Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries

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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Main Authors: Andrade,Daniela Medeiros Lobo de, Borges,Leonardo Luis, Torres,Ieda Maria Sapateiro, Conceição,Edemilson Cardoso da, Rocha,Matheus Lavorenti
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Cardiologia - SBC 2016
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2016004200223
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spelling oai:scielo:S0066-782X20160042002232016-10-05Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated ArteriesAndrade,Daniela Medeiros Lobo deBorges,Leonardo LuisTorres,Ieda Maria SapateiroConceição,Edemilson Cardoso daRocha,Matheus Lavorenti Jabuticaba (Myrciaria Cauliflora) Trees Vasodilatation Calcium Channels Muscle, Smooth Vascular 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.info:eu-repo/semantics/openAccessSociedade Brasileira de Cardiologia - SBCArquivos Brasileiros de Cardiologia v.107 n.3 20162016-09-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2016004200223en10.5935/abc.20160118
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libraryname SciELO
language English
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author Andrade,Daniela Medeiros Lobo de
Borges,Leonardo Luis
Torres,Ieda Maria Sapateiro
Conceição,Edemilson Cardoso da
Rocha,Matheus Lavorenti
spellingShingle Andrade,Daniela Medeiros Lobo de
Borges,Leonardo Luis
Torres,Ieda Maria Sapateiro
Conceição,Edemilson Cardoso da
Rocha,Matheus Lavorenti
Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
author_facet Andrade,Daniela Medeiros Lobo de
Borges,Leonardo Luis
Torres,Ieda Maria Sapateiro
Conceição,Edemilson Cardoso da
Rocha,Matheus Lavorenti
author_sort Andrade,Daniela Medeiros Lobo de
title Jabuticaba-Induced Endothelium-Independent Vasodilating Effect on Isolated Arteries
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
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.
publisher Sociedade Brasileira de Cardiologia - SBC
publishDate 2016
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2016004200223
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