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Vol. 283, Issue 1, 148-156, 1997
Quebec Heart Institute, Laval Hospital and Faculty of Pharmacy,
Laval University, Sainte-Foy, Quebec, Canada
Indapamide is a diuretic agent with direct electrophysiological effects
on ionic currents involved in cardiac repolarization. In particular,
indapamide blocks the slow component of delayed rectifier potassium
current. In contrast, most class III antiarrhythmic agents, such as
dl-sotalol, block the rapid component of delayed rectifier
potassium current. Computer simulations have suggested potentiation of
drug effects on cardiac repolarization by the combined block of the
rapid component of delayed rectifier potassium current and the slow
component of delayed rectifier potassium current. Therefore, the
objective of our study was to evaluate the modulation of cardiac
electrophysiological effects of dl-sotalol by indapamide.
Two indices of cardiac repolarization, monophasic action potential
duration at 90% repolarization and effective refractory period, at two
basic cycle lengths (800 and 400 msec) were determined in 24 anesthetized open-chest dogs. In two treatment groups
(n = 6/group), data were obtained at base line and
every 2 min during steadily increasing concentrations of
dl-sotalol (0-40 µg/ml) either alone or in the presence
of indapamide (500 ng/ml). Data were also obtained in dogs receiving
either a low-dose (500 ng/ml) or a high-dose (up to 7.5 µg/ml)
infusion regimen of indapamide alone. Administration of
dl-sotalol was associated with concentration-dependent
increases in monophasic action potential duration at 90%
repolarization and effective refractory period, whereas repolarization
was only slightly altered by the administration of indapamide alone.
However, concentration-response curves of dl-sotalol were
shifted to the left in dogs treated with the combination of
dl-sotalol and indapamide, and the EC50 values
of dl-sotalol estimated for the prolongation of monophasic
action potential duration at 90% repolarization and effective
refractory period were decreased 3-fold during the coadministration of
both drugs (P < .05 vs. dl-sotalol alone). Thus, under
conditions of normal K+ levels, clinically relevant
concentrations of indapamide modulate dl-sotalol effects on
cardiac repolarization. Additional block of cardiac K+
currents, especially the rapid component of delayed rectifier potassium
current and the slow component of delayed rectifier potassium current
could explain these observations.
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