Purpose: This study was designed to quantify the relation between expressio
ns of NMDA receptor (NMDAR) subunits (1 and 2A/B) and the epileptogenicity
in human focal cortical dysplasia.
Methods: Immunoblotting and immunoprecipitation were used to quantify these
receptor subunits in tissue resected from EEG-verified epileptic and dista
l nonepileptic frontal cortical areas in each of three patients as determin
ed by chronic subdural electrode recordings. In each patient, adjacent sect
ions were immunostained to verify that the numbers of dysplastic neurons we
re greater in epileptic than in nonepileptic cortex.
Results: In all patients, NMDAR2A/B expressions and their coassemblies with
NMDAR1 were increased in epileptic dysplastic cortex compared with the rel
atively normal appearing nonepileptic cortex. For all three patients, there
were no significant differences in NMDAR1 protein expressions between the
two EEG groups.
Conclusions: These results suggest that increased NMDAR1-NMDAR2A/B coassemb
ly contributes to hyperexcitability in dysplastic cortical neurons and foca
l seizure onsets.