The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients

Detalhes bibliográficos
Autor(a) principal: Costa, A. R. [UNIFESP]
Data de Publicação: 2009
Outros Autores: Torres, L. B. [UNIFESP], Medei, E., Ricardo, R. A., França, Jerônimo Pereira [UNIFESP], Smaili, Soraya Soubhi [UNIFESP], Nascimento, J. H. M., Oshiro, M. E. M. [UNIFESP], Bassani, J. W. M., Ferreira, Alice Teixeira [UNIFESP], Tucci, Paulo José Ferreira [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1111/j.1476-5381.2009.00329.x
http://repositorio.unifesp.br/handle/11600/31754
Resumo: Background and purpose:Adding spironolactone to standard therapy in heart failure reduces morbidity and mortality, but the underlying mechanisms are not fully understood. We analysed the effect of canrenone, the major active metabolite of spironolactone, on myocardial contractility and intracellular calcium homeostasis.Experimental approach:Left ventricular papillary muscles and cardiomyocytes were isolated from male Wistar rats. Contractility of papillary muscles was assessed with force transducers, Ca(2+) transients by fluorescence and Ca(2+) fluxes by electrophysiological techniques.Key results:Canrenone (300-600 mu mol center dot L(-1)) reduced developed tension, maximum rate of tension increase and maximum rate of tension decay of papillary muscles. in cardiomyocytes, canrenone (50 mu mol center dot L(-1)) reduced cell shortening and L-type Ca(2+) channel current, whereas steady-state activation and inactivation, and reactivation curves were unchanged. Canrenone also decreased the Ca(2+) content of the sarcoplasmic reticulum, intracellular Ca(2+) transient amplitude and intracellular diastolic Ca(2+) concentration. However, the time course of [Ca(2+)](i) decline during transients evoked by caffeine was not affected by canrenone.Conclusion and implications:Canrenone reduced L-type Ca(2+) channel current, amplitude of intracellular Ca(2+) transients and Ca(2+) content of sarcoplasmic reticulum in cardiomyocytes. These changes are likely to underlie the negative inotropic effect of canrenone.
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spelling The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transientsspironolactonecanrenonecalciumcalcium channelsarcoplasmic reticulumBackground and purpose:Adding spironolactone to standard therapy in heart failure reduces morbidity and mortality, but the underlying mechanisms are not fully understood. We analysed the effect of canrenone, the major active metabolite of spironolactone, on myocardial contractility and intracellular calcium homeostasis.Experimental approach:Left ventricular papillary muscles and cardiomyocytes were isolated from male Wistar rats. Contractility of papillary muscles was assessed with force transducers, Ca(2+) transients by fluorescence and Ca(2+) fluxes by electrophysiological techniques.Key results:Canrenone (300-600 mu mol center dot L(-1)) reduced developed tension, maximum rate of tension increase and maximum rate of tension decay of papillary muscles. in cardiomyocytes, canrenone (50 mu mol center dot L(-1)) reduced cell shortening and L-type Ca(2+) channel current, whereas steady-state activation and inactivation, and reactivation curves were unchanged. Canrenone also decreased the Ca(2+) content of the sarcoplasmic reticulum, intracellular Ca(2+) transient amplitude and intracellular diastolic Ca(2+) concentration. However, the time course of [Ca(2+)](i) decline during transients evoked by caffeine was not affected by canrenone.Conclusion and implications:Canrenone reduced L-type Ca(2+) channel current, amplitude of intracellular Ca(2+) transients and Ca(2+) content of sarcoplasmic reticulum in cardiomyocytes. These changes are likely to underlie the negative inotropic effect of canrenone.Universidade Federal de São Paulo, Dept Med, Div Cardiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pharmacol, São Paulo, BrazilUniv Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, BR-21941 Rio de Janeiro, BrazilUniv Estadual Campinas, Dept Biomed Engn, São Paulo, BrazilUniv Estadual Campinas, Ctr Biomed Engn, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biophys, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Med, Div Cardiol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pharmacol, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biophys, São Paulo, BrazilWeb of ScienceFundacao de Amparo Pesquisa do Estado de São PauloConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundacao de Amparo Pesquisa do Estado de São Paulo: 99/04533-4Fundacao de Amparo Pesquisa do Estado de São Paulo: 05/604578Fundacao de Amparo Pesquisa do Estado de São Paulo: 03/14076-7CNPq: 300632/2005-3CNPq: 300.692/80-3Wiley-BlackwellUniversidade Federal de São Paulo (UNIFESP)Universidade Federal do Rio de Janeiro (UFRJ)Universidade Estadual de Campinas (UNICAMP)Costa, A. R. [UNIFESP]Torres, L. B. [UNIFESP]Medei, E.Ricardo, R. A.França, Jerônimo Pereira [UNIFESP]Smaili, Soraya Soubhi [UNIFESP]Nascimento, J. H. M.Oshiro, M. E. M. [UNIFESP]Bassani, J. W. M.Ferreira, Alice Teixeira [UNIFESP]Tucci, Paulo José Ferreira [UNIFESP]2016-01-24T13:58:38Z2016-01-24T13:58:38Z2009-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion580-587http://dx.doi.org/10.1111/j.1476-5381.2009.00329.xBritish Journal of Pharmacology. Malden: Wiley-Blackwell Publishing, Inc, v. 158, n. 2, p. 580-587, 2009.10.1111/j.1476-5381.2009.00329.x0007-1188http://repositorio.unifesp.br/handle/11600/31754WOS:000269676500020engBritish Journal of Pharmacologyinfo:eu-repo/semantics/openAccesshttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-06-02T09:27:23Zoai:repositorio.unifesp.br/:11600/31754Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-06-02T09:27:23Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
title The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
spellingShingle The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
Costa, A. R. [UNIFESP]
spironolactone
canrenone
calcium
calcium channel
sarcoplasmic reticulum
title_short The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
title_full The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
title_fullStr The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
title_full_unstemmed The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
title_sort The negative inotropic action of canrenone is mediated by L-type calcium current blockade and reduced intracellular calcium transients
author Costa, A. R. [UNIFESP]
author_facet Costa, A. R. [UNIFESP]
Torres, L. B. [UNIFESP]
Medei, E.
Ricardo, R. A.
França, Jerônimo Pereira [UNIFESP]
Smaili, Soraya Soubhi [UNIFESP]
Nascimento, J. H. M.
Oshiro, M. E. M. [UNIFESP]
Bassani, J. W. M.
Ferreira, Alice Teixeira [UNIFESP]
Tucci, Paulo José Ferreira [UNIFESP]
author_role author
author2 Torres, L. B. [UNIFESP]
Medei, E.
Ricardo, R. A.
França, Jerônimo Pereira [UNIFESP]
Smaili, Soraya Soubhi [UNIFESP]
Nascimento, J. H. M.
Oshiro, M. E. M. [UNIFESP]
Bassani, J. W. M.
Ferreira, Alice Teixeira [UNIFESP]
Tucci, Paulo José Ferreira [UNIFESP]
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade Federal do Rio de Janeiro (UFRJ)
Universidade Estadual de Campinas (UNICAMP)
dc.contributor.author.fl_str_mv Costa, A. R. [UNIFESP]
Torres, L. B. [UNIFESP]
Medei, E.
Ricardo, R. A.
França, Jerônimo Pereira [UNIFESP]
Smaili, Soraya Soubhi [UNIFESP]
Nascimento, J. H. M.
Oshiro, M. E. M. [UNIFESP]
Bassani, J. W. M.
Ferreira, Alice Teixeira [UNIFESP]
Tucci, Paulo José Ferreira [UNIFESP]
dc.subject.por.fl_str_mv spironolactone
canrenone
calcium
calcium channel
sarcoplasmic reticulum
topic spironolactone
canrenone
calcium
calcium channel
sarcoplasmic reticulum
description Background and purpose:Adding spironolactone to standard therapy in heart failure reduces morbidity and mortality, but the underlying mechanisms are not fully understood. We analysed the effect of canrenone, the major active metabolite of spironolactone, on myocardial contractility and intracellular calcium homeostasis.Experimental approach:Left ventricular papillary muscles and cardiomyocytes were isolated from male Wistar rats. Contractility of papillary muscles was assessed with force transducers, Ca(2+) transients by fluorescence and Ca(2+) fluxes by electrophysiological techniques.Key results:Canrenone (300-600 mu mol center dot L(-1)) reduced developed tension, maximum rate of tension increase and maximum rate of tension decay of papillary muscles. in cardiomyocytes, canrenone (50 mu mol center dot L(-1)) reduced cell shortening and L-type Ca(2+) channel current, whereas steady-state activation and inactivation, and reactivation curves were unchanged. Canrenone also decreased the Ca(2+) content of the sarcoplasmic reticulum, intracellular Ca(2+) transient amplitude and intracellular diastolic Ca(2+) concentration. However, the time course of [Ca(2+)](i) decline during transients evoked by caffeine was not affected by canrenone.Conclusion and implications:Canrenone reduced L-type Ca(2+) channel current, amplitude of intracellular Ca(2+) transients and Ca(2+) content of sarcoplasmic reticulum in cardiomyocytes. These changes are likely to underlie the negative inotropic effect of canrenone.
publishDate 2009
dc.date.none.fl_str_mv 2009-09-01
2016-01-24T13:58:38Z
2016-01-24T13:58:38Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1111/j.1476-5381.2009.00329.x
British Journal of Pharmacology. Malden: Wiley-Blackwell Publishing, Inc, v. 158, n. 2, p. 580-587, 2009.
10.1111/j.1476-5381.2009.00329.x
0007-1188
http://repositorio.unifesp.br/handle/11600/31754
WOS:000269676500020
url http://dx.doi.org/10.1111/j.1476-5381.2009.00329.x
http://repositorio.unifesp.br/handle/11600/31754
identifier_str_mv British Journal of Pharmacology. Malden: Wiley-Blackwell Publishing, Inc, v. 158, n. 2, p. 580-587, 2009.
10.1111/j.1476-5381.2009.00329.x
0007-1188
WOS:000269676500020
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv British Journal of Pharmacology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.format.none.fl_str_mv 580-587
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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