Circulation, Vol 76, 1380-1387, Copyright © 1987 by American Heart Association
WE Cascio, JR Foster, JW Buchanan Jr, TA Johnson and LS Gettes
Procainamide, a type 1A antiarrhythmic drug, blocks sodium channels and
reduces the maximum rate of rise of the cardiac action potential (Vmax) in
a rate-dependent fashion. In vitro, the magnitude of this rate- dependent
reduction in Vmax is greater in tissue that is partially depolarized at
rest than in tissue with a normal resting potential. Reductions in Vmax
produced by drugs that block sodium channels are also directly related to
the reductions in longitudinal conduction velocity of action potential
propagation in papillary muscle preparations. We therefore sought to
determine whether the rate- dependent conduction slowing induced by
procainamide in the intact canine heart is enhanced in myocardial tissue
abnormally depolarized by an elevated myocardial extracellular potassium
concentration, [K+]o. QRS duration and epicardial activation times were
measured as indexes of myocardial conduction. QRS duration and epicardial
activation times were measured at control (4.0 mM) and at intermediate (6.5
mM) and high (9.2 mM) myocardial [K+]o in the presence or absence of a
clinically relevant procainamide concentration (12.2 +/- 2.6 g/ml) at the
longest obtainable interstimulus interval of 440 msec and at 330, 280, and
250 msec. Intermediate and high myocardial [K+]o alone induced rate-
dependent conduction slowing as the frequency of stimulation increased
(cycle length 440 msec to 330, 280, and 250 msec). In the presence of
procainamide, rate-dependent conduction slowing was observed at all levels
of myocardial [K+]o, and the amount of rate-dependent change in conduction
time increased as the myocardial [K+]o was increased.(ABSTRACT TRUNCATED AT
250 WORDS)
ARTICLES
Enhancement of procainamide-induced rate-dependent conduction slowing by elevated myocardial extracellular potassium concentration in vivo
Department of Medicine, University of North Carolina at Chapel Hill 27599.
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