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Euterpe oleracea mart. (açaí) reduces oxidative stress and improves energetic metabolism in myocardial ischemia-reperfusion injury in rats

dc.contributor.authorAlegre, Patricia [UNESP]
dc.contributor.authorMathias, Livia [UNESP]
dc.contributor.authorLourenço, Maria Angelica [UNESP]
dc.contributor.authorDos Santos, Priscila Portugal [UNESP]
dc.contributor.authorGonçalves, Andrea [UNESP]
dc.contributor.authorFernandes, Ana Angélica [UNESP]
dc.contributor.authorGaiolla, Paula Schmidt Azevedo [UNESP]
dc.contributor.authorMinicucci, Marcos Ferreira [UNESP]
dc.contributor.authorZornoff, Leonardo [UNESP]
dc.contributor.authorPaiva, Sergio Alberto Rupp [UNESP]
dc.contributor.authorPolegato, Bertha Furlan [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-12T02:35:34Z
dc.date.available2020-12-12T02:35:34Z
dc.date.issued2020-01-01
dc.description.abstractBackground: Euterpe oleracea Mart. (açaí) is a fruit with high antioxidant capacity and could be an adjuvant strategy to attenuate ischemia-reperfusion injury. Objective: To evaluate the influence of açaí in global ischemia-reperfusion model in rats. Methods: Wistar rats were assigned to 2 groups: Control (C: receiving standard chow; n = 9) and Açaí (A: receiving standard chow supplemented with 5% açaí; n = 10). After six weeks, the animals were subjected to the global ischemia-reperfusion protocol and an isolated heart study to evaluate left ventricular function. Level of significance adopted: 5%. Results: There was no difference between the groups in initial body weight, final body weight and daily feed intake. Group A presented lower lipid hydroperoxide myocardial concentration and higher catalase activity, superoxide dismutase and glutathione peroxidase than group C. We also observed increased myocardial activity of β-hydroxyacyl coenzyme-A dehydrogenase, pyruvate dehydrogenase, citrate synthase, complex I, complex II and ATP synthase in the A group as well as lower activity of the lactate dehydrogenase and phosphofructokinase enzymes. The systolic function was similar between the groups, and the A group presented poorer diastolic function than the C group. We did not observe any difference between the groups in relation to myocardial infarction area, total and phosphorylated NF-κB, total and acetylated FOXO1, SIRT1 and Nrf-2 protein expression. Conclusion: despite improving energy metabolism and attenuating oxidative stress, açai supplementation did not decrease the infarcted area or improve left ventricular function in the global ischemia-reperfusion model. (Arq Bras Cardiol. 2020; 114(1):78-86).en
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho-UNESP
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho-UNESP
dc.format.extent78-86
dc.identifierhttp://dx.doi.org/10.36660/abc.20180140
dc.identifier.citationArquivos Brasileiros de Cardiologia, v. 114, n. 1, p. 78-86, 2020.
dc.identifier.doi10.36660/abc.20180140
dc.identifier.fileS0066-782X2020000100078.pdf
dc.identifier.issn1678-4170
dc.identifier.issn0066-782X
dc.identifier.lattes1213140801402647
dc.identifier.orcid0000-0002-5843-6232
dc.identifier.scieloS0066-782X2020000100078
dc.identifier.scopus2-s2.0-85079321765
dc.identifier.urihttp://hdl.handle.net/11449/201552
dc.language.isoeng
dc.language.isopor
dc.relation.ispartofArquivos Brasileiros de Cardiologia
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectChemical Reactions
dc.subjectEnergy Metabolism
dc.subjectEuterpe Olerácea
dc.subjectMyocardial Ischemia
dc.subjectMyocardial Reperfusion Injury
dc.subjectOxidative Stress
dc.subjectRats
dc.titleEuterpe oleracea mart. (açaí) reduces oxidative stress and improves energetic metabolism in myocardial ischemia-reperfusion injury in ratsen
dc.titleEuterpe Oleracea Mart. (Açaí) reduz o estresse oxidativo e melhora o metabolismo energético da lesão de isquemia-reperfusão miocárdica em ratospt
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes4563764623232492[11]
unesp.author.lattes1213140801402647[6]
unesp.author.orcid0000-0003-1159-5030[4]
unesp.author.orcid0000-0002-5980-4367[8]
unesp.author.orcid0000-0002-9831-8820[9]
unesp.author.orcid0000-0003-4412-1990[10]
unesp.author.orcid0000-0002-2875-9532[11]
unesp.author.orcid0000-0002-5843-6232[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentClínica Médica - FMBpt
unesp.departmentDiagnóstico e Cirurgia - FOARpt

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