The relationship between excitation and inhibition. A, Electrical 3D maps show N2b amplitude before and after application of 10 μm bicuculline. Bicuculline disinhibited several areas. The distribution and intensity of the inhibitory effect is demonstrated by the subtraction map (control − bicuculline). B, In the same slice shown in A, the number of electrodes measuring a detectable N2b response after bicuculline application (black dots) is increased. Note that N2a was already measurable over the electrodes showing N2b after bicuculline application (large open dots). C, Left, Plot of N2b changes caused by bicuculline as a function of N2a amplitude. The plot reveals a strong negative correlation between the parameters. The thick line is a monoexponential fitting to the whole dataset [y = y0 + A × exp(−x/τ), with y0 = 95, x0 = 0, A = 1174, τ = 0.09; p(χ2) < 0.001; R2 = 0.72; n = 180 in 7 slices], the thin dashed lines are fittings to single-slice data (always R2 > 0.6). Right, Plot of N2b versus N2a initial amplitude from the same slices: note the absence of correlation. For each slice, N2a and N2b amplitudes are normalized to their maximum control value. D, The histogram shows the average change caused by bicuculline in the electrodes with a local peak of excitation versus the surrounding ones. The effect of bicuculline is stronger in the surround (n = 60 from 7 slices; *p < 0.03, paired t test). No comparable difference is observed by random sampling the granular layer electrodes and measuring the surrounding activity (n = 60 from 7 slices; p = 0.74, paired t test). Error bars indicate SEM.