Diabetes mellitus activates fetal gene program and intensifies cardiac remodeling and oxidative stress in aged spontaneously hypertensive rats

Detalhes bibliográficos
Autor(a) principal: Rosa, Camila Moreno [UNESP]
Data de Publicação: 2013
Outros Autores: 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]
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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spelling 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
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