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. 2012 Mar 12;33(4):438–444. doi: 10.1038/aps.2011.181

Figure 1.

Figure 1

(A) Phase-contrast image showing a single patch recording from 7-d cultured hippocampal neurons for the recording of the VGCCs. Scale bar, 10 μm. (B) Pharmacological separation of the VGCC subtypes in hippocampal neurons. Upper panel, inward Ca2+ channel Ba2+ currents evoked by pulses from −60 mV to 0 mV at the times indicated in the lower panel. Lower panel, time course of effects of ω-conotoxin GVIA (1 μmol/L), ω-agatoxin IVA (30 nmol/L) and nifedipine (10 μmol/L) on the Ba2+ current amplitude.