An electrophysiological comparison of a novel class Ic antiarrhythmic agent, NIK-244 (ethacizin) and flecainide in canine ventricular muscle

British Journal of Pharmacology
H SatohK Hashimoto

Abstract

1. Electrophysiological effects of NIK-244 (ethacizin), a novel class I antiarrhythmic drug, were compared with flecainide in canine ventricular muscle by use of conventional microelectrode techniques. 2. At concentrations of 10(-6) M or higher, NIK-244 depressed the maximum rate of rise of depolarization (Vmax) significantly in a concentration-dependent manner. Also, the resting potential was depolarized at 10(-5) M. NIK-244 did not have any effect on the other action potential parameters or on the effective refractory period. 3. Flecainide significantly decreased Vmax at 3 x 10(-6) M or higher and the resting potential was depolarized at 10(-5) M. Like NIK-244, flecainide did not affect other action potential parameters. 4. NIK-244 and flecainide caused a use-dependent block of Vmax, and the rates of onset of inhibition at 3 Hz stimulation were 0.014 +/- 0.002 AP-1 at 2 x 10(-6) M NIK-244 and 0.021 +/- 0.012 AP-1 at 10(-5) M flecainide. Under the same conditions, the time constants of the recovery from use-dependent block were 27.1 +/- 13.3 s and 12.2 +/- 2.5 s for NIK-244 and flecainide, respectively. 5. These results suggest that NIK-244, like flecainide, should be classified as a slow kinetic drug and as Ic.

References

Nov 14, 1977·Biochimica Et Biophysica Acta·L M Hondeghem, B G Katzung
Jun 1, 1988·Journal of Molecular and Cellular Cardiology·K R Courtney
May 1, 1986·Naunyn-Schmiedeberg's Archives of Pharmacology·H Satoh, K Hashimoto
Nov 1, 1980·Journal of Molecular and Cellular Cardiology·K R Courtney

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