Supplementary Figure 5: Supporting data from in vivo Ca2+ imaging experiments from CeAHtr2a neurons. | Nature Neuroscience

Supplementary Figure 5: Supporting data from in vivo Ca2+ imaging experiments from CeAHtr2a neurons.

From: Central amygdala circuits modulate food consumption through a positive-valence mechanism

Supplementary Figure 5

a, Cre-dependent GCaMP6s expression in the CeA of an Htr2a-Cre;tdTomato mouse (representative of 3 mice). b, Activity of CeAHtr2a::GCaMP6s neurons increased during eating compared to baseline period (n = 69 cells across 4 mice, two-tailed unpaired t test: t(68) = 2.52, P = 0.0141). Connected points are responses of individual neurons. c, Histogram of preference indices of individual neurons for feeding during all food eating bouts. d, Example cells from two mice that reduced activity during eating. Grey bars= eating bouts. e, Mean Ca2+ responses of cells classified as Down cells (n = 9/69 cells) before and upon eating onset of all recorded feeding bouts. f, Mean Ca2+ activity of cells that reduced activity during feeding compared to baseline (n = 9 cells across 4 mice, two-tailed unpaired t test: t(8) = 3.91 P = 0.0045). Connected points are the average responses of all classified cells during individual bouts. g, Ca2+ responses of representative cells averaged across 12 FR1 trials (Upper) (total n = 36 cells from 3 mice). Lower= Ca2+ responses of the individual trials. h, Population Ca2+ responses of all recorded neurons (n = 36 cells from 3 mice) aligned to eating bout end. Upper = mean. Lower = heat map of normalized Ca2+ responses from all neurons. Each row is one trial.

Bar graph values are mean ± SEM. * P < 0.05, ** P < 0.01. Scale bar: 50 μm.

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