Epilepsy research using positron emission tomography (PET) has provide
d considerable new information about ictal and interictal dysfunctions
in human epilepsy. Neuroreceptor mapping with PET ligands has reveale
d altered central benzodiazepine receptor and opiate receptor densitie
s in partial epilepsies interictally, and regional increases in endoge
nous opioid peptide concentrations during absence seizures. Imaging of
perfusion and glucose metabolism during cognitive processing has show
n interictal abnormalities of regional activation in partial and gener
alized epilepsies. The diagnostically robust patterns of interictal gl
ucose hypometabolism are not adequately explained by macrostructural a
nd microstructural alterations in temporal lobe epilepsy. Current inve
stigations of the pathophysiology of interictal hypometabolism must ad
dress ultrastructural and neurochemical factors. Clinical PET in pre s
urgical evaluation of medically refractory epilepsies remains an activ
e area of research, but remarkably little antiepileptic drug research
has exploited PET techniques.