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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/70607
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dc.contributor.authorSoares de Alencar Mota, Clécia-
dc.contributor.authorRibeiro, Carla-
dc.contributor.authorde Araújo, Gustavo Gomes-
dc.contributor.authorde Araújo, Michel Barbosa-
dc.contributor.authorde Barros Manchado-Gobatto, Fúlvia-
dc.contributor.authorVoltarelli, Fabrício Azevedo-
dc.contributor.authorde Oliveira, Camila Aparecida Machado-
dc.contributor.authorLuciano, Eliete-
dc.contributor.authorde Mello, Maria Alice Rostom-
dc.date.accessioned2014-05-27T11:23:41Z-
dc.date.accessioned2016-10-25T18:26:04Z-
dc.date.available2014-05-27T11:23:41Z-
dc.date.available2016-10-25T18:26:04Z-
dc.date.issued2008-10-02-
dc.identifierhttp://dx.doi.org/10.1186/1472-6823-8-11-
dc.identifier.citationBMC Endocrine Disorders, v. 8.-
dc.identifier.issn1472-6823-
dc.identifier.urihttp://hdl.handle.net/11449/70607-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/70607-
dc.description.abstractBackground: Ninety percent of cases of diabetes are of the slowly evolving non-insulin-dependent type, or Type 2 diabetes. Lack of exercise is regarded as one of the main causes of this disorder. In this study we analyzed the effects of physical exercise on glucose homeostasis in adult rats with type 2 diabetes induced by a neonatal injection of alloxan. Methods: Female Wistar rats aged 6 days were injected with either 250 mg/ kg of body weight of alloxan or citrate buffer 0.01 M (controls). After weaning, half of the animals in each group were subjected to physical training adjusted to meet the aerobic-anaerobic metabolic transition by swimming 1 h/day for 5 days a week with weight overloads. The necessary overload used was set and periodically readjusted for each rat through effort tests based on the maximal lactate steady state procedure. When aged 28, 60, 90, and 120 days, the rats underwent glucose tolerance tests (GTT) and their peripheral insulin sensitivity was evaluated using the HOMA index. Results: The area under the serum glucose curve obtained through GTT was always higher in alloxan-treated animals than in controls. A decrease in this area was observed in trained alloxan-treated rats at 90 and 120 days old compared with non-trained animals. At 90 days old the trained controls showed lower HOMA indices than the non-trained controls. Conclusion: Neonatal administration of alloxan induced a persistent glucose intolerance in all injected rats, which was successfully counteracted by physical training in the aerobic/anaerobic metabolic transition. © 2008 Mota et al; licensee BioMed Central Ltd.en
dc.language.isoeng-
dc.sourceScopus-
dc.subjectalloxan-
dc.subjectglucose-
dc.subjectlactic acid-
dc.subjectaerobic metabolism-
dc.subjectalloxan diabetes mellitus-
dc.subjectanaerobic metabolism-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectcontrolled study-
dc.subjectfemale-
dc.subjectglucose blood level-
dc.subjectglucose homeostasis-
dc.subjectglucose intolerance-
dc.subjectglucose tolerance test-
dc.subjectinsulin sensitivity-
dc.subjectkinesiotherapy-
dc.subjectlactate blood level-
dc.subjectnon insulin dependent diabetes mellitus-
dc.subjectnonhuman-
dc.subjectphysical activity-
dc.subjectrat-
dc.subjectsteady state-
dc.subjectswimming-
dc.subjectWistar rat-
dc.titleExercise training in the aerobic/anaerobic metabolic transition prevents glucose intolerance in alloxan-treated ratsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.description.affiliationInstitute of Biosciences Department of Physical Education São Paulo State University, Unesp, SP-
dc.description.affiliationInstitute of Biosciences Department of Physiology and Biophysical Campinas State University, Unicamp, SP-
dc.description.affiliationUnespInstitute of Biosciences Department of Physical Education São Paulo State University, Unesp, SP-
dc.identifier.doi10.1186/1472-6823-8-11-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-54049150824.pdf-
dc.relation.ispartofBMC Endocrine Disorders-
dc.identifier.scopus2-s2.0-54049150824-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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