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. Author manuscript; available in PMC: 2022 Feb 3.
Published in final edited form as: J Neural Eng. 2021 Jan 25;18(1):10.1088/1741-2552/abc29c. doi: 10.1088/1741-2552/abc29c

Figure 8.

Figure 8.

Mesoscale imaging of neuronal calcium response to ICMS shows distant inhibition during both 10 Hz patterns. (A) Representative images of the neuronal calcium response to 10 Hz-Burst and Uniform stimulation patterns. Images are shown as an average of fluorescence intensity over the baseline period, the dF/F0 from 0–2 s of stimulation, 28–30 s of stimulation, and 3–5 s post-stimulation, and the mean dF/F0 over the entire 30 s stimulation train. See supplemental movies 79 for activation over time. (B) Similar to the two-photon neuropil imaging, there is loss of activity over the 30 s stimulation train proximal to the electrode for 100 Hz stimulation. Interestingly, there in regions beyond the 2P imaging window (>250 μm), there was also loss of activity for over the stimulation train for both 10 Hz groups (significant two-way ANOVA effect for TP: p < 0.001). (C) Further, mean dF/F0 over the stimulation train (0–30 s) as a function of distance from the electrode shows distant inhibition for both 10 Hz stimulation patterns., but not the 100 Hz pattern. Two-way ANOVA confirms that there is a statistically significant difference between the patterns and over distance (p < 0.0001), with [I^ indicating a significant difference between the 10 Hz-Burst pattern and 100 Hz patterns within 0–60 μm of the electrode (p < 0.05). Additionally, * and ** indicate significant differences between the 0–60 μm bin and indicated bins (p < 0.05, p < 0.001, respectively. Color indicates the pattern of comparison). Data is presented as mean ± SEM, with n = 4 stimulation trials from a total of 3 different animals.