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. 2010 Jun 23;104(3):1347–1354. doi: 10.1152/jn.00098.2010

Fig. 5.

Fig. 5.

Ca2+ channel currents in isolated ganglion cells were reduced by L-803,087. A: examples of Ca2+ channel currents recorded from an isolated ganglion cell under voltage-clamp in the absence (left) and presence (right) of L-803,087 (10 nM). Voltage command protocol shown below. B: mean data show that administration of L-803,087 significantly reduced Ca2+ channel current at intermediate membrane potentials (n = 4; *P < 0.05, 2-way repeated-measures ANOVA vs. control). C: in the absence of L-803,087, administration of Ca2+ channel blockers, NIF (10 μM) and ω-conotoxin GVIA (CTX, 1 μM) reduced Ca2+ channel currents compared with control recordings (recorded at −10 mV, n = 3–4 cells/group). D: following administration of NIF, L-803,087 had no additional blocking effect on Ca2+ channel current, whereas following administration of CTX, L-803,087 further reduced Ca2+ channel current (−10 mV, n = 3–7 cells/group; **P < 0.05, ANOVA vs. L-803,087).