of diabetic rats but their absolute weight remained unchanged. Experimental diabetes promptly altered smc morphology which assumed at the ultrastructural level a shrunken appearance with the approximation of cytoplasmic dense bodies and also exhibited a decreased immunoreactivity to calponin. The conversion of stromal cells to a myofibroblast phenotype did not occur in alloxan-induced diabetes, as evaluated by double immunoreaction to calponin and vimentin. Insulin treatment maintained testosterone levels and preserved at least partly the cell morphology and collagen fiber organization of the prostate stroma in short-term diabetes. The apparent collagen increase observed by means of microscopic analysis in the stromal prostate compartment in the short term after diabetes is mainly associated with gland atrophy and does not involve the formation of new collagen fibers, the generation of myofibroblast-like cells or the acquisition of a secretory phenotype by stromal cells. (C) 2011 Elsevier Ltd. All rights reserved.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent326-333
dc.language.isoeng
dc.publisherPergamon-Elsevier B.V. Ltd
dc.relation.ispartofMicron
dc.sourceWeb of Science
dc.subjectAlloxan-induced diabetesen
dc.subjectVentral prostateen
dc.subjectStromal remodelingen
dc.subjectSmooth muscle cellsen
dc.subjectInsulinen
dc.titleShort-term stromal alterations in the rat ventral prostate following alloxan-induced diabetes and the influence of insulin replacementen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderPergamon-Elsevier B.V. Ltd
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.description.affiliationUNESP Univ Estadual Paulista, Dept Biol, IBILCE Inst Biosci, Sao Jose do Rio Preto, SP, Brazil
dc.description.affiliationUniversidade Federal de Uberlândia (UFU), Histol Sect, Inst Biomed Sci, BR-38400 Uberlandia, MG, Brazil
dc.description.affiliationUnespUNESP Univ Estadual Paulista, Dept Biol, IBILCE Inst Biosci, Sao Jose do Rio Preto, SP, Brazil
dc.identifier.doi10.1016/j.micron.2011.09.009
dc.identifier.wosWOS:000299605300032
dc.rights.accessRightsAcesso restrito
dc.description.sponsorshipIdCNPq: 302693/2008-4
dc.description.sponsorshipIdFAPESP: 06/07008-3
dc.description.sponsorshipIdFAPESP: 07/04252-3
dc.description.sponsorshipIdFAPESP: 08/00542-0
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências Letras e Ciências Exatas, São José do Rio Pretopt
dc.identifier.lattes1445259468526188
dc.identifier.lattes0947193347312157
dc.identifier.orcid0000-0002-0970-4288
dc.identifier.orcid0000-0002-3622-460X
unesp.author.lattes1445259468526188
unesp.author.lattes0947193347312157[4]
unesp.author.orcid0000-0002-0970-4288[2]
unesp.author.orcid0000-0002-3622-460X[4]
dc.relation.ispartofjcr1.728
dc.relation.ispartofsjr0,624
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