Key result
Fendiline reduces +Vmax and APD20 in guinea pig papillary muscles, indicating Na+ and Ca2+ channel block.
Why the study?
Does fendiline alter action potential configuration and conduction velocity in guinea pig papillary muscle?
Does fendiline alter action potential configuration and conduction velocity in guinea pig papillary muscle?
Fendiline exhibits frequency-dependent block of Na+ and Ca2+ channels in guinea pig papillary muscle, leading to inhibition of fast and slow conduction.
Remains preclinical; leaves open whether frequency-dependent Na+/Ca2+ blockade confers antiarrhythmic effects in intact models.
The action of fendiline on cardiac electrical activity was investigated in guinea pig papillary muscle by monitoring frequency- and time-dependent changes in membrane potential, action potential (AP) configuration and conduction velocity. Isolated guinea pig papillary muscles driven at 0.1 to 3 Hz showed a concentration-dependent reduction of +Vmax, overshoot, and AP duration at -20mV (APD20) in the presence of fendiline (1-320 microM), reflecting inhibition of Na+ and L-type Ca2+ channels, respectively. No significant change in resting potential and AP duration at 90% repolarization (APD90) were observed. Inhibition of +Vmax and APD20 was more prominent at higher frequency of stimulation (2 Hz) than at lower ones (0.2 Hz), demonstrating frequency-dependent block of Na+ and Ca2+ channels including an open channel block. A good relationship between changes in +Vmax and APD20 suggested some commonality in the mechanism of inhibition of Na+ and Ca2+ channels by fendiline. Time-dependence of effects of fendiline, observed in presence of bolus dose (200 microM), showed an earlier onset of inhibition of +Vmax and APD20, particularly at higher frequencies. Missed beats and conduction block also appeared earlier in preparations driven at higher frequency. These findings suggest a frequency-dependent (and open channel) block of Na+ and Ca2+ channels by fendiline, leading to inhibition of fast and slow conduction in addition to its reported inactivated Ca2+ channel block.
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Gautam et al. (2000) studied this question. Fendiline was evaluated on Changes in membrane potential, action potential configuration (+Vmax, overshoot, APD20, APD90) and conduction velocity. Fendiline produced a concentration- and frequency-dependent reduction of +Vmax and APD20 in guinea pig papillary muscles, indicating open channel block of Na+ and Ca2+ channels.
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