Document Detail


Effects of procainamide on automatic and triggered impulse initiation in isolated preparations of canine cardiac Purkinje fibers.
MedLine Citation:
PMID:  2459539     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The effects of procainamide (40 mg/L) were studied on automatic and triggered impulse initiation in isolated preparations of canine cardiac Purkinje fibers using standard microelectrode techniques. Procainamide decreased normal automaticity by 48% in Purkinje fibers superfused with standard (KCl 4 mM) Tyrode's solution. In contrast, procainamide decreased the rate of normal Purkinje fibers that had been treated with isoproterenol (1 microM) by only 6% (NS). For comparison, the effects of lidocaine (4 mg/L) and quinidine (5 mg/L) were studied on isoproterenol-treated fibers. Lidocaine and quinidine both significantly decreased the isoproterenol-enhanced rate of normal automaticity (by 45 and 10%, respectively). In studies of the effects of procainamide on Purkinje fibers with abnormal automaticity (i.e., the pacemakers had maximal diastolic potentials less than -60 mV), it was found that drug treatment decreased the rate of 24 h infarct zone Purkinje fibers by 22% and barium chloride (250 microM) treated Purkinje fibers by 51%. In studies of another five infarct zone preparations, the Purkinje fibers had maximal diastolic potentials greater than -75 mV and showed triggered activity with delayed afterdepolarizations. Procainamide decreased the triggered activity in only one of these preparations. Ventricular tachycardias that respond to procainamide may be caused by abnormal automaticity, whereas procainamide refractory tachycardias may result from triggered activity or from catecholamine-enhanced normal automaticity.
Authors:
K H Dangman
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Publication Detail:
Type:  In Vitro; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Journal of cardiovascular pharmacology     Volume:  12     ISSN:  0160-2446     ISO Abbreviation:  J. Cardiovasc. Pharmacol.     Publication Date:  1988 Jul 
Date Detail:
Created Date:  1988-11-08     Completed Date:  1988-11-08     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  7902492     Medline TA:  J Cardiovasc Pharmacol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  78-87     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, College of Physicians and Surgeons of Columbia University, New York, NY 10032.
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MeSH Terms
Descriptor/Qualifier:
Action Potentials / drug effects
Animals
Barium / pharmacology
Barium Compounds*
Chlorides*
Dogs
Heart Conduction System / drug effects*
Isoproterenol / pharmacology
Lidocaine / pharmacology
Procainamide / pharmacology*
Purkinje Fibers / drug effects*,  physiology
Quinidine / pharmacology
Grant Support
ID/Acronym/Agency:
HL-24354/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Barium Compounds; 0/Chlorides; 10361-37-2/barium chloride; 137-58-6/Lidocaine; 51-06-9/Procainamide; 56-54-2/Quinidine; 7440-39-3/Barium; 7683-59-2/Isoproterenol

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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