Electrophysiologic, inotropic and antiarrhythmic effects of propafenone, 5-hydroxypropafenone and N-depropylpropafenone

G. Malfatto, A. Zaza, M. Forster, B. Sodowick, P. Danilo, M. R. Rosen

Research output: Contribution to journalArticlepeer-review

Abstract

We compared the electrophysiologic, inotropic and antiarrhythmic properties of propafenone and two metabolites, 5-hydroxy (5-OH) propafenone and N-depropyl (N-DP) propafenone. In 18 canine Purkinje fibers with normal maximum diastolic potentials, all drugs (1 x 10 -8 to 1 x 10 -5 M) reduced action potential amplitude and duration. However, propafenone and 5-OH propafenone reduced V̇(max) in a use-dependent fashion at a lower concentration than N-DP propafenone. In 16 Purkinje fibers, slow response action potentials were induced by 22 mM K + and isoproterenol, 1 x 10 -6 M. V̇(max) was comparably reduced by all compounds at 1 x 10 -5 M, but action potential amplitude was not affected by 5-OH propafenone. In 16 other Purkinje fibers in which automaticity at low levels of membrane potential was induced by BaCl 2 (0.25 mM), only 5-OH propafenone was effective in slowing the automatic rate at therapeutic concentrations (3 μg/ml). In 15 guinea pig papillary muscles, all three drugs had negative inotropic effects at concentrations ≥ 1 x 10 -6 M. In conscious dogs with sustained ventricular tachycardia 24 hr after infarction, we injected propafenone or a metabolite through an atrial cannula. At similar plasma levels, neither propafenone (n=6) nor N-DP propafenone (n=6) suppressed the arrhythmia, whereas 5-OH propafenone eliminated ventricular tachycardia in four of six dogs, and was more effective against monomorphic than polymorphic ventricular tachycardia. Hence, the two major metabolites of propafenone have important electrophysiologic effects, and 5-OH propafenone is more potent than the parent compound as a antiarrhythmic drug in the 24-hr Harris dog.

Original languageEnglish
Pages (from-to)419-426
Number of pages8
JournalJournal of Pharmacology and Experimental Therapeutics
Volume246
Issue number2
Publication statusPublished - 1988

ASJC Scopus subject areas

  • Pharmacology

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