Circulation, Vol 75, 265-271, Copyright © 1987 by American Heart Association
M Talajic, MR DeRoode and S Nattel
It has been suggested that some of the effects of long-term amiodarone
therapy may be due to accumulation of a metabolite, desethylamiodarone. To
evaluate the pharmacologic actions of the metabolite, we gave single
intravenous doses (10 or 25 mg/kg) of amiodarone or desethylamiodarone to
anesthetized dogs. The resulting plasma and myocardial concentrations of
both agents were similar to levels achieved with long- term oral amiodarone
therapy in man. Amiodarone and desethylamiodarone produced
frequency-dependent slowing in ventricular and atrioventricular nodal
conduction and increased atrial and ventricular refractory periods. The
relative effects of these agents on fast- and slow-channel tissues
differed, with amiodarone producing significantly greater prolongation of
Wenckebach cycle length and desethylamiodarone producing larger increases
in QRS duration, atrial refractory period, and ventricular refractory
period. We conclude that desethylamiodarone has substantial
electrophysiologic effects at clinically relevant concentrations and has
relatively greater effect on fast-channel tissue in vivo than does
amiodarone. The accumulation of desethylamiodarone probably accounts for
some of the delayed electrophysiologic effects in patients receiving
long-term treatment with amiodarone.
ARTICLES
Comparative electrophysiologic effects of intravenous amiodarone and desethylamiodarone in dogs: evidence for clinically relevant activity of the metabolite
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