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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/68768
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dc.contributor.authorZornoff, Leonardo Antonio Mamede-
dc.contributor.authorMatsubara, Beatriz Bojikian-
dc.contributor.authorMatsubara, Luiz Shiguero-
dc.contributor.authorGaiolla, Paula Schmidt Azevedo-
dc.contributor.authorMinicucci, Marcos Ferreira-
dc.contributor.authorCampana, Alvaro O.-
dc.contributor.authorPaiva, Sergio Alberto Rupp de-
dc.date.accessioned2014-05-27T11:21:48Z-
dc.date.accessioned2016-10-25T18:21:55Z-
dc.date.available2014-05-27T11:21:48Z-
dc.date.available2016-10-25T18:21:55Z-
dc.date.issued2006-02-01-
dc.identifierhttp://dx.doi.org/10.1016/j.nut.2005.05.008-
dc.identifier.citationNutrition, v. 22, n. 2, p. 146-151, 2006.-
dc.identifier.issn0899-9007-
dc.identifier.urihttp://hdl.handle.net/11449/68768-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68768-
dc.description.abstractObjective: We studied the effects of β-carotene (BC) on ventricular remodeling after myocardial infarction. Methods: Myocardial infarction was induced in Wistar rats that were then treated with a BC diet (500 mg/kg of diet per day; MI-BC; n = 27) or a regular diet (MI; n = 27). Hearts were analyzed in vivo and in vitro after 6 mo. Results: BC caused decreased left ventricular wall thickness (MI = 1.49 ± 0.3 mm, MI-BC = 1.23 ± 0.2 mm, P = 0.027) and increased diastolic (MI = 0.83 ± 0.15 cm2, MI-BC = 0.98 ± 0.14 cm2, P = 0.020) and systolic (MI = 0.56 ± 0.12 cm2, MI-BC = 0.75 ± 0.13 cm2, P = 0.002) left ventricular chamber areas. With respect to systolic function, the BC group presented less change in fractional area than did controls (MI = 32.35 ± 6.67, MI-BC = 23.77 ± 6.06, P = 0.004). There was no difference in transmitral diastolic flow velocities between groups. In vitro results showed decreased maximal isovolumetric systolic pressure (MI = 125.5 ± 24.1 mmHg, MI-BC = 95.2 ± 28.4 mmHg, P = 0.019) and increased interstitial myocardial collagen concentration (MI = 3.3 ± 1.2%, MI-BC = 5.8 ± 1.7%, P = 0.004) in BC-treated animals. Infarct sizes were similar between groups (MI = 45.0 ± 6.6%, MI-BC = 48.0 ± 5.8%, P = 0.246). Conclusion: Taken together, these data suggest that BC has adverse effects on ventricular remodeling after myocardial infarction. © 2006 Elsevier Inc. All rights reserved.en
dc.format.extent146-151-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAntioxidants-
dc.subjectFibrosis-
dc.subjectHypertrophy-
dc.subjectMyocardial function-
dc.subjectVentricular dilation-
dc.subjectbeta carotene-
dc.subjectacute heart infarction-
dc.subjectanimal experiment-
dc.subjectanimal tissue-
dc.subjectchromatography-
dc.subjectcontrolled study-
dc.subjectdiastolic blood pressure-
dc.subjectheart ventricle remodeling-
dc.subjectin vitro study-
dc.subjectin vivo study-
dc.subjectmale-
dc.subjectmorphometrics-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectrat-
dc.subjectsystolic blood pressure-
dc.subjectvitamin supplementation-
dc.subjectAnimals-
dc.subjectbeta Carotene-
dc.subjectDietary Supplements-
dc.subjectHeart-
dc.subjectMale-
dc.subjectMyocardial Infarction-
dc.subjectMyocardium-
dc.subjectRandom Allocation-
dc.subjectRats-
dc.subjectRats, Wistar-
dc.subjectTreatment Outcome-
dc.subjectVentricular Function-
dc.subjectVentricular Remodeling-
dc.subjectAnimalia-
dc.subjectRattus norvegicus-
dc.titleβ-Carotene supplementation results in adverse ventricular remodeling after acute myocardial infarctionen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationFaculdade de Medicina Departamento de Clinia Medica, Botucatu, Sao Paulo-
dc.identifier.doi10.1016/j.nut.2005.05.008-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofNutrition-
dc.identifier.scopus2-s2.0-31944439684-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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