EFFECT OF ANTIARRHYTHMIC DRUGS ON THE PREMATURE ACTION-POTENTIAL DURATION IN CANINE CARDIAC PURKINJE-FIBERS

Abstract

The effect of 6 class I antiarrhythmic drugs, i.e., quinidine (5 .mu.g/ml), disopyramide (10 .mu.g/ml), procainamide (30 .mu.g/ml), flecainide (4 .mu.g/ml), lidocaine (4 .mu.g/ml) and mexiletine (4 .mu.g/ml), on the durations of the basic action potential (APDb) at a cycle length of 500 ms and on the premature APD (APD1) elicited at progressively increasing diastolic intervals (DI) was studied in canine Purkinje fibers. The difference between APDt elicited at diastolic intervals of 100 ms and the earliest APDt elicited at the onset of effective refractory period was defined as the range of APDt. In control this range was 98 .+-. 1.8 ms (n = 59). Disopyramide and procainamide did not change the range significantly but the other 4 drugs decreased it significantly (P < 0.01) as follows: quinidine by 50.2%, lidocaine by 60.2%, mexiletine by 61.6% and flecainide by 61.4%. The following 4 factors contributed to this decrease in range of APD1: shorter duration of APDb, increased effective refractory period/APD ratio, slower kinetics of APD restitution, and shift of normalized restitution curve toward longer APDt values. The magnitude of the contribution made by each of the above factors varied with different drugs. The greatest contributing factor for quinidine was an increased effective refractory period/APD ratio, for lidocaine a slower restitution and for flecainide and mexiletine the shift of the restitution curve. Antiarrhythmic drugs belonging to the same class have different effects on the range of premature APD. These effects cannot be predicted from the effect of the drug on APDb alone.