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. 2018 Jul 18;38(29):6513–6526. doi: 10.1523/JNEUROSCI.0674-18.2018

Figure 3.

Figure 3.

GIRK modulators affect mature GC intrinsic properties. A, Current injections (top, 500 ms) and voltage responses (bottom) in GCs with the indicated intracellular solution and Ba2+ (500 μm) or ML297 (10 μm). Right, ML297 had no effect on GCs from GIRK2 KO mice. Dotted + and − lines represent mean values from GTP+ and GTP conditions shown in Figure 1, respectively. B–D, Individual (red) and mean (black) values of RMP (B), input resistance (C), and rheobase (D) recorded in GCs perfused with Ba2+ (GTP+) or ML297 (GTP+, GTP, and GIRK2 KO mice). ANOVA: F(5,50) = 62.28, F(5,51) = 49.69, and F(5,50) = 42.26 for B–D, respectively. Bonferroni's post hoc test: ***p < 0.001; **p < 0.01; *p < 0.05; $ indicate differences against GTP+ pool; # indicate differences against GTP. E, Number of APs evoked by increasing current injections measured over 500 ms after perfusing ML297 in WT and GIRK2 KO GCs (n = 8 and 6, respectively). F, Representative currents (held at −70 mV) −70 mV) evoked by Ba2+ or ML297 using a GTP+ intracellular solution. G, The effect of Ba2+ or ML297 (open symbols) on outward currents (I holding) using the indicated internal solutions and GIRK2 KO mice. Dotted + and − lines represent mean standing outward current from 15 GCs using GTP+ intracellular (18 ± 2 pA) and 11 GCs using GTP intracellular solution (4 ± 0.7 pA). Paired t test, ***p < 0.001. Single symbols represent the mean ± SEM and individual paired values are connected with lines.