Roberto Padrini, Mohammad Al Bunni*, Monica Mollichelli*, Antonella Alberti**, Roberto Varotto**, Pietro Maiolino*, Mariano Ferrari**.
Department of Pharmacology and Anesthesiology and
**Department of Clinical and Experimental Medicine, University of Padova, *Division of Cardiology, Cittadella Hospital, Cittadella, Italy
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Rac-sotalol is a non selective
beta-adrenoceptor blocker with the additional property of prolonging the action
potential duration and the QT interval on the surface ECG1. The most serious adverse
reaction to sotalol is polymorphic ventricular tachycardia (TdP), which is favoured by
excessive QT interval prolongation and heart rate slowing2. Various experimental
studies in cardiac myocytes3,4 and intact
animals5,6 have investigated the interaction
between sotalol and mexiletine at an electrophysiological level and found that: a)
mexiletine attenuated sotalol-induced action potential prolongation, but further
prolonged cell refractoriness; b) sotalol-mexiletine combination had additive
antiarrhythmic effect on electrically-induced ventricular tachycardia in dogs while
preventing sotalol-induced TdP. On the basis of these experimental findings, we
investigated whether mexiletine can interfere with the class III effect of sotalol also in
man, at currently used doses.
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