Rutin administration attenuates myocardial dysfunction in diabetic rats
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , , , |
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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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 5.235 2,157 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128178961514496 |