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Dietary restriction: Metabolic shifting for cardiac health

dc.contributor.authorFaine, L. A.
dc.contributor.authorCicogna, A. C.
dc.contributor.authorDiniz, Y. S.
dc.contributor.authorAlmeida, J. A.
dc.contributor.authorBurneiko, R. C.
dc.contributor.authorRodrigues, H. G.
dc.contributor.authorNovelli, E. L. B.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:20:37Z
dc.date.available2014-05-27T11:20:37Z
dc.date.issued2003-03-01
dc.description.abstractPurpose: To determine the effect of dietary restriction on metabolic pathways and the relationship of the metabolic shifting on antioxidant enzymes in cardiac tissue. Design: Randomized, controlled study. Male rats at 60 days old were randomly divided into four groups. Materials and Methods: The rats of control groups C30 and C60 were given free access to the diet over 30 and 60 days. The rats of the DR30 group were fed 60% of the chow consumed by the control groups over 30 days. The animals of the DR60 group ate 60% of the amount consumed by the C60 group over 60 days. Serum was used for total protein, lactate dehydrogenase (LDH), alanine aminotransferase (ALT) and aspartate aminotransferase (AST). Protein, glycogen, total lipids, superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), LDH, AST and ALT were determined in cardiac tissue. Results: Dietary restriction induced diminished serum and cardiac LDH activities. AST activities were lower in the serum and cardiac muscle of the DR60 animals. Dietary restriction induced elevated total lipid concentrations in cardiac muscle. No significant differences were observed in total protein and glycogen content among the groups. Antioxidant enzyme determinations demonstrated increased cardiac GSH-Px activities in the DR60 animals and increased SOD activities in the cardiac tissue of both feed-restricted groups. Conclusions: Dietary restriction was protective against oxidative stress in the heart by improving cardiac endogenous antioxidant defences and shifting the metabolic pathway for energy production.en
dc.description.affiliationPost Graduation Course Institute of Biological Science University Estadual Paulista, Botucatu, São Paulo
dc.description.affiliationDepartment of Clinical Cardiology Institute of Biological Science University Estadual Paulista, Botucatu, São Paulo
dc.description.affiliationDept. of Chemistry and Biochemistry Institute of Biological Science University Estadual Paulista, Botucatu, São Paulo
dc.format.extent23-29
dc.identifierhttp://dx.doi.org/10.1080/135908403100009501
dc.identifier.citationJournal of Nutritional and Environmental Medicine, v. 13, n. 1, p. 23-29, 2003.
dc.identifier.doi10.1080/135908403100009501
dc.identifier.issn1359-0847
dc.identifier.scopus2-s2.0-0038520986
dc.identifier.urihttp://hdl.handle.net/11449/67202
dc.language.isoeng
dc.relation.ispartofJournal of Nutritional and Environmental Medicine
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectCardiac health
dc.subjectDietary restriction
dc.subjectMetabolism
dc.subjectOxidative stress
dc.subjectantioxidant
dc.subjectenzyme
dc.subjectglutathione peroxidase
dc.subjectglycogen
dc.subjectplasma protein
dc.subjectprotein
dc.subjectsuperoxide dismutase
dc.subjectalanine aminotransferase blood level
dc.subjectanimal experiment
dc.subjectaspartate aminotransferase blood level
dc.subjectclinical pathway
dc.subjectcontrolled study
dc.subjectdiet restriction
dc.subjecteating
dc.subjectenzyme activity
dc.subjectfood intake
dc.subjecthealth
dc.subjectheart
dc.subjectheart function
dc.subjectheart muscle
dc.subjectlactate dehydrogenase blood level
dc.subjectlipid blood level
dc.subjectlipid metabolism
dc.subjectmetabolism
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectrat
dc.subjectAnimalia
dc.titleDietary restriction: Metabolic shifting for cardiac healthen
dc.typeArtigo
dcterms.licensehttp://informahealthcare.com/userimages/ContentEditor/1255620309227/Copyright_And_Permissions.pdf
dspace.entity.typePublication
unesp.author.lattes9418970103564137[2]
unesp.author.orcid0000-0002-4402-6523[2]

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