Limbic P300 potentials can be recorded within the mesial temporal robes of
patients with temporal lobe epilepsy (TLE). To delineate possible mechanism
s of their generation and pathological alteration, we analysed limbic P300s
in 55 TLE patients with and 29 without Ammon's horn sclerosis (AHS) and co
rrelated their amplitudes with neuronal cell counts in 30 histopathological
specimens. Limbic P300 amplitudes were reduced on the side of the epilepto
genic focus only in patients with AHS. Moreover, in AHS patients, limbic P3
00 latencies were prolonged bilaterally; and in patients with left-sided AH
S, amplitudes were reduced bilaterally. Both findings suggest bilateral fun
ctional deficits in TLE with unilateral AHS. Limbic P300 areas correlated s
ignificantly with neuronal densities of dentate gyrus granule cells but not
hippocampal pyramidal cells in the CA1-4 (cornu ammonia) subfields. This f
inding points to a potential mechanism for the bilateral effects of unilate
ral AHS as both dentate gyri exhibit strong reciprocal contralateral connec
tivity.