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[Preprint]. 2024 Nov 9:2024.11.09.622790. [Version 1] doi: 10.1101/2024.11.09.622790

Figure 3. SV and LDCV release from CGRPPBel neurons are driven by differing frequencies.

Figure 3.

(A) Schematic of monitoring LDCV and SV releases from the CGRPPBel→CeAl terminals in vivo. PBel neurons were stimulated using a bipolar tungsten electrode.

(B) LDCV release signals during electrical stimulation of the PBel area (left) and quantification of AUC data (right). (N = 4 mice, average of 3–4 repeats).

(C) SV release signals during electrical stimulation of the PBel area (left) and quantification of AUC data (right). (N = 4 mice, average of 3 repeats).

(D) Schematic of experiment.

(E) Image of a patch-clamped CeAl neuron, surrounded by perisomatic mCherry signals. Scale?

(F) Optically evoked EPSCs are abolished by CNQX treatment. Scale bar, 50 μs, 50 pA.

(G) Post-synaptic current responses evoked by a train of photostimulation at 4 Hz or 40 Hz. Scale bar: 100 ms, 20 pA (top); 20 ms, 20 pA (bottom).

(H) Fidelity of oEPSCs in response to 4-Hz and 40-Hz photostimulation.

(I) Example trace of a CeAl neurons membrane potential in response to 4-Hz or 40-Hz photostimulation. Scale bar: 30 s, 2 mV.

(J) Quantification of membrane potential responses to 4-Hz or 40-Hz photostimulation.

****P < 0.0001, **P < 0.01, *P < 0.05. Data are presented as mean ± s.e.m.