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Effects of maternal diabetes on male offspring: high cell proliferation and increased activity of MMP-2 in the ventral prostate

dc.contributor.authorDamasceno, A. A.
dc.contributor.authorCarvalho, C. P.
dc.contributor.authorSantos, E. M. B.
dc.contributor.authorBotelho, F. V.
dc.contributor.authorAraujo, F. A.
dc.contributor.authorDeconte, S. R.
dc.contributor.authorTomiosso, T. C.
dc.contributor.authorBalbi, A. P. C.
dc.contributor.authorZanon, R. G.
dc.contributor.authorTaboga, S. R. [UNESP]
dc.contributor.authorGoes, R. M. [UNESP]
dc.contributor.authorRibeiro, D. L.
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-03-18T15:52:59Z
dc.date.available2015-03-18T15:52:59Z
dc.date.issued2014-10-01
dc.description.abstractThis study presents a comprehensive view of the histological and functional status of the prostate of adult rat offspring of mothers subjected to gestational diabetes induced by alloxan. The ventral prostate of male adult offspring of diabetic (DP) or normal (CP) mothers was evaluated for collagen fibres, cell death, fibroblasts, smooth muscle cells, cell proliferation, matrix metalloproteinases (MMPs), androgen receptors (AR), transforming growth factor beta 1 (TGF beta-1), catalase and total antioxidant activity. The prostates of DP animals were lower in weight than those of the CP group. The DP group also exhibited hyperglycaemia and hypotestosteronemia, higher cell proliferation and AR expression, a reduction in alpha-actin (possibly interfering with the reproductive function of the prostate), and enhanced activity of MMP-2, although the absolute content of MMP-2 was lower in this group. These findings were associated with increased TGF beta-1 and decreased collagen distribution. The prostates of DP rats additionally exhibited reductions in catalase and total antioxidant activity. Thus, rats developing in a diabetic intrauterine environment have glycaemic and hormonal changes that impact on the structure and physiology of the prostate in adulthood. The increased AR expression possibly leads to elevated cell proliferation. Stromal remodelling was characterized by enhanced activity of MMP-2 and collagen degradation, even with increased TGF beta-1 activation. These changes associated with increased oxidative stress might interfere with tissue architecture and glandular homeostasis.en
dc.description.affiliationUniv Fed Uberlandia, Inst Biomed Sci ICBIM, Histol Sect, BR-38400 Uberlandia, MG, Brazil
dc.description.affiliationUniv Fed Uberlandia, Inst Genet & Biochem INGEB, BR-38400 Uberlandia, MG, Brazil
dc.description.affiliationUniv Fed Uberlandia, Inst Biomed Sci ICBIM, Physiol Sect, BR-38400 Uberlandia, MG, Brazil
dc.description.affiliationUniv Fed Uberlandia, Inst Biomed Sci ICBIM, Anat Sect, BR-38400 Uberlandia, MG, Brazil
dc.description.affiliationUniv Estadual Paulista, Dept Biol, Inst Biosci Letters & Exact Sci IBILCE, Paulista, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Dept Biol, Inst Biosci Letters & Exact Sci IBILCE, Paulista, Brazil
dc.format.extent257-269
dc.identifierhttp://dx.doi.org/10.1007/s00441-014-1941-6
dc.identifier.citationCell And Tissue Research. New York: Springer, v. 358, n. 1, p. 257-269, 2014.
dc.identifier.doi10.1007/s00441-014-1941-6
dc.identifier.issn0302-766X
dc.identifier.lattes1445259468526188
dc.identifier.lattes0947193347312157
dc.identifier.orcid0000-0002-0970-4288
dc.identifier.orcid0000-0002-3622-460X
dc.identifier.urihttp://hdl.handle.net/11449/116267
dc.identifier.wosWOS:000343044300022
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofCell And Tissue Research
dc.relation.ispartofjcr3.043
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectMaternal diabetesen
dc.subjectProstateen
dc.subjectCell proliferationen
dc.subjectMetalloproteinaseen
dc.subjectAndrogen receptoren
dc.subjectRat (Wistar)en
dc.titleEffects of maternal diabetes on male offspring: high cell proliferation and increased activity of MMP-2 in the ventral prostateen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
unesp.author.lattes1445259468526188
unesp.author.lattes0947193347312157[11]
unesp.author.orcid0000-0002-0970-4288[10]
unesp.author.orcid0000-0002-3622-460X[11]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentBiologia - IBILCEpt

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