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Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat

Carvedilol has beneficial effects on cardiac function in patients with heart failure but its effect on ovariectomy-induced myocardial contractile dysfunction remains unclear. Estrogen deficiency induces myocardial contractile dysfunction and increases cardiovascular disease risk in postmenopausal wo...

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Autores principales: Ribeiro, Rogerio Faustino, Potratz, Felipe F., Pavan, Brunella M. M., Forechi, Ludimila, Lima, Filipe Lugon Moulin, Fiorim, Jonaina, Fernandes, Aurelia Araujo, Vassallo, Dalton Valentim, Stefanon, Ivanita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538779/
https://www.ncbi.nlm.nih.gov/pubmed/23308166
http://dx.doi.org/10.1371/journal.pone.0053226
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author Ribeiro, Rogerio Faustino
Potratz, Felipe F.
Pavan, Brunella M. M.
Forechi, Ludimila
Lima, Filipe Lugon Moulin
Fiorim, Jonaina
Fernandes, Aurelia Araujo
Vassallo, Dalton Valentim
Stefanon, Ivanita
author_facet Ribeiro, Rogerio Faustino
Potratz, Felipe F.
Pavan, Brunella M. M.
Forechi, Ludimila
Lima, Filipe Lugon Moulin
Fiorim, Jonaina
Fernandes, Aurelia Araujo
Vassallo, Dalton Valentim
Stefanon, Ivanita
author_sort Ribeiro, Rogerio Faustino
collection PubMed
description Carvedilol has beneficial effects on cardiac function in patients with heart failure but its effect on ovariectomy-induced myocardial contractile dysfunction remains unclear. Estrogen deficiency induces myocardial contractile dysfunction and increases cardiovascular disease risk in postmenopausal women. Our aim was to investigate whether carvedilol, a beta receptor blocker, would prevent ovariectomy-induced myocardial contractile dysfunction. Female rats (8 weeks old) that underwent bilateral ovariectomy were randomly assigned to receive daily treatment with carvedilol (OVX+CAR, 20 mg/kg), placebo (OVX) and SHAM for 58 days. Left ventricle papillary muscle was mounted for isometric tension recordings. The inotropic response to Ca(2+) (0.62 to 3.75 mM) and isoproterenol (Iso 10(−8) to 10(−2 )M) were assessed. Expression of calcium handling proteins was measured by western blot analysis. Carvedilol treatment in the OVX animals: prevented weight gain and slight hypertrophy, restored the reduced positive inotropic responses to Ca(2+) and isoproterenol, prevented the reduction in SERCA2a expression, abolished the increase in superoxide anion production, normalized the increase in p22(phox) expression, and decreased serum angiotensin converting enzyme (ACE) activity. This study demonstrated that myocardial contractile dysfunction and SERCA2a down regulation were prevented by carvedilol treatment. Superoxide anion production and NADPH oxidase seem to be involved in this response.
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spelling pubmed-35387792013-01-10 Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat Ribeiro, Rogerio Faustino Potratz, Felipe F. Pavan, Brunella M. M. Forechi, Ludimila Lima, Filipe Lugon Moulin Fiorim, Jonaina Fernandes, Aurelia Araujo Vassallo, Dalton Valentim Stefanon, Ivanita PLoS One Research Article Carvedilol has beneficial effects on cardiac function in patients with heart failure but its effect on ovariectomy-induced myocardial contractile dysfunction remains unclear. Estrogen deficiency induces myocardial contractile dysfunction and increases cardiovascular disease risk in postmenopausal women. Our aim was to investigate whether carvedilol, a beta receptor blocker, would prevent ovariectomy-induced myocardial contractile dysfunction. Female rats (8 weeks old) that underwent bilateral ovariectomy were randomly assigned to receive daily treatment with carvedilol (OVX+CAR, 20 mg/kg), placebo (OVX) and SHAM for 58 days. Left ventricle papillary muscle was mounted for isometric tension recordings. The inotropic response to Ca(2+) (0.62 to 3.75 mM) and isoproterenol (Iso 10(−8) to 10(−2 )M) were assessed. Expression of calcium handling proteins was measured by western blot analysis. Carvedilol treatment in the OVX animals: prevented weight gain and slight hypertrophy, restored the reduced positive inotropic responses to Ca(2+) and isoproterenol, prevented the reduction in SERCA2a expression, abolished the increase in superoxide anion production, normalized the increase in p22(phox) expression, and decreased serum angiotensin converting enzyme (ACE) activity. This study demonstrated that myocardial contractile dysfunction and SERCA2a down regulation were prevented by carvedilol treatment. Superoxide anion production and NADPH oxidase seem to be involved in this response. Public Library of Science 2013-01-07 /pmc/articles/PMC3538779/ /pubmed/23308166 http://dx.doi.org/10.1371/journal.pone.0053226 Text en © 2013 Ribeiro Junior et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ribeiro, Rogerio Faustino
Potratz, Felipe F.
Pavan, Brunella M. M.
Forechi, Ludimila
Lima, Filipe Lugon Moulin
Fiorim, Jonaina
Fernandes, Aurelia Araujo
Vassallo, Dalton Valentim
Stefanon, Ivanita
Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat
title Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat
title_full Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat
title_fullStr Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat
title_full_unstemmed Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat
title_short Carvedilol Prevents Ovariectomy-Induced Myocardial Contractile Dysfunction in Female Rat
title_sort carvedilol prevents ovariectomy-induced myocardial contractile dysfunction in female rat
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538779/
https://www.ncbi.nlm.nih.gov/pubmed/23308166
http://dx.doi.org/10.1371/journal.pone.0053226
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