dc.contributorUniversidade Estadual de Campinas (UNICAMP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:21:00Z
dc.date.available2014-05-27T11:21:00Z
dc.date.created2014-05-27T11:21:00Z
dc.date.issued2003-12-01
dc.identifierResearch Communications in Molecular Pathology and Pharmacology, v. 113-114, p. 213-228.
dc.identifier1078-0297
dc.identifierhttp://hdl.handle.net/11449/67578
dc.identifier2-s2.0-13144258737
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.
dc.languageeng
dc.relationResearch Communications in Molecular Pathology and Pharmacology
dc.rightsAcesso restrito
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 biomarkers
dc.typeArtículos de revistas


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