Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion.
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFOP |
Texto Completo: | http://www.repositorio.ufop.br/jspui/handle/123456789/15736 http://dx.doi.org/10.33448/rsd-v11i3.26498 |
Resumo: | Introduction: Mineralocorticoid receptor antagonists (MRAs) are effective in reducing left ventricle remodeling and sudden death after acute myocardial infarction (AMI). Objectives: MRAs in vitro display cardioprotective effects, independent of MR; however, it is unknown whether the rapid effects of MRAs are cardioprotective in vivo. This study evaluated the acute effects of spironolactone and eplerenone in the first minutes of AMI. Methods: Wistar Rats, submitted or not to bilateral adrenalectomy, were treated orally with spironolactone (20 mg/kg) or eplerenone (10 mg/kg), and submitted to the left coronary ligation, under anesthesia. Electrocardiogram (ECG) recordings were obtained to evaluate ST-T segment, QT, and QTc intervals. Arterial pressure was also measured before (baseline) and after coronary ligation. Results: Spironolactone or eplerenone given, one hour before coronary ligation, prevented ST- T segment elevation in adrenalectomized and non-adrenalectomized. QT interval analysis showed that MRAs prevented its prolongation after coronary ligation. QT and QTc intervals remained similar to baseline and were smaller than the values displayed by the non-treated group. Animals treated with spironolactone, regardless of adrenalectomy, showed a 3-fold reduced mortality rates compared to the control group. Conclusion: MRAs display acute cardioprotective effects in early phase of AMI, which are independent of aldosterone. |
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Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion.Espironolactona e eplerenona são cardioprotetoras durante a fase precoce de isquemia em ratos submetidos à oclusão coronária.Acute myocardial infarctionElectrocardiogramInfarto agudo do miocárdioEletrocardiogramaIntroduction: Mineralocorticoid receptor antagonists (MRAs) are effective in reducing left ventricle remodeling and sudden death after acute myocardial infarction (AMI). Objectives: MRAs in vitro display cardioprotective effects, independent of MR; however, it is unknown whether the rapid effects of MRAs are cardioprotective in vivo. This study evaluated the acute effects of spironolactone and eplerenone in the first minutes of AMI. Methods: Wistar Rats, submitted or not to bilateral adrenalectomy, were treated orally with spironolactone (20 mg/kg) or eplerenone (10 mg/kg), and submitted to the left coronary ligation, under anesthesia. Electrocardiogram (ECG) recordings were obtained to evaluate ST-T segment, QT, and QTc intervals. Arterial pressure was also measured before (baseline) and after coronary ligation. Results: Spironolactone or eplerenone given, one hour before coronary ligation, prevented ST- T segment elevation in adrenalectomized and non-adrenalectomized. QT interval analysis showed that MRAs prevented its prolongation after coronary ligation. QT and QTc intervals remained similar to baseline and were smaller than the values displayed by the non-treated group. Animals treated with spironolactone, regardless of adrenalectomy, showed a 3-fold reduced mortality rates compared to the control group. Conclusion: MRAs display acute cardioprotective effects in early phase of AMI, which are independent of aldosterone.Introdução: Os antagonistas do receptor de mineralocorticóide (MRAs) são eficazes na redução da remodelação do ventrículo esquerdo e morte súbita após infarto agudo do miocárdio (IAM). Objetivo: MRAs in vitro apresentam efeitos cardioprotetores, independente do MR; no entanto, não se sabe se os efeitos rápidos dos MRAs são cardioprotetores in vivo. Este estudo avaliou os efeitos agudos da espironolactona e da eplerenona nos primeiros minutos do IAM. Métodos: Ratos Wistar, submetidos ou não à adrenalectomia bilateral, foram tratados por via oral com espironolactona (20 mg / kg) ou eplerenona (10 mg / kg), e submetidos à ligadura da coronária esquerda, sob anestesia. Registros de eletrocardiograma (ECG) foram obtidos para avaliar o segmento ST-T, o intervalo QT e os intervalos QTc. A pressão arterial também foi medida antes (linha de base) e após a ligadura coronária. Resultados: Espironolactona ou eplerenona administrada uma hora antes da ligadura coronária preveniu a elevação do segmento ST-T em adrenalectomizados e não adrenalectomizados. A análise do intervalo QT mostrou que os MRAs impediram seu prolongamento após a ligadura coronária. Os intervalos QT e QTc permaneceram semelhantes à linha de base e foram menores do que os valores exibidos pelo grupo não tratado. Os animais tratados com espironolactona, independentemente da adrenalectomia, apresentaram taxas de mortalidade 3 vezes menores em comparação com o grupo controle. Conclusão: Os MRAs apresentam efeitos cardioprotetores agudos na fase inicial do IAM, que são independentes da aldosterona.2022-11-04T17:03:45Z2022-11-04T17:03:45Z2022info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfAMANCIO, G. de C. S. et al. Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. Research, Society and Development, v. 11, n. 3, 2022. Disponível em: <https://rsdjournal.org/index.php/rsd/article/view/26498>. Acesso em: 11 out. 2022.2525-3409http://www.repositorio.ufop.br/jspui/handle/123456789/15736http://dx.doi.org/10.33448/rsd-v11i3.26498This is an open-access article distributed under the terms of the Creative Commons Attribution License. Fonte: o PDF do artigo.info:eu-repo/semantics/openAccessAmancio, Gabriela de Cássia SousaHermidorff, Milla MarquesAlvarenga, Ana CláudiaLima, Wanderson Geraldo deGuimarães, Homero NogueiraRodrigues, Henrique ResendeSilva, Emília CalilAssis, Leonardo Vinícius Monteiro deGuimarães, Andrea GrabeIsoldi, Mauro Césarengreponame:Repositório Institucional da UFOPinstname:Universidade Federal de Ouro Preto (UFOP)instacron:UFOP2022-11-04T17:03:52Zoai:repositorio.ufop.br:123456789/15736Repositório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332022-11-04T17:03:52Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)false |
dc.title.none.fl_str_mv |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. Espironolactona e eplerenona são cardioprotetoras durante a fase precoce de isquemia em ratos submetidos à oclusão coronária. |
title |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. |
spellingShingle |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. Amancio, Gabriela de Cássia Sousa Acute myocardial infarction Electrocardiogram Infarto agudo do miocárdio Eletrocardiograma |
title_short |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. |
title_full |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. |
title_fullStr |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. |
title_full_unstemmed |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. |
title_sort |
Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. |
author |
Amancio, Gabriela de Cássia Sousa |
author_facet |
Amancio, Gabriela de Cássia Sousa Hermidorff, Milla Marques Alvarenga, Ana Cláudia Lima, Wanderson Geraldo de Guimarães, Homero Nogueira Rodrigues, Henrique Resende Silva, Emília Calil Assis, Leonardo Vinícius Monteiro de Guimarães, Andrea Grabe Isoldi, Mauro César |
author_role |
author |
author2 |
Hermidorff, Milla Marques Alvarenga, Ana Cláudia Lima, Wanderson Geraldo de Guimarães, Homero Nogueira Rodrigues, Henrique Resende Silva, Emília Calil Assis, Leonardo Vinícius Monteiro de Guimarães, Andrea Grabe Isoldi, Mauro César |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Amancio, Gabriela de Cássia Sousa Hermidorff, Milla Marques Alvarenga, Ana Cláudia Lima, Wanderson Geraldo de Guimarães, Homero Nogueira Rodrigues, Henrique Resende Silva, Emília Calil Assis, Leonardo Vinícius Monteiro de Guimarães, Andrea Grabe Isoldi, Mauro César |
dc.subject.por.fl_str_mv |
Acute myocardial infarction Electrocardiogram Infarto agudo do miocárdio Eletrocardiograma |
topic |
Acute myocardial infarction Electrocardiogram Infarto agudo do miocárdio Eletrocardiograma |
description |
Introduction: Mineralocorticoid receptor antagonists (MRAs) are effective in reducing left ventricle remodeling and sudden death after acute myocardial infarction (AMI). Objectives: MRAs in vitro display cardioprotective effects, independent of MR; however, it is unknown whether the rapid effects of MRAs are cardioprotective in vivo. This study evaluated the acute effects of spironolactone and eplerenone in the first minutes of AMI. Methods: Wistar Rats, submitted or not to bilateral adrenalectomy, were treated orally with spironolactone (20 mg/kg) or eplerenone (10 mg/kg), and submitted to the left coronary ligation, under anesthesia. Electrocardiogram (ECG) recordings were obtained to evaluate ST-T segment, QT, and QTc intervals. Arterial pressure was also measured before (baseline) and after coronary ligation. Results: Spironolactone or eplerenone given, one hour before coronary ligation, prevented ST- T segment elevation in adrenalectomized and non-adrenalectomized. QT interval analysis showed that MRAs prevented its prolongation after coronary ligation. QT and QTc intervals remained similar to baseline and were smaller than the values displayed by the non-treated group. Animals treated with spironolactone, regardless of adrenalectomy, showed a 3-fold reduced mortality rates compared to the control group. Conclusion: MRAs display acute cardioprotective effects in early phase of AMI, which are independent of aldosterone. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-11-04T17:03:45Z 2022-11-04T17:03:45Z 2022 |
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 |
AMANCIO, G. de C. S. et al. Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. Research, Society and Development, v. 11, n. 3, 2022. Disponível em: <https://rsdjournal.org/index.php/rsd/article/view/26498>. Acesso em: 11 out. 2022. 2525-3409 http://www.repositorio.ufop.br/jspui/handle/123456789/15736 http://dx.doi.org/10.33448/rsd-v11i3.26498 |
identifier_str_mv |
AMANCIO, G. de C. S. et al. Spironolactone and eplerenone are cardioprotective during early phase of ischemia in rats submitted to acute coronary occlusion. Research, Society and Development, v. 11, n. 3, 2022. Disponível em: <https://rsdjournal.org/index.php/rsd/article/view/26498>. Acesso em: 11 out. 2022. 2525-3409 |
url |
http://www.repositorio.ufop.br/jspui/handle/123456789/15736 http://dx.doi.org/10.33448/rsd-v11i3.26498 |
dc.language.iso.fl_str_mv |
eng |
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eng |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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reponame:Repositório Institucional da UFOP instname:Universidade Federal de Ouro Preto (UFOP) instacron:UFOP |
instname_str |
Universidade Federal de Ouro Preto (UFOP) |
instacron_str |
UFOP |
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UFOP |
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Repositório Institucional da UFOP |
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Repositório Institucional da UFOP |
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Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP) |
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repositorio@ufop.edu.br |
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