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Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve

BACKGROUND: The aim of the present work was to characterize the electrophysiological effects of the non-steroidal anti-inflammatory drug diclofenac and to study the possible proarrhythmic potency of the drug in ventricular muscle. METHODS: Ion currents were recorded using voltage clamp technique in...

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Autores principales: Kristóf, Attila, Husti, Zoltán, Koncz, István, Kohajda, Zsófia, Szél, Tamás, Juhász, Viktor, Biliczki, Péter, Jost, Norbert, Baczkó, István, Papp, Julius Gy, Varró, András, Virág, László
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534043/
https://www.ncbi.nlm.nih.gov/pubmed/23300901
http://dx.doi.org/10.1371/journal.pone.0053255
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author Kristóf, Attila
Husti, Zoltán
Koncz, István
Kohajda, Zsófia
Szél, Tamás
Juhász, Viktor
Biliczki, Péter
Jost, Norbert
Baczkó, István
Papp, Julius Gy
Varró, András
Virág, László
author_facet Kristóf, Attila
Husti, Zoltán
Koncz, István
Kohajda, Zsófia
Szél, Tamás
Juhász, Viktor
Biliczki, Péter
Jost, Norbert
Baczkó, István
Papp, Julius Gy
Varró, András
Virág, László
author_sort Kristóf, Attila
collection PubMed
description BACKGROUND: The aim of the present work was to characterize the electrophysiological effects of the non-steroidal anti-inflammatory drug diclofenac and to study the possible proarrhythmic potency of the drug in ventricular muscle. METHODS: Ion currents were recorded using voltage clamp technique in canine single ventricular cells and action potentials were obtained from canine ventricular preparations using microelectrodes. The proarrhythmic potency of the drug was investigated in an anaesthetized rabbit proarrhythmia model. RESULTS: Action potentials were slightly lengthened in ventricular muscle but were shortened in Purkinje fibers by diclofenac (20 µM). The maximum upstroke velocity was decreased in both preparations. Larger repolarization prolongation was observed when repolarization reserve was impaired by previous BaCl(2) application. Diclofenac (3 mg/kg) did not prolong while dofetilide (25 µg/kg) significantly lengthened the QT(c) interval in anaesthetized rabbits. The addition of diclofenac following reduction of repolarization reserve by dofetilide further prolonged QT(c). Diclofenac alone did not induce Torsades de Pointes ventricular tachycardia (TdP) while TdP incidence following dofetilide was 20%. However, the combination of diclofenac and dofetilide significantly increased TdP incidence (62%). In single ventricular cells diclofenac (30 µM) decreased the amplitude of rapid (I(Kr)) and slow (I(Ks)) delayed rectifier currents thereby attenuating repolarization reserve. L-type calcium current (I(Ca)) was slightly diminished, but the transient outward (I(to)) and inward rectifier (I(K1)) potassium currents were not influenced. CONCLUSIONS: Diclofenac at therapeutic concentrations and even at high dose does not prolong repolarization markedly and does not increase the risk of arrhythmia in normal heart. However, high dose diclofenac treatment may lengthen repolarization and enhance proarrhythmic risk in hearts with reduced repolarization reserve.
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spelling pubmed-35340432013-01-08 Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve Kristóf, Attila Husti, Zoltán Koncz, István Kohajda, Zsófia Szél, Tamás Juhász, Viktor Biliczki, Péter Jost, Norbert Baczkó, István Papp, Julius Gy Varró, András Virág, László PLoS One Research Article BACKGROUND: The aim of the present work was to characterize the electrophysiological effects of the non-steroidal anti-inflammatory drug diclofenac and to study the possible proarrhythmic potency of the drug in ventricular muscle. METHODS: Ion currents were recorded using voltage clamp technique in canine single ventricular cells and action potentials were obtained from canine ventricular preparations using microelectrodes. The proarrhythmic potency of the drug was investigated in an anaesthetized rabbit proarrhythmia model. RESULTS: Action potentials were slightly lengthened in ventricular muscle but were shortened in Purkinje fibers by diclofenac (20 µM). The maximum upstroke velocity was decreased in both preparations. Larger repolarization prolongation was observed when repolarization reserve was impaired by previous BaCl(2) application. Diclofenac (3 mg/kg) did not prolong while dofetilide (25 µg/kg) significantly lengthened the QT(c) interval in anaesthetized rabbits. The addition of diclofenac following reduction of repolarization reserve by dofetilide further prolonged QT(c). Diclofenac alone did not induce Torsades de Pointes ventricular tachycardia (TdP) while TdP incidence following dofetilide was 20%. However, the combination of diclofenac and dofetilide significantly increased TdP incidence (62%). In single ventricular cells diclofenac (30 µM) decreased the amplitude of rapid (I(Kr)) and slow (I(Ks)) delayed rectifier currents thereby attenuating repolarization reserve. L-type calcium current (I(Ca)) was slightly diminished, but the transient outward (I(to)) and inward rectifier (I(K1)) potassium currents were not influenced. CONCLUSIONS: Diclofenac at therapeutic concentrations and even at high dose does not prolong repolarization markedly and does not increase the risk of arrhythmia in normal heart. However, high dose diclofenac treatment may lengthen repolarization and enhance proarrhythmic risk in hearts with reduced repolarization reserve. Public Library of Science 2012-12-31 /pmc/articles/PMC3534043/ /pubmed/23300901 http://dx.doi.org/10.1371/journal.pone.0053255 Text en © 2012 Kristóf 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
Kristóf, Attila
Husti, Zoltán
Koncz, István
Kohajda, Zsófia
Szél, Tamás
Juhász, Viktor
Biliczki, Péter
Jost, Norbert
Baczkó, István
Papp, Julius Gy
Varró, András
Virág, László
Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve
title Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve
title_full Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve
title_fullStr Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve
title_full_unstemmed Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve
title_short Diclofenac Prolongs Repolarization in Ventricular Muscle with Impaired Repolarization Reserve
title_sort diclofenac prolongs repolarization in ventricular muscle with impaired repolarization reserve
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534043/
https://www.ncbi.nlm.nih.gov/pubmed/23300901
http://dx.doi.org/10.1371/journal.pone.0053255
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