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. 2022 Jun 16;13:3167. doi: 10.1038/s41467-022-30828-0

Fig. 6. Cerebellar LTD is induced by direct activation of the mGlu1 mutant by dA-CBC.

Fig. 6

a A schematic diagram illustrating the experimental set-up. Conjunctive stimulus [PF/ΔV-stim, 30× (PF stimuli plus Purkinje cell depolarization) at 1 Hz] was applied to induce LTD at PF–Purkinje cell synapses (LTD-stim). An orientation of stimulus and recording electrodes and stimulus conditions are shown. b Averaged data of LTD recordings from mGlu1+/+ (black circles) and mGlu1CBC/CBC (red circles). Insets, representative PF-EPSC traces just before (blue; t = −1 min) and 30 min after (black and red) LTD-stim in mGlu1+/+ and mGlu1CBC/CBC mice, respectively. A right graph shows a cumulative probability of the degree of LTD at t = 30 min. [n = 7 cells from 4 mice (mGlu1+/+) or 6 cells from 4 mice (mGlu1CBC/CBC)]. c, d Averaged data of DHPG-induced (c) or Pd(sulfo-bpy)-induced (d) chemLTD recordings from mGlu1+/+ (black circles), mGlu1CBC/CBC (red circles) and mGlu1CBC/+ (green circles in d) mice. Insets, representative PF-EPSC traces just before (blue; t = −1 min) and 25 min after (black, red, or green) drug washout in each mouse group. A right graph shows a cumulative probability of the degree of LTD at t = 35 min. [n = 7 cells from 4 mice (mGlu1+/+) or 8 cells from 5 mice (mGlu1CBC/CBC) in c and n = 8 cells from 5 mice (mGlu1+/+), 11 cells from 6 mice (mGlu1CBC/CBC) or 8 cells from 5 mice (mGlu1CBC/+) in d]. Data are presented as mean ± s.e.m.