Aldosterone Blockade Reduces Mortality without Changing Cardiac Remodeling in Spontaneously Hypertensive Rats

Detalhes bibliográficos
Autor(a) principal: Cezar, Marcelo D. M. [UNESP]
Data de Publicação: 2013
Outros Autores: 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]
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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spelling 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/openAccess2024-01-10T06:25:10Zoai:repositorio.unesp.br:11449/112184Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-10T06:25:10Repositório 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
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