By using the whole cell voltage-clamp technique, we studied changes in plas
ma membrane permeability at different meiotic stages of bovine oocytes. Fol
licular oocytes were matured in vitro and activated by Ca2+ ionophore. Oocy
tes at germinal vesicle (GV), germinal vesicle breakdown (GVBD), metaphase
I (MI), metaphase II (MII), and meiosis exit were used for electrophysiolog
ical recording. By clamping the oocytes at -30 mV, we found that the L-type
voltage-dependent Ca2+ channels were active at the GV stage and that their
activity decreased after the GVBD stage. Furthermore, the resting potentia
l decreased from the GV to the MI stage and increased again at MII. A signi
ficant decrease of the steady-state conductance occurred from the GV to the
MI stage, followed by a sharp increase at the MII stage. With the addition
of organic L- type Ca2+ channel blockers (nifedipine and verapamil), we in
hibited the Ca2+ currents. However, only in the case of verapamil was there
a decrease of in vitro maturation efficiency. Our results suggest that, in
addition to the cumulus-oocyte junctions, the plasma membrane channels pro
vide another mode of Ca2+ entry into bovine oocytes during meiosis.