Characteristics of Ca2+ currents in 3-month-old SGNs from apical and basal turns of the cochlea, and the effects of Ca2+ current blockers. A, Family of inward Ca2+ currents from apical SGN elicited from a holding potential of −70 mV to step potentials from −50 to 30 mV in 10 mV increments (left, inset). A similar voltage pulse protocol was applied to generate Ca2+ current traces from basal SGNs (right, inset). Peak Ca2+ current density–voltage relations for apical (•) and basal (○) SGNs. At voltages (−10–10 mV), there were significant differences between apical and basal Ca2+ current densities (*p < 0.05; n = 17). B, The DHP antagonist, nimodipine, blocks a component of whole-cell Ca2+ currents in SGNs. Current traces recorded from neurons isolated from apical [top, inset (control); bottom, inset (nimodipine)] segments of the cochlea. Perfusion of external solution containing 10 μm nimodipine resulted in a reduction of the Ca2+ currents. The corresponding current density–voltage relations for apical (B) and basal (C) SGNs (n = 9). The control data are illustrated with black lines and symbols and the residual current after nimodipine block is shown in blue lines and symbols. D–I, The current density–voltage relations were generated before (black lines and symbols) and after (blue lines and symbols) application of Ca2+ current blockers: rSNX-482 for R-type currents (D, E); ATX for P/Q-type currents (F, G); and CTX for N-type currents (H, I). D, E, Current density–voltage relations for control (black) and the remaining current density after application of toxins (blue) for apical (D) and basal (E) SGNs (n = 6). The insets in the left panels of the plots are representative current traces recorded from a holding voltage of −70 mV to a step voltage of 0 mV. F, G, Similar data obtained upon recording control Ca2+ currents and after application of the P/Q-type Ca2+ current blocker, 1 μm ATX. H, I, Summary data of the effects of the N-type Ca2+ channel blocker on apical versus basal neurons. Table 1 illustrates the summary data for the effects of Ca2+ channel blockers on whole-cell Ca2+ currents.