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Proarrhythmic effects of the class III agent almokalant: importance of infusion rate, QT dispersion, and early afterdepolarisations

Proarrhythmic effects of the class III agent almokalant: importance of infusion rate, QT... Abstract Objective: The aim was to study factors contributing to torsade de pointes in the acquired long QT syndrome. Methods: Anaesthetised rabbits or cats were given a continuous infusion of methoxamine and the class III agent almokalant (at a rate of 5 or 25 nmol·kg−1·min−1, respectively) and the effects on incidence of torsade de pointes and QT dispersion were examined. Effects of almokalant on action potentials recorded from Purkinje fibres and ventricular cells of rabbits and cats were also studied. Results: “High rate” infusion of almokalant prolonged the QT, interval [from 162(SEM 6.2) ms to 211(5.3) ms, p<0.001] and initiated torsade de pointes in 9/10 rabbits after a dose of 391(116.3) nmol·kg−1. During “low rate” infusion, 1/8 rabbits developed torsade de pointes (p = 0.0029) despite infusion of 900 nmol·kg−1 almokalant and QTC prolongation from 162(3.6) ms to 230(12.6) ms (p<0.01). In eight separate rabbits given the high rate infusion of almokalant, seven developed torsade de pointes and the QTC dispersion increased from 15(1.7) ms to 32(5.6) ms (p<0.05). In six rabbits given the low rate infusion, none developed torsade de pointes (p = 0.0023), and the QTC dispersion was unaltered. In six cats, high rate infusion induced a QT interval lengthening from 241(6.0) ms to 349(8.0) ms (p<0.001), but in only one cat was torsade de pointes initiated and preceded by a marked increase in QT dispersion (from 22 ms to 78 ms). In vitro, almokalant caused a marked lengthening of the action potential duration and early afterdepolarisations in Purkinje fibres but not in ventricular muscle cells of the rabbit. In the cat, however, almokalant induced a homogeneous prolongation of the action potential duration in both cell types, and early afterdepolarisations were never observed. Conclusions: The rate of infusion of repolarisation delaying agents may influence the dispersion of repolarisation and play a decisive role in the initiation of torsade de pointes. Cardiovascular Research 1993;27:2186-2193 acquired long QT syndrome, torsade de pointes, tachyarrhythmias, rabbit, cat This content is only available as a PDF. Copyright © 1993, European Society of Cardiology http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Cardiovascular Research Oxford University Press

Proarrhythmic effects of the class III agent almokalant: importance of infusion rate, QT dispersion, and early afterdepolarisations

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Publisher
Oxford University Press
Copyright
Copyright © 1993, European Society of Cardiology
ISSN
0008-6363
eISSN
1755-3245
DOI
10.1093/cvr/27.12.2186
Publisher site
See Article on Publisher Site

Abstract

Abstract Objective: The aim was to study factors contributing to torsade de pointes in the acquired long QT syndrome. Methods: Anaesthetised rabbits or cats were given a continuous infusion of methoxamine and the class III agent almokalant (at a rate of 5 or 25 nmol·kg−1·min−1, respectively) and the effects on incidence of torsade de pointes and QT dispersion were examined. Effects of almokalant on action potentials recorded from Purkinje fibres and ventricular cells of rabbits and cats were also studied. Results: “High rate” infusion of almokalant prolonged the QT, interval [from 162(SEM 6.2) ms to 211(5.3) ms, p<0.001] and initiated torsade de pointes in 9/10 rabbits after a dose of 391(116.3) nmol·kg−1. During “low rate” infusion, 1/8 rabbits developed torsade de pointes (p = 0.0029) despite infusion of 900 nmol·kg−1 almokalant and QTC prolongation from 162(3.6) ms to 230(12.6) ms (p<0.01). In eight separate rabbits given the high rate infusion of almokalant, seven developed torsade de pointes and the QTC dispersion increased from 15(1.7) ms to 32(5.6) ms (p<0.05). In six rabbits given the low rate infusion, none developed torsade de pointes (p = 0.0023), and the QTC dispersion was unaltered. In six cats, high rate infusion induced a QT interval lengthening from 241(6.0) ms to 349(8.0) ms (p<0.001), but in only one cat was torsade de pointes initiated and preceded by a marked increase in QT dispersion (from 22 ms to 78 ms). In vitro, almokalant caused a marked lengthening of the action potential duration and early afterdepolarisations in Purkinje fibres but not in ventricular muscle cells of the rabbit. In the cat, however, almokalant induced a homogeneous prolongation of the action potential duration in both cell types, and early afterdepolarisations were never observed. Conclusions: The rate of infusion of repolarisation delaying agents may influence the dispersion of repolarisation and play a decisive role in the initiation of torsade de pointes. Cardiovascular Research 1993;27:2186-2193 acquired long QT syndrome, torsade de pointes, tachyarrhythmias, rabbit, cat This content is only available as a PDF. Copyright © 1993, European Society of Cardiology

Journal

Cardiovascular Research – Oxford University Press

Published: Dec 1, 1993

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