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. 2018 Jan 10;8:3. doi: 10.1038/s41398-017-0060-z

Fig. 3.

Fig. 3

Persistent bursting in neonatal PCP-treated rats underlies abnormal spatiotemporal activity propagation. a PCP treatment increases spatial activity propagation specifically by increasing repeat (rather than new) neuronal activations. Branching parameter measured in number of neurons (total, new, and repeat) for different treatment groups. b Schematic representation of spatiotemporal activity propagation in SAL vs. PCP treated rats. Empty triangles represent quiescent neurons; filled triangles, active neurons; arrows, activity propagation. The black cascade shows a representative pattern of feedforward activity; in PCP treated rats, aberrant repeat activity (red triangles) caused by persistent bursting is superimposed on this cascade. c PCP-treated rats show shallower distributions in burst lengths. Left, distributions of burst lengths for different treatment groups. Distributions were plotted after pooling all bursts per movie, then averaged. Right, slope exponents for burst length distributions for different treatment groups. d PCP treatment leads to more persistent bursts of activity. Fraction of bursts with length greater than one frame for different treatment groups. e Removing persistent bursts rescues the PCP-induced increase in pairwise cross-correlation. Complementary cumulative distributions of pairwise cross-correlations for SAL, PCP, and PCP with repeat activations removed. Distributions were plotted for each movie per group then averaged. f KS distance, power law exponent, and branching parameter for PCP, and PCP with repeat activations removed. Error bars indicate s.e.m; *, P < 0.05, **, P < 0.01, ***, P < 0.001