Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive 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/10.1159/000430310 http://hdl.handle.net/11449/171927 |
Resumo: | Background: We evaluated the role of the aldosterone blocker spironolactone in attenuating long-term pressure overload-induced cardiac remodeling and heart failure (HF) in spontaneously hypertensive rats (SHR). Methods and Results: Thirteen month-old male SHR were assigned to control (SHR-C, n=20) or spironolactone (SHR-SPR, 20 mg/kg/day, n=24) groups for six months. Normotensive Wistar-Kyoto rats (WKY, n=15) were used as controls. Systolic blood pressure was higher in SHR groups and unchanged by spironolactone. Right ventricular hypertrophy, which characterizes HF in SHR, was less frequent in SHR-SPR than SHR-C. Echocardiographic parameters did not differ between SHR groups. Myocardial function was improved in SHR-SPR compared to SHR-C [developed tension: WKY 4.85±0.68; SHR-C 5.22±1.64; SHR-SPR 6.80±1.49 g/mm2; -dT/dt: WKY 18.0 (16.0-19.0); SHR-C 20.8 (18.4-25.1); SHR-SPR 28.9 (24.2-34.6) g/mm2/s]. Cardiomyocyte cross-sectional area and total collagen concentration (WKY 1.06±0.34; SHR-C 1.85±0.63; SHR-SPR 1.28±0.39 μg/mg wet tissue) were greater in SHR-C than WKY and SHR-SPR. Type 3 collagen expression was lower in SHR-C than WKY and unchanged by spironolactone. Soluble collagen, type I collagen, and lysyl oxidase did not differ between groups. Conclusion: Early spironolactone treatment decreases heart failure development frequency by improving myocardial systolic and diastolic function and attenuating hypertrophy and fibrosis in spontaneously hypertensive rats. |
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Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive RatsAldosterone antagonistCardiac remodelingCollagenPapillary muscleSpontaneously hypertensive ratVentricular functionBackground: We evaluated the role of the aldosterone blocker spironolactone in attenuating long-term pressure overload-induced cardiac remodeling and heart failure (HF) in spontaneously hypertensive rats (SHR). Methods and Results: Thirteen month-old male SHR were assigned to control (SHR-C, n=20) or spironolactone (SHR-SPR, 20 mg/kg/day, n=24) groups for six months. Normotensive Wistar-Kyoto rats (WKY, n=15) were used as controls. Systolic blood pressure was higher in SHR groups and unchanged by spironolactone. Right ventricular hypertrophy, which characterizes HF in SHR, was less frequent in SHR-SPR than SHR-C. Echocardiographic parameters did not differ between SHR groups. Myocardial function was improved in SHR-SPR compared to SHR-C [developed tension: WKY 4.85±0.68; SHR-C 5.22±1.64; SHR-SPR 6.80±1.49 g/mm2; -dT/dt: WKY 18.0 (16.0-19.0); SHR-C 20.8 (18.4-25.1); SHR-SPR 28.9 (24.2-34.6) g/mm2/s]. Cardiomyocyte cross-sectional area and total collagen concentration (WKY 1.06±0.34; SHR-C 1.85±0.63; SHR-SPR 1.28±0.39 μg/mg wet tissue) were greater in SHR-C than WKY and SHR-SPR. Type 3 collagen expression was lower in SHR-C than WKY and unchanged by spironolactone. Soluble collagen, type I collagen, and lysyl oxidase did not differ between groups. Conclusion: Early spironolactone treatment decreases heart failure development frequency by improving myocardial systolic and diastolic function and attenuating hypertrophy and fibrosis in spontaneously hypertensive rats.Department of Internal Medicine Botucatu Medical School Sao Paulo State University UNESP BotucatuFederal University of Mato Grosso Do sulDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP Rubiao JuniorDepartment of Internal Medicine Botucatu Medical School Sao Paulo State University UNESP BotucatuDepartamento de Clinica Medica Faculdade de Medicina de Botucatu UNESP Rubiao JuniorUniversidade Estadual Paulista (Unesp)Federal University of Mato Grosso Do sulCezar, Marcelo D.M. [UNESP]Damatto, Ricardo L. [UNESP]Pagan, Luana U. [UNESP]Lima, Aline R.R. [UNESP]Martinez, Paula F.Bonomo, Camila [UNESP]Rosa, Camila M. [UNESP]Campos, Dijon H.S. [UNESP]Cicogna, Antonio C. [UNESP]Gomes, Mariana J. [UNESP]Oliveira, Silvio A.Blotta, Daniella A. [UNESP]Okoshi, Marina P. [UNESP]Okoshi, Katashi [UNESP]2018-12-11T16:57:46Z2018-12-11T16:57:46Z2015-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1453-1466application/pdfhttp://dx.doi.org/10.1159/000430310Cellular Physiology and Biochemistry, v. 36, n. 4, p. 1453-1466, 2015.1421-97781015-8987http://hdl.handle.net/11449/17192710.1159/0004303102-s2.0-849369715882-s2.0-84936971588.pdf1590971576309420Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengCellular Physiology and Biochemistry1,5611,561info:eu-repo/semantics/openAccess2024-08-14T17:23:43Zoai:repositorio.unesp.br:11449/171927Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:23:43Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats |
title |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats |
spellingShingle |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats Cezar, Marcelo D.M. [UNESP] Aldosterone antagonist Cardiac remodeling Collagen Papillary muscle Spontaneously hypertensive rat Ventricular function |
title_short |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats |
title_full |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats |
title_fullStr |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats |
title_full_unstemmed |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats |
title_sort |
Early Spironolactone Treatment Attenuates Heart Failure Development by Improving Myocardial Function and Reducing Fibrosis in Spontaneously Hypertensive Rats |
author |
Cezar, Marcelo D.M. [UNESP] |
author_facet |
Cezar, Marcelo D.M. [UNESP] Damatto, Ricardo L. [UNESP] Pagan, Luana U. [UNESP] Lima, Aline R.R. [UNESP] Martinez, Paula F. Bonomo, Camila [UNESP] Rosa, Camila M. [UNESP] Campos, Dijon H.S. [UNESP] Cicogna, Antonio C. [UNESP] Gomes, Mariana J. [UNESP] Oliveira, Silvio A. Blotta, Daniella A. [UNESP] Okoshi, Marina P. [UNESP] Okoshi, Katashi [UNESP] |
author_role |
author |
author2 |
Damatto, Ricardo L. [UNESP] Pagan, Luana U. [UNESP] Lima, Aline R.R. [UNESP] Martinez, Paula F. Bonomo, Camila [UNESP] Rosa, Camila M. [UNESP] Campos, Dijon H.S. [UNESP] Cicogna, Antonio C. [UNESP] Gomes, Mariana J. [UNESP] Oliveira, Silvio A. Blotta, Daniella A. [UNESP] Okoshi, Marina P. [UNESP] Okoshi, Katashi [UNESP] |
author2_role |
author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Federal University of Mato Grosso Do sul |
dc.contributor.author.fl_str_mv |
Cezar, Marcelo D.M. [UNESP] Damatto, Ricardo L. [UNESP] Pagan, Luana U. [UNESP] Lima, Aline R.R. [UNESP] Martinez, Paula F. Bonomo, Camila [UNESP] Rosa, Camila M. [UNESP] Campos, Dijon H.S. [UNESP] Cicogna, Antonio C. [UNESP] Gomes, Mariana J. [UNESP] Oliveira, Silvio A. Blotta, Daniella A. [UNESP] Okoshi, Marina P. [UNESP] Okoshi, Katashi [UNESP] |
dc.subject.por.fl_str_mv |
Aldosterone antagonist Cardiac remodeling Collagen Papillary muscle Spontaneously hypertensive rat Ventricular function |
topic |
Aldosterone antagonist Cardiac remodeling Collagen Papillary muscle Spontaneously hypertensive rat Ventricular function |
description |
Background: We evaluated the role of the aldosterone blocker spironolactone in attenuating long-term pressure overload-induced cardiac remodeling and heart failure (HF) in spontaneously hypertensive rats (SHR). Methods and Results: Thirteen month-old male SHR were assigned to control (SHR-C, n=20) or spironolactone (SHR-SPR, 20 mg/kg/day, n=24) groups for six months. Normotensive Wistar-Kyoto rats (WKY, n=15) were used as controls. Systolic blood pressure was higher in SHR groups and unchanged by spironolactone. Right ventricular hypertrophy, which characterizes HF in SHR, was less frequent in SHR-SPR than SHR-C. Echocardiographic parameters did not differ between SHR groups. Myocardial function was improved in SHR-SPR compared to SHR-C [developed tension: WKY 4.85±0.68; SHR-C 5.22±1.64; SHR-SPR 6.80±1.49 g/mm2; -dT/dt: WKY 18.0 (16.0-19.0); SHR-C 20.8 (18.4-25.1); SHR-SPR 28.9 (24.2-34.6) g/mm2/s]. Cardiomyocyte cross-sectional area and total collagen concentration (WKY 1.06±0.34; SHR-C 1.85±0.63; SHR-SPR 1.28±0.39 μg/mg wet tissue) were greater in SHR-C than WKY and SHR-SPR. Type 3 collagen expression was lower in SHR-C than WKY and unchanged by spironolactone. Soluble collagen, type I collagen, and lysyl oxidase did not differ between groups. Conclusion: Early spironolactone treatment decreases heart failure development frequency by improving myocardial systolic and diastolic function and attenuating hypertrophy and fibrosis in spontaneously hypertensive rats. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-01-01 2018-12-11T16:57:46Z 2018-12-11T16:57:46Z |
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/10.1159/000430310 Cellular Physiology and Biochemistry, v. 36, n. 4, p. 1453-1466, 2015. 1421-9778 1015-8987 http://hdl.handle.net/11449/171927 10.1159/000430310 2-s2.0-84936971588 2-s2.0-84936971588.pdf 1590971576309420 |
url |
http://dx.doi.org/10.1159/000430310 http://hdl.handle.net/11449/171927 |
identifier_str_mv |
Cellular Physiology and Biochemistry, v. 36, n. 4, p. 1453-1466, 2015. 1421-9778 1015-8987 10.1159/000430310 2-s2.0-84936971588 2-s2.0-84936971588.pdf 1590971576309420 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Cellular Physiology and Biochemistry 1,561 1,561 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1453-1466 application/pdf |
dc.source.none.fl_str_mv |
Scopus 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_ |
1808128175269478400 |