Mr. Sarkisian et al., Effects of hyperthermia and continuous hippocampal stimulation on the immature and adult brain, BRAIN DEVEL, 21(5), 1999, pp. 318-325
Whether febrile seizures lead to hippocampal necrosis is a question of para
mount clinical importance, This study attempted to simulate a complex febri
le seizure, compared with hyperthermia (HYP) alone and prolonged seizure al
one (produced by continuous hippocampal stimulation (CHS)), Four groups of
rats were studied at each of two ages, immature (postnatal day, P20) and ad
ult (P60). Group I was subjected to 45 min of HYP (body temperature 40 degr
ees C) plus CHS, Group 2 received 45 min of HYP alone, Group 3 got 45 min o
f CHS alone, and Group 4 was sham-handled control rats. Baseline and post-s
ession EEGs were recorded in ail groups. Subsequently, brains were examined
histologically for evidence of hippocampal damage. Both CHS-treated groups
(with and without HYP) exhibited behavioral and EEG seizures while the gro
up undergoing HYP alone did not have seizures. There were no gross histolog
ical lesions in any group. Cell counts in regions CA1, CA3, dentate gyrus a
nd dentate hilus did not differ in rats under any condition of hyperthermia
and CHS, in either P20 or P60 rats compared to age-matched controls. These
results indicate that both immature and mature rodents are resistant to hy
perthermic brain damage and raises the question of whether febrile seizures
play a role in the genesis of mesial temporal sclerosis. (C) 1999 Elsevier
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