Rutin administration attenuates myocardial dysfunction in diabetic rats

Detalhes bibliográficos
Autor(a) principal: Guimarães, Julliano F. C. [UNESP]
Data de Publicação: 2015
Outros Autores: Muzio, Bruno P. [UNESP], Rosa, Camila M. [UNESP], Nascimento, André F. [UNESP], Sugizaki, Mário M. [UNESP], Fernandes, Ana A. H. [UNESP], Cicogna, Antonio C. [UNESP], Padovani, Carlos R. [UNESP], Okoshi, Marina P. [UNESP], Okoshi, Katashi [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/s12933-015-0255-7
http://hdl.handle.net/11449/131093
Resumo: Oxidative stress plays a major role in diabetic cardiomyopathy pathogenesis. Anti-oxidant therapy has been investigated in preventing or treating several diabetic complications. However, anti-oxidant action on diabetic-induced cardiac remodeling is not completely clear. This study evaluated the effects of rutin, a flavonoid, on cardiac and myocardial function in diabetic rats. Wistar rats were assigned into control (C, n = 14); control-rutin (C-R, n = 14); diabetes mellitus (DM, n = 16); and DM-rutin (DM-R, n = 16) groups. Seven days after inducing diabetes (streptozotocin, 60 mg/kg, i.p.), rutin was injected intraperitoneally once a week (50 mg/kg) for 7 weeks. Echocardiogram was performed and myocardial function assessed in left ventricular (LV) papillary muscles. Serum insulin concentration was measured by ELISA. One-way ANOVA and Tukey's post hoc test. Glycemia was higher in DM than DM-R and C and in DM-R than C-R. Insulin concentration was lower in diabetic groups than controls (C 2.45 ± 0.67; C-R 2.09 ± 0.52; DM 0.59 ± 0.18; DM-R 0.82 ± 0.21 ng/mL). Echocardiogram showed no differences between C-R and C. DM had increased LV systolic diameter compared to C, and increased left atrium diameter/body weight (BW) ratio and LV mass/BW ratio compared to C and DM-R. Septal wall thickness, LV diastolic diameter/BW ratio, and relative wall thickness were lower in DM-R than DM. Fractional shortening and posterior wall shortening velocity were lower in DM than C and DM-R. In papillary muscle preparation, DM and DM-R presented higher time to peak tension and time from peak tension to 50% relaxation than controls; time to peak tension was lower in DM-R than DM. Under 0.625 and 1.25 mM extracellular calcium concentrations, DM had higher developed tension than C. Rutin attenuates cardiac remodeling and left ventricular and myocardial dysfunction caused by streptozotocin-induced diabetes mellitus.
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spelling Rutin administration attenuates myocardial dysfunction in diabetic ratsOxidative stress plays a major role in diabetic cardiomyopathy pathogenesis. Anti-oxidant therapy has been investigated in preventing or treating several diabetic complications. However, anti-oxidant action on diabetic-induced cardiac remodeling is not completely clear. This study evaluated the effects of rutin, a flavonoid, on cardiac and myocardial function in diabetic rats. Wistar rats were assigned into control (C, n = 14); control-rutin (C-R, n = 14); diabetes mellitus (DM, n = 16); and DM-rutin (DM-R, n = 16) groups. Seven days after inducing diabetes (streptozotocin, 60 mg/kg, i.p.), rutin was injected intraperitoneally once a week (50 mg/kg) for 7 weeks. Echocardiogram was performed and myocardial function assessed in left ventricular (LV) papillary muscles. Serum insulin concentration was measured by ELISA. One-way ANOVA and Tukey's post hoc test. Glycemia was higher in DM than DM-R and C and in DM-R than C-R. Insulin concentration was lower in diabetic groups than controls (C 2.45 ± 0.67; C-R 2.09 ± 0.52; DM 0.59 ± 0.18; DM-R 0.82 ± 0.21 ng/mL). Echocardiogram showed no differences between C-R and C. DM had increased LV systolic diameter compared to C, and increased left atrium diameter/body weight (BW) ratio and LV mass/BW ratio compared to C and DM-R. Septal wall thickness, LV diastolic diameter/BW ratio, and relative wall thickness were lower in DM-R than DM. Fractional shortening and posterior wall shortening velocity were lower in DM than C and DM-R. In papillary muscle preparation, DM and DM-R presented higher time to peak tension and time from peak tension to 50% relaxation than controls; time to peak tension was lower in DM-R than DM. Under 0.625 and 1.25 mM extracellular calcium concentrations, DM had higher developed tension than C. Rutin attenuates cardiac remodeling and left ventricular and myocardial dysfunction caused by streptozotocin-induced diabetes mellitus.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Pró-Reitoria de Pesquisa da UNESP (PROPe)Departamento de Medicina Interna, Faculdade de Medicina de Botucatu (FMB), Universidade Estadual Paulista (UNESP), Botucatu, SP, BrasilDepartamento de Química e Bioquímica, Instituto de Biociências de Botucatu (IBB), Universidade Estadual Paulista (UNESP), Botucatu, SP, BrasilDepartamento de Clínica Médica, Faculdade de Medicina de Botucatu (FMB), Universidade Estadual Paulista (UNESP), Botucatu, SP, BrasilUniversidade Estadual Paulista, Departamento de Clínica Médica, Faculdade de Medicina de BotucatuUniversidade Estadual Paulista, Departamento de Química e Bioquímica, Instituto de Biociências de BotucatuCNPq: 306845/2012-1CNPq: 306857/2012-0)FAPESP: 2009/54506-7BioMed CentralUniversidade Estadual Paulista (Unesp)Guimarães, Julliano F. C. [UNESP]Muzio, Bruno P. [UNESP]Rosa, Camila M. [UNESP]Nascimento, André F. [UNESP]Sugizaki, Mário M. [UNESP]Fernandes, Ana A. H. [UNESP]Cicogna, Antonio C. [UNESP]Padovani, Carlos R. [UNESP]Okoshi, Marina P. [UNESP]Okoshi, Katashi [UNESP]2015-12-07T15:31:32Z2015-12-07T15:31:32Z2015info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article90-96application/pdfhttp://dx.doi.org/10.1186/s12933-015-0255-7Cardiovascular Diabetology, v. 14, p. 90-96, 2015.1475-2840http://hdl.handle.net/11449/13109310.1186/s12933-015-0255-7PMC4504040.pdf159097157630942026185015PMC4504040PubMedreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengCardiovascular Diabetology5.2352,157info:eu-repo/semantics/openAccess2024-08-14T17:23:44Zoai:repositorio.unesp.br:11449/131093Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:23:44Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Rutin administration attenuates myocardial dysfunction in diabetic rats
title Rutin administration attenuates myocardial dysfunction in diabetic rats
spellingShingle Rutin administration attenuates myocardial dysfunction in diabetic rats
Guimarães, Julliano F. C. [UNESP]
title_short Rutin administration attenuates myocardial dysfunction in diabetic rats
title_full Rutin administration attenuates myocardial dysfunction in diabetic rats
title_fullStr Rutin administration attenuates myocardial dysfunction in diabetic rats
title_full_unstemmed Rutin administration attenuates myocardial dysfunction in diabetic rats
title_sort Rutin administration attenuates myocardial dysfunction in diabetic rats
author Guimarães, Julliano F. C. [UNESP]
author_facet Guimarães, Julliano F. C. [UNESP]
Muzio, Bruno P. [UNESP]
Rosa, Camila M. [UNESP]
Nascimento, André F. [UNESP]
Sugizaki, Mário M. [UNESP]
Fernandes, Ana A. H. [UNESP]
Cicogna, Antonio C. [UNESP]
Padovani, Carlos R. [UNESP]
Okoshi, Marina P. [UNESP]
Okoshi, Katashi [UNESP]
author_role author
author2 Muzio, Bruno P. [UNESP]
Rosa, Camila M. [UNESP]
Nascimento, André F. [UNESP]
Sugizaki, Mário M. [UNESP]
Fernandes, Ana A. H. [UNESP]
Cicogna, Antonio C. [UNESP]
Padovani, Carlos R. [UNESP]
Okoshi, Marina P. [UNESP]
Okoshi, Katashi [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Guimarães, Julliano F. C. [UNESP]
Muzio, Bruno P. [UNESP]
Rosa, Camila M. [UNESP]
Nascimento, André F. [UNESP]
Sugizaki, Mário M. [UNESP]
Fernandes, Ana A. H. [UNESP]
Cicogna, Antonio C. [UNESP]
Padovani, Carlos R. [UNESP]
Okoshi, Marina P. [UNESP]
Okoshi, Katashi [UNESP]
description Oxidative stress plays a major role in diabetic cardiomyopathy pathogenesis. Anti-oxidant therapy has been investigated in preventing or treating several diabetic complications. However, anti-oxidant action on diabetic-induced cardiac remodeling is not completely clear. This study evaluated the effects of rutin, a flavonoid, on cardiac and myocardial function in diabetic rats. Wistar rats were assigned into control (C, n = 14); control-rutin (C-R, n = 14); diabetes mellitus (DM, n = 16); and DM-rutin (DM-R, n = 16) groups. Seven days after inducing diabetes (streptozotocin, 60 mg/kg, i.p.), rutin was injected intraperitoneally once a week (50 mg/kg) for 7 weeks. Echocardiogram was performed and myocardial function assessed in left ventricular (LV) papillary muscles. Serum insulin concentration was measured by ELISA. One-way ANOVA and Tukey's post hoc test. Glycemia was higher in DM than DM-R and C and in DM-R than C-R. Insulin concentration was lower in diabetic groups than controls (C 2.45 ± 0.67; C-R 2.09 ± 0.52; DM 0.59 ± 0.18; DM-R 0.82 ± 0.21 ng/mL). Echocardiogram showed no differences between C-R and C. DM had increased LV systolic diameter compared to C, and increased left atrium diameter/body weight (BW) ratio and LV mass/BW ratio compared to C and DM-R. Septal wall thickness, LV diastolic diameter/BW ratio, and relative wall thickness were lower in DM-R than DM. Fractional shortening and posterior wall shortening velocity were lower in DM than C and DM-R. In papillary muscle preparation, DM and DM-R presented higher time to peak tension and time from peak tension to 50% relaxation than controls; time to peak tension was lower in DM-R than DM. Under 0.625 and 1.25 mM extracellular calcium concentrations, DM had higher developed tension than C. Rutin attenuates cardiac remodeling and left ventricular and myocardial dysfunction caused by streptozotocin-induced diabetes mellitus.
publishDate 2015
dc.date.none.fl_str_mv 2015-12-07T15:31:32Z
2015-12-07T15:31:32Z
2015
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/s12933-015-0255-7
Cardiovascular Diabetology, v. 14, p. 90-96, 2015.
1475-2840
http://hdl.handle.net/11449/131093
10.1186/s12933-015-0255-7
PMC4504040.pdf
1590971576309420
26185015
PMC4504040
url http://dx.doi.org/10.1186/s12933-015-0255-7
http://hdl.handle.net/11449/131093
identifier_str_mv Cardiovascular Diabetology, v. 14, p. 90-96, 2015.
1475-2840
10.1186/s12933-015-0255-7
PMC4504040.pdf
1590971576309420
26185015
PMC4504040
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Cardiovascular Diabetology
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dc.format.none.fl_str_mv 90-96
application/pdf
dc.publisher.none.fl_str_mv BioMed Central
publisher.none.fl_str_mv BioMed Central
dc.source.none.fl_str_mv PubMed
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