Skip to main content
. 2016 Jan 26;26(4):1778–1794. doi: 10.1093/cercor/bhw002

Figure 4.

Figure 4.

Faster propagation of focal ictal discharges in slices from Scn1a−/+ mice. (A) Schematic of the experimental configuration for the generation of focal ictal discharges. (B) Representative voltage-clamp recordings at −50 mV of an NMDA-induced ictal event in a pyramidal neuron 1 mm away from the NMDA application site in a WT (top) and a Scn1a−/+ (bottom) mouse. (C) Left: average delays of ictal onset in pyramidal neurons from WT (N = 24 ictal events from 11 mice) and Scn1a−/+ (N = 38 ictal events from 12 mice) animals in the presence of 4-AP. Right: average delays of ictal onset in pyramidal neurons from WT (N = 8 ictal events from 2 mice) and Scn1a−/+ (N = 9 ictal events from 2 mice) animals in low Mg2+ (0 Mg2+). (D) Average values of ictal onset delay normalized to control in 4-AP (N = 38 ictal events from 12 mice) and low Mg2+ (N = 9 ictal events from 2 mice).