Experimental list
Figures | Purpose | Experiments | Number of mice |
---|---|---|---|
Figure 1A–F | To assess the effect of stroke and EA treatment on the synaptic activity | Electrophysiological recording in slices | GAD67-GFP mice: Sham group (N = 7), Stroke group (N = 5), and Stroke + EA group (N = 5) |
Figure 1G,H | To validated whether the tonic inhibition was changed | Electrophysiological recording in slices | 9/3* |
Figure 2A–G | To explore the expressions of PNNs in different conditions and show the injection sites of PNNs degradation and test the efficacy of injection of P-nase or ChABC | (1) Injection of P-nase or ChABC (2) Immunofluorescence | P-nase-injected group (N = 2) ChABC-injected group (N = 2) 27/3* |
Figure 3A–C | To explore the role of PNNs in the regulation of neuronal activity in the stroke or EA treatment | (1) Injection of P-nase or ChABC (2) Immunofluorescence | 18/3* |
Figure 4A–E | To explore the role of PNNs in the regulation of neuronal activity in the stroke or EA treatment | (1) Injection of P-nase or ChABC (2) In vivo electrophysiological recording | 24/4* |
Figure 5A–F | To record the sEPSCs and sIPSCs | (1) Injection of P-nase (2) Electrophysiological recording in slices | Sham group (N = 6), Stroke group (N = 4), and Stroke + EA group (N = 3) |
Figure 5A–F | To record the sEPSCs and sIPSCs | (1) Injection of ChABC (2) Electrophysiological recording in slices | Sham group (N = 6), Stroke group (N = 3) and Stroke + EA group (N = 3) |
Figure 6A,B | To validate the function of PNNs in the EA-mediated improvement of swallowing function | (1) Injection of P-nase or ChABC (2) Electromyography recording in the mylohyoid in vivo | 36/6* |
Total = 160 mice, GAD67-GFP = 17 mice, C57 = 143 mice |