Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries

Detalhes bibliográficos
Autor(a) principal: Andrade,Daniela Medeiros Lobo de
Data de Publicação: 2016
Outros Autores: Borges,Leonardo Luis, Torres,Ieda Maria Sapateiro, Conceição,Edemilson Cardoso da, Rocha,Matheus Lavorenti
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Arquivos Brasileiros de Cardiologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2016004200223
Resumo: Abstract Background: Despite the important biological effects of jabuticaba, its actions on the cardiovascular system have not been clarified. Objectives: To determine the effects of jabuticaba hydroalcoholic extract (JHE) on vascular smooth muscle (VSM) of isolated arteries. Methods: Endothelium-denuded aortic rings of rats were mounted in isolated organ bath to record isometric tension. The relaxant effect of JHE and the influence of K+ channels and Ca2+ intra- and extracellular sources on JHE-stimulated response were assessed. Results: Arteries pre-contracted with phenylephrine showed concentration-dependent relaxation (0.380 to 1.92 mg/mL). Treatment with K+ channel blockers (tetraethyl-ammonium, glibenclamide, 4-aminopyridine) hindered relaxation due to JHE. In addition, phenylephrine-stimulated contraction was hindered by previous treatment with JHE. Inhibition of sarcoplasmic reticulum Ca2+ ATPase did not change relaxation due to JHE. In addition, JHE inhibited the contraction caused by Ca2+ influx stimulated by phenylephrine and KCl (75 mM). Conclusion: JHE induces endothelium-independent vasodilation. Activation of K+ channels and inhibition of Ca2+ influx through the membrane are involved in the JHE relaxant effect.
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spelling Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated ArteriesJabuticaba (Myrciaria Cauliflora)TreesVasodilatationCalcium ChannelsMuscle, Smooth VascularAbstract Background: Despite the important biological effects of jabuticaba, its actions on the cardiovascular system have not been clarified. Objectives: To determine the effects of jabuticaba hydroalcoholic extract (JHE) on vascular smooth muscle (VSM) of isolated arteries. Methods: Endothelium-denuded aortic rings of rats were mounted in isolated organ bath to record isometric tension. The relaxant effect of JHE and the influence of K+ channels and Ca2+ intra- and extracellular sources on JHE-stimulated response were assessed. Results: Arteries pre-contracted with phenylephrine showed concentration-dependent relaxation (0.380 to 1.92 mg/mL). Treatment with K+ channel blockers (tetraethyl-ammonium, glibenclamide, 4-aminopyridine) hindered relaxation due to JHE. In addition, phenylephrine-stimulated contraction was hindered by previous treatment with JHE. Inhibition of sarcoplasmic reticulum Ca2+ ATPase did not change relaxation due to JHE. In addition, JHE inhibited the contraction caused by Ca2+ influx stimulated by phenylephrine and KCl (75 mM). Conclusion: JHE induces endothelium-independent vasodilation. Activation of K+ channels and inhibition of Ca2+ influx through the membrane are involved in the JHE relaxant effect.Sociedade Brasileira de Cardiologia - SBC2016-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2016004200223Arquivos Brasileiros de Cardiologia v.107 n.3 2016reponame:Arquivos Brasileiros de Cardiologia (Online)instname:Sociedade Brasileira de Cardiologia (SBC)instacron:SBC10.5935/abc.20160118info:eu-repo/semantics/openAccessAndrade,Daniela Medeiros Lobo deBorges,Leonardo LuisTorres,Ieda Maria SapateiroConceição,Edemilson Cardoso daRocha,Matheus Lavorentieng2016-10-05T00:00:00Zoai:scielo:S0066-782X2016004200223Revistahttp://www.arquivosonline.com.br/https://old.scielo.br/oai/scielo-oai.php||arquivos@cardiol.br1678-41700066-782Xopendoar:2016-10-05T00:00Arquivos Brasileiros de Cardiologia (Online) - Sociedade Brasileira de Cardiologia (SBC)false
dc.title.none.fl_str_mv Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
title Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
spellingShingle Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
Andrade,Daniela Medeiros Lobo de
Jabuticaba (Myrciaria Cauliflora)
Trees
Vasodilatation
Calcium Channels
Muscle, Smooth Vascular
title_short Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
title_full Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
title_fullStr Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
title_full_unstemmed Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
title_sort Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
author Andrade,Daniela Medeiros Lobo de
author_facet Andrade,Daniela Medeiros Lobo de
Borges,Leonardo Luis
Torres,Ieda Maria Sapateiro
Conceição,Edemilson Cardoso da
Rocha,Matheus Lavorenti
author_role author
author2 Borges,Leonardo Luis
Torres,Ieda Maria Sapateiro
Conceição,Edemilson Cardoso da
Rocha,Matheus Lavorenti
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Andrade,Daniela Medeiros Lobo de
Borges,Leonardo Luis
Torres,Ieda Maria Sapateiro
Conceição,Edemilson Cardoso da
Rocha,Matheus Lavorenti
dc.subject.por.fl_str_mv Jabuticaba (Myrciaria Cauliflora)
Trees
Vasodilatation
Calcium Channels
Muscle, Smooth Vascular
topic Jabuticaba (Myrciaria Cauliflora)
Trees
Vasodilatation
Calcium Channels
Muscle, Smooth Vascular
description Abstract Background: Despite the important biological effects of jabuticaba, its actions on the cardiovascular system have not been clarified. Objectives: To determine the effects of jabuticaba hydroalcoholic extract (JHE) on vascular smooth muscle (VSM) of isolated arteries. Methods: Endothelium-denuded aortic rings of rats were mounted in isolated organ bath to record isometric tension. The relaxant effect of JHE and the influence of K+ channels and Ca2+ intra- and extracellular sources on JHE-stimulated response were assessed. Results: Arteries pre-contracted with phenylephrine showed concentration-dependent relaxation (0.380 to 1.92 mg/mL). Treatment with K+ channel blockers (tetraethyl-ammonium, glibenclamide, 4-aminopyridine) hindered relaxation due to JHE. In addition, phenylephrine-stimulated contraction was hindered by previous treatment with JHE. Inhibition of sarcoplasmic reticulum Ca2+ ATPase did not change relaxation due to JHE. In addition, JHE inhibited the contraction caused by Ca2+ influx stimulated by phenylephrine and KCl (75 mM). Conclusion: JHE induces endothelium-independent vasodilation. Activation of K+ channels and inhibition of Ca2+ influx through the membrane are involved in the JHE relaxant effect.
publishDate 2016
dc.date.none.fl_str_mv 2016-09-01
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2016004200223
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2016004200223
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/abc.20160118
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia - SBC
publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia - SBC
dc.source.none.fl_str_mv Arquivos Brasileiros de Cardiologia v.107 n.3 2016
reponame:Arquivos Brasileiros de Cardiologia (Online)
instname:Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC
instname_str Sociedade Brasileira de Cardiologia (SBC)
instacron_str SBC
institution SBC
reponame_str Arquivos Brasileiros de Cardiologia (Online)
collection Arquivos Brasileiros de Cardiologia (Online)
repository.name.fl_str_mv Arquivos Brasileiros de Cardiologia (Online) - Sociedade Brasileira de Cardiologia (SBC)
repository.mail.fl_str_mv ||arquivos@cardiol.br
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