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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/112622
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dc.contributor.authorInhasz Kiss, Ana Carolina-
dc.contributor.authorWoodside, Barbara-
dc.contributor.authorSinzato, Yuri Karen-
dc.contributor.authorBernardi, Maria Martha-
dc.contributor.authorKempinas, Wilma De Grava-
dc.contributor.authorAnselmo-Franci, Janete Aparecida-
dc.contributor.authorDamasceno, Debora Cristina-
dc.date.accessioned2014-12-03T13:10:53Z-
dc.date.accessioned2016-10-25T20:11:37Z-
dc.date.available2014-12-03T13:10:53Z-
dc.date.available2016-10-25T20:11:37Z-
dc.date.issued2013-10-16-
dc.identifierhttp://dx.doi.org/10.1186/1758-5996-5-61-
dc.identifier.citationDiabetology & Metabolic Syndrome. London: Biomed Central Ltd, v. 5, 10 p., 2013.-
dc.identifier.issn1758-5996-
dc.identifier.urihttp://hdl.handle.net/11449/112622-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/112622-
dc.description.abstractBackground: Neonatal STZ treatment induces a state of mild hyperglycemia in adult rats that disrupts metabolism and maternal/fetal interactions. The aim of this study was investigate the effect of neonatal STZ treatment on the physical development, behavior, and reproductive function of female Wistar rats from infancy to adulthood.Methods: At birth, litters were assigned either to a Control (subcutaneous (s.c.) citrate buffer, n = 10) or STZ group, (streptozotocin (STZ) - 100 mg/kg-sc, n = 6). Blood glucose levels were measured on postnatal days (PND) 35, 84 and 120. In Experiment 1 body weight, length and the appearance of developmental milestones such as eye and vaginal opening were monitored. To assess the relative contribution of the initial and long term effects of STZ treatment this group was subdivided based on blood glucose levels recorded on PND 120: STZ hyperglycemic (between 120 and 300 mg/dl) and STZ normoglycemic (under 120 mg/dl). Behavioral activity was assessed in an open field on PND 21 and 75. In Experiment 2 estrous cyclicity, sexual behavior and circulating gonadotropin, ovarian steroid, and insulin levels were compared between control and STZ-hyperglycemic rats. In all measures the litter was the experimental unit. Parametric data were analyzed using one-way or, where appropriate, two-way ANOVA and significant effects were investigated using Tukey's post hoc test. Fisher's exact test was employed when data did not satisfy the assumption of normality e. g. presence of urine and fecal boli on the open field between groups. Statistical significance was set at p < 0.05 for all data.Results: As expected neonatal STZ treatment caused hyperglycemia and hypoinsulinemia in adulthood. STZ-treated pups also showed a temporary reduction in growth rate that probably reflected the early loss of circulating insulin. Hyperglycemic rats also exhibited a reduction in locomotor and exploratory behavior in the open field. Mild hyperglycemia did not impair gonadotropin levels or estrous cylicity but ovarian steroid concentrations were altered.Conclusions: In female Wistar rats, neonatal STZ treatment impairs growth in infancy and results in mild hyperglycemia/hypoinsulinemia in adulthood that is associated with changes in the response to a novel environment and altered ovarian steroid hormone levels.en
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent10-
dc.language.isoeng-
dc.publisherBiomed Central Ltd.-
dc.sourceWeb of Science-
dc.subjectMild diabetesen
dc.subjectStreptozotocinen
dc.subjectRaten
dc.subjectDevelopmenten
dc.subjectBehavioren
dc.subjectReproductive functionen
dc.titleNeonatally induced mild diabetes: influence on development, behavior and reproductive function of female Wistar ratsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionConcordia Univ-
dc.contributor.institutionUniversidade Federal do ABC (UFABC)-
dc.contributor.institutionUniv Paulista-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationSao Paulo State Univ, Botucatu Biosci Inst, Dept Physiol, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationSao Paulo State Univ Unesp, Botucatu Med Sch, Dept Gynecol & Obstet, Lab Expt Res Gynecol & Obstet, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationConcordia Univ, Dept Psychol, Ctr Studies Behav Neurobiol, Montreal, PQ H4B 1R6, Canada-
dc.description.affiliationFed Univ ABC, Math Computat & Cognit Ctr, BR-09210580 Sao Paulo, Brazil-
dc.description.affiliationUniv Paulista, Grad Program Environm & Expt Pathol, Sao Paulo, Brazil-
dc.description.affiliationUniv Paulista, Grad Program Dent, Sao Paulo, Brazil-
dc.description.affiliationSao Paulo State Univ, Botucatu Biosci Inst, Dept Morphol, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationUniv Sao Paulo, Fac Odontol Ribeirao Preto, Dept Morfol Estomatol & Fisiol, Lab Neuroendocrinol Repdroducao, BR-14040904 Sao Paulo, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Botucatu Biosci Inst, Dept Physiol, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationUnespSao Paulo State Univ Unesp, Botucatu Med Sch, Dept Gynecol & Obstet, Lab Expt Res Gynecol & Obstet, BR-18618970 Sao Paulo, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Botucatu Biosci Inst, Dept Morphol, BR-18618970 Sao Paulo, Brazil-
dc.identifier.doi10.1186/1758-5996-5-61-
dc.identifier.wosWOS:000326633000001-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000326633000001.pdf-
dc.relation.ispartofDiabetology & Metabolic Syndrome-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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