Effects of propafenone on calcium currents in single ventricular myocytes of guinea‐pig

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Abstract
1 The effects of propafenone on the inward calcium current (ICa) were investigated in isolated single ventricular myocytes of the guinea-pig by the whole-cell clamp method. Propafenone inhibited ICa in a dose-dependent manner at concentrations of propafenone ranging from 1 × 10−8 to 1 × 10−3 m and half maximal block of ICa occurred at a propafenone concentration of 1.5 × 10−6 m. Propafenone did not change the current-voltage relation of ICa other than a reduction in amplitude and showed no clear use- or frequency-dependent effects upon ICa (stimulation frequencies from 0.03 to 2 Hz). Propafenone did not alter the steady-state inactivation process: the half maximal activation potentials were 18.5 ± 2.2 mV in the control state and 20.9 ± 5.0 mV in the presence of 1×10−6 m propafenone (n = 12, NS). Propafenone (1 × 10−6 m) increased the half-time of reactivation by 73.9% (n = 6, 212.3 ± 1.2 ms vs 369.2 ± 1.5 ms, P < 0.05). 2 We conclude that propafenone blocks ICa in a concentration-dependent and a channel state-, use- or frequency-independent manner. The ICa, blockade elicited by propafenone at clinically therapeutic plasma concentration is significant and may be involved in its anti-arrhythmic effects.

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