Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1186/1475-2840-12-152 http://hdl.handle.net/11449/112201 |
Resumo: | Background: The combination of systemic arterial hypertension and diabetes mellitus (DM) induces greater cardiac remodeling than either condition alone. However, this association has been poorly addressed in senescent rats. Therefore, this study aimed to analyze the influence of streptozotocin-induced DM on ventricular remodeling and oxidative stress in aged spontaneously hypertensive rats (SHR).Methods: Fifty 18 month old male SHR were divided into two groups: control (SHR, n = 25) and diabetic (SHR-DM, n = 25). DM was induced by streptozotocin (40 mg/kg, i.p.). After nine weeks, the rats underwent echocardiography and myocardial functional study in left ventricular (LV) isolated papillary muscle preparations. LV samples were obtained to measure myocyte diameters, interstitial collagen fraction, and hydroxyproline concentration. Gene expression of atrial natriuretic peptide (ANP) and alpha- and beta-myosin heavy chain (MyHC) isoforms was evaluated by RT-PCR. Serum oxidative stress was assessed by measuring lipid hydroperoxide concentration and superoxide dismutase and glutathione peroxidase activities. Statistics: Student's t test or Mann-Whitney test, p < 0.05.Results: SHR-DM presented higher blood glucose (487 +/- 29 vs. 89.1 +/- 21.1 mg/dL) and lower body weight (277 +/- 26 vs. 339 +/- 38 g). Systolic blood pressure did not differ between groups. Echocardiography showed LV and left atrial dilation, LV diastolic and relative wall thickness decrease, and LV systolic and diastolic function impairment in SHR-DM. Papillary muscle study showed decreased myocardial contractility and contractile reserve in SHR-DM. Myocyte diameters and myocardial interstitial collagen fraction and hydroxyproline concentration did not differ between groups. Increased serum pro-oxidant activity and gene expression of ANP and beta/alpha-MyHC ratio were observed in DM.Conclusion: Diabetes mellitus induces cardiac dilation and functional impairment, increases oxidative stress and activates fetal gene program in aged spontaneously hypertensive rats. |
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Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive ratsDiabetes mellitusOxidative stressSystemic hypertensionSpontaneously hypertensive ratsElderlyBackground: The combination of systemic arterial hypertension and diabetes mellitus (DM) induces greater cardiac remodeling than either condition alone. However, this association has been poorly addressed in senescent rats. Therefore, this study aimed to analyze the influence of streptozotocin-induced DM on ventricular remodeling and oxidative stress in aged spontaneously hypertensive rats (SHR).Methods: Fifty 18 month old male SHR were divided into two groups: control (SHR, n = 25) and diabetic (SHR-DM, n = 25). DM was induced by streptozotocin (40 mg/kg, i.p.). After nine weeks, the rats underwent echocardiography and myocardial functional study in left ventricular (LV) isolated papillary muscle preparations. LV samples were obtained to measure myocyte diameters, interstitial collagen fraction, and hydroxyproline concentration. Gene expression of atrial natriuretic peptide (ANP) and alpha- and beta-myosin heavy chain (MyHC) isoforms was evaluated by RT-PCR. Serum oxidative stress was assessed by measuring lipid hydroperoxide concentration and superoxide dismutase and glutathione peroxidase activities. Statistics: Student's t test or Mann-Whitney test, p < 0.05.Results: SHR-DM presented higher blood glucose (487 +/- 29 vs. 89.1 +/- 21.1 mg/dL) and lower body weight (277 +/- 26 vs. 339 +/- 38 g). Systolic blood pressure did not differ between groups. Echocardiography showed LV and left atrial dilation, LV diastolic and relative wall thickness decrease, and LV systolic and diastolic function impairment in SHR-DM. Papillary muscle study showed decreased myocardial contractility and contractile reserve in SHR-DM. Myocyte diameters and myocardial interstitial collagen fraction and hydroxyproline concentration did not differ between groups. Increased serum pro-oxidant activity and gene expression of ANP and beta/alpha-MyHC ratio were observed in DM.Conclusion: Diabetes mellitus induces cardiac dilation and functional impairment, increases oxidative stress and activates fetal gene program in aged spontaneously hypertensive rats.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)Sao Paulo State Univ, UNESP, Botucatu Med Sch, Dept Internal Med, Botucatu, SP, BrazilSao Paulo State Univ, UNESP, Inst Biosci, Dept Chem & Biochem, Botucatu, SP, BrazilUNESP, Fac Med Botucatu, Dept Clin Med, BR-18618970 Botucatu, SP, BrazilSao Paulo State Univ, UNESP, Botucatu Med Sch, Dept Internal Med, Botucatu, SP, BrazilSao Paulo State Univ, UNESP, Inst Biosci, Dept Chem & Biochem, Botucatu, SP, BrazilUNESP, Fac Med Botucatu, Dept Clin Med, BR-18618970 Botucatu, SP, BrazilCNPq: 306845/2012-1CNPq: 306857/2012-0FAPESP: 09/54506-7Biomed Central Ltd.Universidade Estadual Paulista (Unesp)Rosa, Camila Moreno [UNESP]Xavier, Natasha Priscilla [UNESP]Campos, Dijon Henrique [UNESP]Fernandes, Ana Angelica Henrique [UNESP]Mariano Cezar, Marcelo Diarcadia [UNESP]Martinez, Paula Felippe [UNESP]Cicogna, Antonio Carlos [UNESP]Gimenes, Camila [UNESP]Gimenes, Rodrigo [UNESP]Okoshi, Marina Politi [UNESP]Okoshi, Katashi [UNESP]2014-12-03T13:10:30Z2014-12-03T13:10:30Z2013-10-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article9application/pdfhttp://dx.doi.org/10.1186/1475-2840-12-152Cardiovascular Diabetology. London: Biomed Central Ltd, v. 12, 9 p., 2013.1475-2840http://hdl.handle.net/11449/11220110.1186/1475-2840-12-152WOS:000327610800004WOS000327610800004.pdf941897010356413744631386719984321590971576309420Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengCardiovascular Diabetology5.2352,157info:eu-repo/semantics/openAccess2024-08-14T17:22:58Zoai:repositorio.unesp.br:11449/112201Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:22:58Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats |
title |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats |
spellingShingle |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats Rosa, Camila Moreno [UNESP] Diabetes mellitus Oxidative stress Systemic hypertension Spontaneously hypertensive rats Elderly |
title_short |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats |
title_full |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats |
title_fullStr |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats |
title_full_unstemmed |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats |
title_sort |
Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats |
author |
Rosa, Camila Moreno [UNESP] |
author_facet |
Rosa, Camila Moreno [UNESP] Xavier, Natasha Priscilla [UNESP] Campos, Dijon Henrique [UNESP] Fernandes, Ana Angelica Henrique [UNESP] Mariano Cezar, Marcelo Diarcadia [UNESP] Martinez, Paula Felippe [UNESP] Cicogna, Antonio Carlos [UNESP] Gimenes, Camila [UNESP] Gimenes, Rodrigo [UNESP] Okoshi, Marina Politi [UNESP] Okoshi, Katashi [UNESP] |
author_role |
author |
author2 |
Xavier, Natasha Priscilla [UNESP] Campos, Dijon Henrique [UNESP] Fernandes, Ana Angelica Henrique [UNESP] Mariano Cezar, Marcelo Diarcadia [UNESP] Martinez, Paula Felippe [UNESP] Cicogna, Antonio Carlos [UNESP] Gimenes, Camila [UNESP] Gimenes, Rodrigo [UNESP] Okoshi, Marina Politi [UNESP] Okoshi, Katashi [UNESP] |
author2_role |
author 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 |
Rosa, Camila Moreno [UNESP] Xavier, Natasha Priscilla [UNESP] Campos, Dijon Henrique [UNESP] Fernandes, Ana Angelica Henrique [UNESP] Mariano Cezar, Marcelo Diarcadia [UNESP] Martinez, Paula Felippe [UNESP] Cicogna, Antonio Carlos [UNESP] Gimenes, Camila [UNESP] Gimenes, Rodrigo [UNESP] Okoshi, Marina Politi [UNESP] Okoshi, Katashi [UNESP] |
dc.subject.por.fl_str_mv |
Diabetes mellitus Oxidative stress Systemic hypertension Spontaneously hypertensive rats Elderly |
topic |
Diabetes mellitus Oxidative stress Systemic hypertension Spontaneously hypertensive rats Elderly |
description |
Background: The combination of systemic arterial hypertension and diabetes mellitus (DM) induces greater cardiac remodeling than either condition alone. However, this association has been poorly addressed in senescent rats. Therefore, this study aimed to analyze the influence of streptozotocin-induced DM on ventricular remodeling and oxidative stress in aged spontaneously hypertensive rats (SHR).Methods: Fifty 18 month old male SHR were divided into two groups: control (SHR, n = 25) and diabetic (SHR-DM, n = 25). DM was induced by streptozotocin (40 mg/kg, i.p.). After nine weeks, the rats underwent echocardiography and myocardial functional study in left ventricular (LV) isolated papillary muscle preparations. LV samples were obtained to measure myocyte diameters, interstitial collagen fraction, and hydroxyproline concentration. Gene expression of atrial natriuretic peptide (ANP) and alpha- and beta-myosin heavy chain (MyHC) isoforms was evaluated by RT-PCR. Serum oxidative stress was assessed by measuring lipid hydroperoxide concentration and superoxide dismutase and glutathione peroxidase activities. Statistics: Student's t test or Mann-Whitney test, p < 0.05.Results: SHR-DM presented higher blood glucose (487 +/- 29 vs. 89.1 +/- 21.1 mg/dL) and lower body weight (277 +/- 26 vs. 339 +/- 38 g). Systolic blood pressure did not differ between groups. Echocardiography showed LV and left atrial dilation, LV diastolic and relative wall thickness decrease, and LV systolic and diastolic function impairment in SHR-DM. Papillary muscle study showed decreased myocardial contractility and contractile reserve in SHR-DM. Myocyte diameters and myocardial interstitial collagen fraction and hydroxyproline concentration did not differ between groups. Increased serum pro-oxidant activity and gene expression of ANP and beta/alpha-MyHC ratio were observed in DM.Conclusion: Diabetes mellitus induces cardiac dilation and functional impairment, increases oxidative stress and activates fetal gene program in aged spontaneously hypertensive rats. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-10-17 2014-12-03T13:10:30Z 2014-12-03T13:10:30Z |
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/10.1186/1475-2840-12-152 Cardiovascular Diabetology. London: Biomed Central Ltd, v. 12, 9 p., 2013. 1475-2840 http://hdl.handle.net/11449/112201 10.1186/1475-2840-12-152 WOS:000327610800004 WOS000327610800004.pdf 9418970103564137 4463138671998432 1590971576309420 |
url |
http://dx.doi.org/10.1186/1475-2840-12-152 http://hdl.handle.net/11449/112201 |
identifier_str_mv |
Cardiovascular Diabetology. London: Biomed Central Ltd, v. 12, 9 p., 2013. 1475-2840 10.1186/1475-2840-12-152 WOS:000327610800004 WOS000327610800004.pdf 9418970103564137 4463138671998432 1590971576309420 |
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 |
9 application/pdf |
dc.publisher.none.fl_str_mv |
Biomed Central Ltd. |
publisher.none.fl_str_mv |
Biomed Central Ltd. |
dc.source.none.fl_str_mv |
Web of Science 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_ |
1808128140464095232 |