The study was designed to determine which type of cell death occurs fo
llowing kindling induced seizures, and to determine which neurons die.
For this purpose seizures were kindled from the entorhinal cortex. Fo
llowing a range of 5-85 stage 5 seizures, rats were sacrificed, and th
e tissue was prepared for analysis. The TUNEL and silver impregnation
methods were used to identify apoptotic or necrotic cell death, respec
tively. These methods were subsequently combined with immunocytochemis
try, to determine if diseased neurons expressed somatostatin or the NM
DA receptor (NMDAR1). The tissue analysis demonstrated that following
kindling induced seizures. 1) hippocampal and extrahippocampal neurons
die, 2) some neurons die through apoptosis, others through necrosis,
and 3) some of the diseased neurons express somatostatin, others the N
MDAR1 and that both subpopulations of neurons are present at hippocamp
al and extrahippocampal sites.