Evaluation of the timing of flecainide administration and ischemia-inducedventricular arrhythmias in rats

Citation
M. Shimizu et al., Evaluation of the timing of flecainide administration and ischemia-inducedventricular arrhythmias in rats, CURR THER R, 60(1), 1999, pp. 37-44
Citations number
24
Categorie Soggetti
Pharmacology,"Pharmacology & Toxicology
Journal title
CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL
ISSN journal
0011393X → ACNP
Volume
60
Issue
1
Year of publication
1999
Pages
37 - 44
Database
ISI
SICI code
0011-393X(199901)60:1<37:EOTTOF>2.0.ZU;2-Q
Abstract
Ischemia-induced arrhythmias are major complications of acute myocardial in farction; therefore, understanding the proper use of antiarrhythmic drugs i n this situation is important. The goal of the present study was to determi ne how the timing of flecainide administration influenced ischemia-induced arrhythmias in an isolated rat heart model. Ischemia-induced arrhythmia was produced by ligating the left coronary artery. The effect of flecainide (1 0(-6) M) on ischemia-induced arrhythmia varied depending on the time of dru g administration in relation to the time of coronary artery ligation, Drug administration both before and after (group 5) coronary artery ligation was most effective, followed by administration before (group 4) and then by ad ministration after (group 3). At the end of each experiment, the left and r ight ventricular walls of each heart were separated, and drug concentration in each part was measured. Drug concentration in the left ventricular wall differed significantly between the group in which coronary artery ligation was not performed (group 1) and group 3 or 4, No correlation between drug concentration in the right ventricular wall and antiarrhythmic effect was o bserved. These differences in antiarrhythmic effect depending an the timing of drug administration may be caused by the difference in drug concentrati on in the ischemic zone and the effect of coronary artery occlusion on the speed of drug dispersion within this zone. This myocardial infarction model is useful for studying the correlation between antiarrhythmic effect and r egional drug distribution.