Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in 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/10.1159/000354526 http://hdl.handle.net/11449/112184 |
Resumo: | Background: The role of aldosterone blockers during transition from long-term compensated hypertrophy to dilated failure is not completely understood. In this study we evaluated the effects of early administration of spironolactone on cardiac remodeling, myocardial function, and mortality in spontaneously hypertensive rats (SHR). Methods: Sixteen-month-old SHR received no treatment (SHR-C, n=72) or spironolactone (SHR-SPR, 20 mg/kg/day, n=34) for six months. Echocardiogram was performed before and after treatment. Myocardial function was analyzed in left ventricular (LV) papillary muscle preparations. Myocardial collagen aund hydroxyproline concentration were evaluated by morphometry and spectrophotometry, respectively. LV gene expression was assessed by real time RT-PCR. Statistics: Student's t test; Log rank test (Kaplan Meyer). Results: SHR-C and SHR-SPR presented mortality rates of 71 and 38%, respectively (p=0.004). Systolic arterial pressure did not differ between groups (SHR-C 199 +/- 43; SHR-SPR 200 +/- 35 mmHg). Initial and final echocardiograms did not show significant differences in cardiac structures or LV function between groups. Myocardial function was similar between groups at basal and after inotropic stimulation. Collagen fractional area, hydroxyproline concentration, gene expression for alpha- and beta-myosin heavy chain, atrial natriuretic peptide, and Serca2a were not different between groups. Conclusion: Early spironolactone administration reduces mortality without changing cardiac remodeling in spontaneous hypertensive rats. Copyright (C) 2013 S. Karger AG, Basel |
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Repositório Institucional da UNESP |
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Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive RatsHeart failureMyocardial functionEchocardiogramSpironolactoneVentricular functionPapillary muscleBackground: The role of aldosterone blockers during transition from long-term compensated hypertrophy to dilated failure is not completely understood. In this study we evaluated the effects of early administration of spironolactone on cardiac remodeling, myocardial function, and mortality in spontaneously hypertensive rats (SHR). Methods: Sixteen-month-old SHR received no treatment (SHR-C, n=72) or spironolactone (SHR-SPR, 20 mg/kg/day, n=34) for six months. Echocardiogram was performed before and after treatment. Myocardial function was analyzed in left ventricular (LV) papillary muscle preparations. Myocardial collagen aund hydroxyproline concentration were evaluated by morphometry and spectrophotometry, respectively. LV gene expression was assessed by real time RT-PCR. Statistics: Student's t test; Log rank test (Kaplan Meyer). Results: SHR-C and SHR-SPR presented mortality rates of 71 and 38%, respectively (p=0.004). Systolic arterial pressure did not differ between groups (SHR-C 199 +/- 43; SHR-SPR 200 +/- 35 mmHg). Initial and final echocardiograms did not show significant differences in cardiac structures or LV function between groups. Myocardial function was similar between groups at basal and after inotropic stimulation. Collagen fractional area, hydroxyproline concentration, gene expression for alpha- and beta-myosin heavy chain, atrial natriuretic peptide, and Serca2a were not different between groups. Conclusion: Early spironolactone administration reduces mortality without changing cardiac remodeling in spontaneous hypertensive rats. Copyright (C) 2013 S. Karger AG, BaselConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Sao Paulo State Univ, Botucatu Med Sch, Dept Internal Med, Botucatu, SP, BrazilUNESP, Botucatu Med Sch, BR-18618970 Botucatu, SP, BrazilUniv Fed Mato Grosso do Sul, Campo Grande, BrazilSao Paulo State Univ, Botucatu Med Sch, Dept Internal Med, Botucatu, SP, BrazilUNESP, Botucatu Med Sch, BR-18618970 Botucatu, SP, BrazilCNPq: 305013/2009-0CNPq: 304998/2009-5FAPESP: 07/57497-3FAPESP: 09/54407-9FAPESP: 09/54506-7KargerUniversidade Estadual Paulista (Unesp)Universidade Federal de Mato Grosso do Sul (UFMS)Cezar, Marcelo D. M. [UNESP]Damatto, Ricardo L. [UNESP]Martinez, Paula F.Lima, Aline R. R. [UNESP]Campos, Dijon H. S. [UNESP]Rosa, Camila M. [UNESP]Guizoni, Daniele M. [UNESP]Bonomo, Camila [UNESP]Cicogna, Antonio Carlos [UNESP]Gimenes, Rodrigo [UNESP]Pagan, Luana U. [UNESP]Okoshi, Marina Politi [UNESP]Okoshi, Katashi [UNESP]2014-12-03T13:10:29Z2014-12-03T13:10:29Z2013-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1275-1287application/pdfhttp://dx.doi.org/10.1159/000354526Cellular Physiology And Biochemistry. Basel: Karger, v. 32, n. 5, p. 1275-1287, 2013.1015-8987http://hdl.handle.net/11449/11218410.1159/000354526WOS:000328699600014WOS000328699600014.pdf941897010356413744631386719984321590971576309420Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengCellular Physiology and Biochemistry5.5001,561info:eu-repo/semantics/openAccess2024-08-14T17:36:42Zoai:repositorio.unesp.br:11449/112184Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-14T17:36:42Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats |
title |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats |
spellingShingle |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats Cezar, Marcelo D. M. [UNESP] Heart failure Myocardial function Echocardiogram Spironolactone Ventricular function Papillary muscle |
title_short |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats |
title_full |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats |
title_fullStr |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats |
title_full_unstemmed |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats |
title_sort |
Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats |
author |
Cezar, Marcelo D. M. [UNESP] |
author_facet |
Cezar, Marcelo D. M. [UNESP] Damatto, Ricardo L. [UNESP] Martinez, Paula F. Lima, Aline R. R. [UNESP] Campos, Dijon H. S. [UNESP] Rosa, Camila M. [UNESP] Guizoni, Daniele M. [UNESP] Bonomo, Camila [UNESP] Cicogna, Antonio Carlos [UNESP] Gimenes, Rodrigo [UNESP] Pagan, Luana U. [UNESP] Okoshi, Marina Politi [UNESP] Okoshi, Katashi [UNESP] |
author_role |
author |
author2 |
Damatto, Ricardo L. [UNESP] Martinez, Paula F. Lima, Aline R. R. [UNESP] Campos, Dijon H. S. [UNESP] Rosa, Camila M. [UNESP] Guizoni, Daniele M. [UNESP] Bonomo, Camila [UNESP] Cicogna, Antonio Carlos [UNESP] Gimenes, Rodrigo [UNESP] Pagan, Luana U. [UNESP] Okoshi, Marina Politi [UNESP] Okoshi, Katashi [UNESP] |
author2_role |
author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade Federal de Mato Grosso do Sul (UFMS) |
dc.contributor.author.fl_str_mv |
Cezar, Marcelo D. M. [UNESP] Damatto, Ricardo L. [UNESP] Martinez, Paula F. Lima, Aline R. R. [UNESP] Campos, Dijon H. S. [UNESP] Rosa, Camila M. [UNESP] Guizoni, Daniele M. [UNESP] Bonomo, Camila [UNESP] Cicogna, Antonio Carlos [UNESP] Gimenes, Rodrigo [UNESP] Pagan, Luana U. [UNESP] Okoshi, Marina Politi [UNESP] Okoshi, Katashi [UNESP] |
dc.subject.por.fl_str_mv |
Heart failure Myocardial function Echocardiogram Spironolactone Ventricular function Papillary muscle |
topic |
Heart failure Myocardial function Echocardiogram Spironolactone Ventricular function Papillary muscle |
description |
Background: The role of aldosterone blockers during transition from long-term compensated hypertrophy to dilated failure is not completely understood. In this study we evaluated the effects of early administration of spironolactone on cardiac remodeling, myocardial function, and mortality in spontaneously hypertensive rats (SHR). Methods: Sixteen-month-old SHR received no treatment (SHR-C, n=72) or spironolactone (SHR-SPR, 20 mg/kg/day, n=34) for six months. Echocardiogram was performed before and after treatment. Myocardial function was analyzed in left ventricular (LV) papillary muscle preparations. Myocardial collagen aund hydroxyproline concentration were evaluated by morphometry and spectrophotometry, respectively. LV gene expression was assessed by real time RT-PCR. Statistics: Student's t test; Log rank test (Kaplan Meyer). Results: SHR-C and SHR-SPR presented mortality rates of 71 and 38%, respectively (p=0.004). Systolic arterial pressure did not differ between groups (SHR-C 199 +/- 43; SHR-SPR 200 +/- 35 mmHg). Initial and final echocardiograms did not show significant differences in cardiac structures or LV function between groups. Myocardial function was similar between groups at basal and after inotropic stimulation. Collagen fractional area, hydroxyproline concentration, gene expression for alpha- and beta-myosin heavy chain, atrial natriuretic peptide, and Serca2a were not different between groups. Conclusion: Early spironolactone administration reduces mortality without changing cardiac remodeling in spontaneous hypertensive rats. Copyright (C) 2013 S. Karger AG, Basel |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-01-01 2014-12-03T13:10:29Z 2014-12-03T13:10:29Z |
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/10.1159/000354526 Cellular Physiology And Biochemistry. Basel: Karger, v. 32, n. 5, p. 1275-1287, 2013. 1015-8987 http://hdl.handle.net/11449/112184 10.1159/000354526 WOS:000328699600014 WOS000328699600014.pdf 9418970103564137 4463138671998432 1590971576309420 |
url |
http://dx.doi.org/10.1159/000354526 http://hdl.handle.net/11449/112184 |
identifier_str_mv |
Cellular Physiology And Biochemistry. Basel: Karger, v. 32, n. 5, p. 1275-1287, 2013. 1015-8987 10.1159/000354526 WOS:000328699600014 WOS000328699600014.pdf 9418970103564137 4463138671998432 1590971576309420 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Cellular Physiology and Biochemistry 5.500 1,561 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1275-1287 application/pdf |
dc.publisher.none.fl_str_mv |
Karger |
publisher.none.fl_str_mv |
Karger |
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_ |
1808128199022870528 |