The effect of mibefradil, a new nondihydropyridine Ca2+ channel antagonist,
was investigated on Y1 cells which exhibited T-and L-type Ca2+ currents. I
n the great majority of these cells, mibefradil rapidly and selectively blo
cked T-type Ca current in a dose-dependent manner with a half maximum actio
n at 10-7 M. Furthermore, the specific L-type Ca2+ channel inhibitor, nifed
ipine, blocked the Ca2+ inward current remaining after the action of mibefr
adil. Mibefradil does not modify the voltage-dependent characteristics of t
he current/voltage relationship. However, mibefradil is more effective at d
epolarized membrane potential.