Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

Stark, U; Stark, G; Stoschitzky, K; Pilger, E; Nagl, S; Lindner, W; Tritthart, HA.
Stereoselective electrophysiological effects of propafenone in Langendorff perfused guinea pig hearts.
Basic Res Cardiol. 1992; 87(1):87-97 Doi: 10.1007/BF00795393
Web of Science PubMed FullText FullText_MUG Google Scholar

 

Co-Autor*innen der Med Uni Graz
Pilger Ernst
Stoschitzky Kurt
Tritthart Helmut
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
The present study was focused on the stereoselective electrophysiological effects of (R)- and (S)-propafenone.HCl evaluated in isolated Langendorff perfused guinea pig hearts. Conduction intervals were measured using an ECG-recording method of high resolution. Refractory periods of the different parts of the myocardium were determined by stimulation with premature stimuli, as well as by stimulation with increasing pacing rate (rate-dependent/refractory periods). Drug concentrations of 0.1, 1 and 3 microM were tested. Both compounds induced a dose-dependent increase in AV-nodal, His-bundle, and intraventricular conduction time which reached significance (p less than 0.01) following 3 microM of either compound. Sinus rate was also dose-dependently and significantly reduced. (R)- and (S)-propafenone.HCl induced a marked prolongation of the rate-dependent refractory period of sino-atrial (by 140 +/- 22%, p less than 0.01 and by 141 +/- 14%, p less than 0.01, respectively) and AV-nodal (by 34 +/- 22%, p less than 0.01 and by 42 +/- 15%, p less than 0.01, respectively) conduction and of the atrial (by 182 +/- 21%, p less than 0.01 and by 195 +/- 15%, p less than 0.01, respectively) and ventricular (by 93 +/- 16%, p less than 0.01 and by 88 +/- 16%, p less than 0.01, respectively) myocardium. The effective refractory periods evaluated by stimulation with premature stimuli were also significantly prolonged under the influence of (R)- and (S)-propafenone.HCl, except the ventricular myocardial refractoriness by (R)-propafenone.HCl (increase to 114 +/- 23%, n.s.). Both compounds showed a strong rate-dependence of their effects and, thus, the refractory periods evaluated by stimulation with increasing pacing rate were significantly more prolonged than the refractory periods evaluated by stimulation with premature stimuli. The main difference between the effects of (R)- and (S)-propafenone.HCl on the cardiac electrical activity is the lack of effect of (R)-propafenone.HCl on the ventricular myocardial refractoriness evaluated by stimulation with premature stimuli.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Cardiac Pacing, Artificial -
Coronary Circulation -
Electrophysiology -
Female -
Guinea Pigs -
Heart - drug effects
Heart Conduction System - drug effects
Heart Rate - drug effects
Male - drug effects
Propafenone - pharmacology
Refractory Period, Electrophysiological - pharmacology
Reserpine - pharmacology
Stereoisomerism - pharmacology

Find related publications in this database (Keywords)
Propafenone-HCl
Enantiomers
Cardiac Conduction and Refractoriness
Isolated Guinea Pig Heart
Langendorff Perfused
© Med Uni Graz Impressum