Quantified parameters of photically evoked afterdischarge and EEG back
ground activity of visual cortex of freely moving rats were used as va
riables to obtain a t profile for each drug dosage. Behavioural scores
were also used. The determination of the dose/time-effect profile of
a compound was based on normalization of data and on calculation of th
e first two factor values in comparison with pooled data of representa
tives of neuroleptic, anxiolytic, convulsant, petit mal anticonvulsant
, antidepressant and psychostimulant drug classes. The compounds were
investigated in different dosages and/or routes of administration. The
model and procedure are validated for antipsychotic, anxiolytic and v
igilance enhancer effect, and comprise the predictability of proconvul
sive and petit mal anticonvulsive effects.