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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/67578
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dc.contributor.authorPrada, F. J A-
dc.contributor.authorMacedo, D. V.-
dc.contributor.authorDe Mello, Maria Alice Rostom-
dc.date.accessioned2014-05-27T11:21:00Z-
dc.date.accessioned2016-10-25T18:19:14Z-
dc.date.available2014-05-27T11:21:00Z-
dc.date.available2016-10-25T18:19:14Z-
dc.date.issued2003-12-01-
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/15686121-
dc.identifier.citationResearch Communications in Molecular Pathology and Pharmacology, v. 113-114, p. 213-228.-
dc.identifier.issn1078-0297-
dc.identifier.urihttp://hdl.handle.net/11449/67578-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/67578-
dc.description.abstractProtein malnutrition leads to functional impairment in several organs, which is not fully restored with nutritional recovery. Little is known about the role of oxidative stress in the genesis of these alterations. This study was designed to assess the sensitivity of blood oxidative stress biomarkers to a dietary protein restriction. Male Wistar rats were divided into two groups, according to the diet fed from weaning (21 days) to 60 day old: normal protein (17% protein) and low protein (6% protein). Serum protein, albumin, free fatty acid and liver glycogen and lipids were evaluated to assess the nutritional status. Blood glutathione reductase (GR) and catalase (CAT) activities, plasma total sulfhydryl groups concentration (TSG) as well as plasma thiobarbituric acid reactive substances (TBARs) and reactive carbonyl derivatives (RCD) were measured as biomarkers of the antioxidant system and oxidative damage, respectively. The glucose metabolism in soleus muscle was also evaluated as an index of stress severity imposed to muscular mass by protein malnutrition. No difference was observed in muscle glucose metabolism or plasma RCD concentration between both groups. However, our results showed that the low protein group had higher plasma TBARs (62%) concentration and lower TSG (44%) concentration than control group, indicating increased reactive oxygen species production in low protein group. The enhancement of erythrocyte GR (29%) and CAT (28%) activities in this group also suggest an adaptation to the stress generated by the protein deficiency. Taken together, the results presented here show that the biomarkers used were able to reflect the oxidative stress level induced by this specific protein deficient diet.en
dc.format.extent213-228-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAdaptation to stress-
dc.subjectBlood catalase-
dc.subjectBlood glutathione reductase-
dc.subjectNutritional recovery-
dc.subjectOxidative stress-
dc.subjectProtein malnutrition-
dc.subjectStress generated by protein deficiency-
dc.subjectSulfhydryl groups-
dc.subjectTBARs-
dc.subjectWistar rats-
dc.subjectantioxidant-
dc.subjectbiological marker-
dc.subjectcarbonyl derivative-
dc.subjectcatalase-
dc.subjectfatty acid-
dc.subjectglutathione reductase-
dc.subjectreactive oxygen metabolite-
dc.subjectthiobarbituric acid-
dc.subjectthiobarbituric acid derivative-
dc.subjectthiol derivative-
dc.subjectadaptation-
dc.subjectalbumin blood level-
dc.subjectanimal experiment-
dc.subjectcontrolled study-
dc.subjectglucose metabolism-
dc.subjectmale-
dc.subjectmuscle mass-
dc.subjectnonhuman-
dc.subjectnutritional status-
dc.subjectoxidative stress-
dc.subjectpriority journal-
dc.subjectprotein blood level-
dc.subjectprotein deficiency-
dc.subjectprotein malnutrition-
dc.subjectprotein restriction-
dc.subjectrat-
dc.subjectrat strain-
dc.subjectsoleus muscle-
dc.subjectweaning-
dc.subjectAdaptation, Physiological-
dc.subjectAnimals-
dc.subjectBiological Markers-
dc.subjectCatalase-
dc.subjectGlucose-
dc.subjectGlutathione Reductase-
dc.subjectMale-
dc.subjectNutritional Status-
dc.subjectOxidative Stress-
dc.subjectProtein Deficiency-
dc.subjectRats-
dc.subjectRats, Wistar-
dc.subjectSulfhydryl Compounds-
dc.subjectThiobarbituric Acid Reactive Substances-
dc.titleEvaluation of a protein deficient diet in rats through blood oxidative stress biomarkersen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv. de Campinas (UNICAMP/SP) Lab. Bioquim. Exercicio (Labex)-
dc.description.affiliationUniv. Estadual Paulista (UNESP/RC) Depto. de Educacao Fisica-
dc.description.affiliationDepartamento de Educacao Fisica IB - UNESP, Av. 24-A, 1515, 13506-900 - Rio Claro/SP-
dc.description.affiliationUnespUniv. Estadual Paulista (UNESP/RC) Depto. de Educacao Fisica-
dc.description.affiliationUnespDepartamento de Educacao Fisica IB - UNESP, Av. 24-A, 1515, 13506-900 - Rio Claro/SP-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofResearch Communications in Molecular Pathology and Pharmacology-
dc.identifier.scopus2-s2.0-13144258737-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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