dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:50:53Z
dc.date.accessioned2022-10-05T14:24:07Z
dc.date.available2014-05-20T13:50:53Z
dc.date.available2022-10-05T14:24:07Z
dc.date.created2014-05-20T13:50:53Z
dc.date.issued2010-01-01
dc.identifierCellular Physiology and Biochemistry. Basel: Karger, v. 26, n. 3, p. 395-402, 2010.
dc.identifier1015-8987
dc.identifierhttp://hdl.handle.net/11449/18157
dc.identifier10.1159/000320563
dc.identifierWOS:000281236600015
dc.identifier6309835137998766
dc.identifier6990977122340795
dc.identifier5016839015394547
dc.identifier1213140801402647
dc.identifier7438704034471673
dc.identifier0000-0002-5843-6232
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3892650
dc.description.abstractBackground/Aims: Experimental studies suggest that vitamin A plays a role in regulating cardiac structure and function. We tested the hypothesis that cardiac vitamin A deficiency is associated with adverse myocardial remodeling in young adult rats. Methods: Two groups of young female rats, control (C - n = 29) and tissue vitamin A deficient (RVA - n = 31), were subjected to transthoracic echocardiography exam, isolated rat heart study and biochemical study. Results: The RVA rats showed a reduced total vitamin A concentration in both the liver and heart [vitamin A in heart, mu mol/kg (C = 0.95 +/- 0.44 and RVA = 0.24 +/- 0.16, p = 0.01)] with the same serum retinol levels (C = 0.73 +/- 0.29 mu mol/L e RVA = 0.62 +/- 0.17 mu mol/L, p = 0.34). The RVA rats showed higher left ventricular diameters and reduced systolic function. The RVA rats also demonstrated increased lipid hydroperoxide/total antioxidant capacity ratio and cardiac levels of IFN-gamma and TNF-alpha but not of metalloproteinase (MMP)-2 and -9 activity. on the other hand, the RVA rats had decreased levels of beta-hydroxyacylcoenzyme A dehydrogenase and lactate dehydrogenase. Conclusions: Tissue vitamin A deficiency stimulated cardiac remodeling and ventricular dysfunction. Additionally, the data support the involvement of oxidative stress, energy metabolism, and cytokine production in this remodeling process. Copyright (C) 2010 S. Karger AG, Basel
dc.languageeng
dc.publisherKarger
dc.relationCellular Physiology and Biochemistry
dc.relation5.500
dc.relation1,561
dc.rightsAcesso aberto
dc.sourceWeb of Science
dc.subjectInflammation
dc.subjectOxidative stress
dc.subjectEnergetic metabolism
dc.subjectVitamin A
dc.subjectRemodeling
dc.titleVentricular Remodeling Induced by Tissue Vitamin A Deficiency in Rats
dc.typeResumo


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