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Pamidronate attenuates diastolic dysfunction induced by myocardial infarction associated with changes in geometric patterning

dc.contributor.authorGonçalves, Andrea de Freitas [UNESP]
dc.contributor.authorCongio, Luiz Henrique [UNESP]
dc.contributor.authorSantos, Priscila Portugal dos [UNESP]
dc.contributor.authorRafacho, Bruna Paola Murino [UNESP]
dc.contributor.authorPereira, Bruna Letícia Buzati [UNESP]
dc.contributor.authorClaro, Renan Floret Turini [UNESP]
dc.contributor.authorCosta, Nara Aline [UNESP]
dc.contributor.authorChiuso-Minicucci, Fernanda [UNESP]
dc.contributor.authorAzevedo, Paula Schmidt [UNESP]
dc.contributor.authorPolegato, Bertha Furlan [UNESP]
dc.contributor.authorOkoshi, Katashi [UNESP]
dc.contributor.authorPereira, Elenize Jamas [UNESP]
dc.contributor.authorOkoshi, Marina Politi [UNESP]
dc.contributor.authorPaiva, Sergio Alberto Rupp de [UNESP]
dc.contributor.authorZornoff, Leonardo Antonio Mamede [UNESP]
dc.contributor.authorMinicucci, Marcos Ferreira [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-10-21T13:08:55Z
dc.date.available2015-10-21T13:08:55Z
dc.date.issued2015-01-01
dc.description.abstractBackground/Aims: The aim of this study was to evaluate the influence of pamidronate on ventricular remodeling after myocardial infarction. Methods: Male Wistar rats were assigned to four groups: a sham group, in which animals were submitted to simulated surgery and received weekly subcutaneous injection of saline (S group; n=14); a group in which animals received weekly subcutaneous injection of pamidronate (3 mg/kg of body weight) and were submitted to simulated surgery (SP group, n=14); a myocardial infarction group, in which animals were submitted to coronary artery ligation and received weekly subcutaneous injection of saline (MI group, n=13); and a myocardial infarction group with pamidronate treatment (MIP group, n=14). The rats were observed for three months. Results: Animals submitted to MI had left chamber enlargement and worse diastolic and systolic function compared with SHAM groups. E/A ratio, LV posterior and relative wall thickness were lower in the MIP compared with the MI group. There was no interaction between pamidronate administration and MI on systolic function, myocyte hypertrophy, collagen content, and calcium handling proteins. Conclusion: Pamidronate attenuates diastolic dysfunction following MI.en
dc.description.affiliationUnespUniversidade Estadual Paulista, Departamento de Clínica Médica, Faculdade de Medicina de Botucatu
dc.description.affiliationUnespUniversidade Estadual Paulista, Departamento de Microbiologia e Imunologia, Instituto de Biociências de Botucatu
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2011/10328-8
dc.format.extent259-269
dc.identifierhttp://www.karger.com/Article/FullText/369693
dc.identifier.citationCellular Physiology And Biochemistry. Basel: Karger, v. 35, n. 1, p. 259-269, 2015.
dc.identifier.doi10.1159/000369693
dc.identifier.fileWOS000348048000024.pdf
dc.identifier.issn1015-8987
dc.identifier.lattes1590971576309420
dc.identifier.lattes4463138671998432
dc.identifier.lattes5016839015394547
dc.identifier.lattes1213140801402647
dc.identifier.lattes7438704034471673
dc.identifier.orcid0000-0002-5843-6232
dc.identifier.urihttp://hdl.handle.net/11449/128313
dc.identifier.wosWOS:000348048000024
dc.language.isoeng
dc.publisherKarger
dc.relation.ispartofCellular Physiology And Biochemistry
dc.relation.ispartofjcr5.500
dc.relation.ispartofsjr1,561
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectVentricular remodelingen
dc.subjectBisphosphonatesen
dc.subjectCalcium handling proteinsen
dc.titlePamidronate attenuates diastolic dysfunction induced by myocardial infarction associated with changes in geometric patterningen
dc.typeArtigo
dcterms.licensehttp://www.karger.com/Services/RightsPermissions
dcterms.rightsHolderKarger
dspace.entity.typePublication
unesp.author.lattes5016839015394547[15]
unesp.author.lattes1590971576309420
unesp.author.lattes4463138671998432
unesp.author.lattes1213140801402647[9]
unesp.author.lattes7438704034471673
unesp.author.lattes4563764623232492[10]
unesp.author.orcid0000-0002-5980-4367[16]
unesp.author.orcid0000-0002-2875-9532[10]
unesp.author.orcid0000-0001-8980-8839[13]
unesp.author.orcid0000-0003-4412-1990[14]
unesp.author.orcid0000-0002-5843-6232[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt
unesp.departmentMicrobiologia e Imunologia - IBBpt

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