Cardiac effects of norbormide and verapamil were compared in single ventricular myocytes, right atria, and Langendorff perfused hearts isolated from guinea‐pigs.

In ventricular myocytes, norbormide 50 μm inhibited the peak calcium current (I_Ca) by 49.6±3.9% without altering the shape of the current‐voltage relationship; verapamil 1 μm inhibited I_Ca by 83.2±3.3%. Neither norbormide nor verapamil affected I_Ca at the first beat after a 3 min quiescence period; during repeated depolarizations, both drugs cumulatively blocked I_Ca (use‐dependence), with time constants of 23.0±7.0 s for norbormide and 91.3±8.4 s for verapamil.

In constant‐flow perfused hearts electrically driven at 2.5 Hz or 3.3 Hz, both norbormide and verapamil concentration‐dependently decreased ventricular contractility (dP/dt_max), atrio‐ventricular (AV) conduction velocity and coronary pressure. Intraventricular conduction velocity was slightly decreased by norbormide but not by verapamil. At an equivalent change in AV conduction, norbormide depressed heart contractility less than verapamil. The effects of norbormide on AV conduction, intraventricular conduction, and contractility were frequency‐dependent. Furthermore, the curves correlating the mechanical and electrical effects of norbormide at the two frequencies used were apparently coincident, while those of verapamil were clearly separated.

In spontaneously beating right atria, norbormide and verapamil decreased the frequency of sinus node (SA) in a concentration‐dependent way. At an equivalent effect on the AV conduction, norbormide exerted a greater effect on sinus frequency than verapamil.

These results indicate that in guinea‐pig heart norbormide has the pharmacological profile of a Ca‐antagonist with strong electrophysiological properties. In comparison with verapamil, norbormide is more selective on SA and AV node tissues and exerts a weaker negative inotropic effect on ventricles. In principle, this pattern of effects may be an advantage in treating supraventricular tachyarrhythmias in patients with heart failure. The effect of norbormide on intraventricular conduction may represent an additional antiarrhythmic mechanism.