The effects of the phenylalkylamines verapamil, gallopamil, and devapamil on L-type
calcium currents (I Ca) were studied in ventricular myocytes from rat hearts using the whole …

The voltage dependence and the kinetics of block by verapamil of L-type calcium current (I
Ca) were investigated in ventricular myocytes from rat hearts using the whole-cell patch …

Both L-and T-type calcium channels are present in the heart. In cardiac myocytes L-type
calcium channels are blocked by the classical calcium channel blockers, while T-type …

The phosphodiesterase inhibitors 3-isobutyl-1-methylxanthine (IBMX; 100 microM) and
papaverine (100 microM) increased peak L-type Ca current (ICa) more than fivefold in a way …

The influence of semotiadil fumarate, a novel vasoselective Ca2+ channel antagonist with a
benzothiazine skeleton, was measured on the high-threshold Ca2+ current ICa, L in guinea …

Abstract Effects of extracellular applications of different types of Ca 2+ channel blocking
agents (Mn 2+, verapamil, and nisoldipine) on action-potential duration and membrane …

The effects of the phenylalkylamines verapamil (V), gallopamil (G), and devapamil (D) and
their corresponding quaternary derivatives on the transient outward current (I to) were …

Whole cell experiments were used to study whether the L-type and the T-type Ca channel in
guinea-pig ventricular myocytes are blocked similarly by verapamil and flunarizine. The L …

The effect of 20 mmextracellularly applied 2, 3-Butanedione monoxime (BDM) onl-type
Ca2+ channel charge movement current was studied in whole-cell voltage-clamped guinea …

1. The whole‐cell voltage‐clamp technique was applied to isolated rat ventricular myocytes
to investigate the effects of D600 (10 (‐9)‐10 (‐3) M) on the intracellular calcium …