Both (-)-verapamil and (+)-verapamil caused cardiodepression and inverted the positive force-frequency staircase in human ventricular tissue while allosterically inhibiting calcium channel binding.
The similar potency ratios for binding and cardiodepression suggest a common locus of action for verapamil enantiomers within the calcium channel.
Ventricular preparations from patients with mitral disease and hypertrophic obstructive cardiomyopathy (HOCM) were set up to contract isometrically. Ventricular membrane particles were also prepared and putative calcium channels were labelled with 3H-nimodipine. Positive staircase was induced by varying the rate of stimulation of isolated strips from 6 min-1 to 120 min-1 in the presence of 6-60 microM (-)-adrenaline or (-)-noradrenaline. (-)-Verapamil 3-5 microM or (+)-verapamil 20-30 microM reversed the force-frequency relationship (i.e. caused negative staircase) in preparations from patients with mitral disease or HOCM. In subendocardial strips of ventricular septum from 5 patients with HOCM paced at 60 min-1, both (-)-verapamil and (+)-verapamil caused cardiodepression. Half-maximal cardiodepression was observed with 0.4 microM (-)-verapamil and with 3 microM (+)-verapamil. 3H-nimodipine bound to ventricular membrane particles in a saturable, reversible fashion to a high affinity site with an equilibrium dissociation constant of 0.23 nM. The density of these sites was 95 fmol mg-1 of membrane protein. Binding of the tritiated 1,4-dihydropyridine was stereoselectively inhibited by 1,4-dihydropyridine enantiomers and nifedipine. (-)-Verapamil and (+)-verapamil inhibited high affinity 3H-nimodipine binding in a negative heterotropic allosteric manner with (-)-verapamil being 5 times more potent than (+)-verapamil on an IC50 basis. At a given 3H-nimodipine concentration, (+)-verapamil inhibited a greater fraction of specific 3H-nimodipine binding. The allosteric mode of (+)-verapamil inhibition of 3H-nimodipine binding was confirmed by kinetic studies. (-)-Verapamil shifted (+)-verapamil-binding inhibition curves to the right in an apparently competitive fashion. The inversion of staircase caused by both verapamil enantiomers suggests that they cause a use-dependent channel blockade. The similar potency ratios for binding and for cardiodepression are indicative of a common locus of action for both verapamil enantiomers within the calcium channel.
Ferry et al. (Mon,) conducted a other in Mitral valve disease and hypertrophic obstructive cardiomyopathy (n=12). Verapamil enantiomers ((-)-verapamil and (+)-verapamil) vs. Baseline (no verapamil) was evaluated on Cardiodepression and [3H]-nimodipine binding inhibition. Both (-)-verapamil and (+)-verapamil caused cardiodepression and inverted the positive force-frequency staircase in human ventricular tissue while allosterically inhibiting calcium channel binding.