Perinatal hypoxia is associated with both seizures arising acutely and
the subsequent development of temporal lobe epilepsy (as determined r
etrospectively). We therefore attempted to identify acute and chronic
morphological and/or electrophysiological hippocampal pathologies asso
ciated with experimentally induced hypoxia in immature rats. Pups were
exposed to 15 minutes of hypoxia on 3 successive days (starting on po
stnatal day 8; P8), or to 60 minutes of hypoxia on P10 with either one
or multiple hypoxia-induced seizures. For animals experiencing multip
le seizures, flurothyl seizure threshold was significantly lower than
that of controls at 60 to 80 days, but not at 10 days, after hypoxia.
Acutely, there was a treatment-related increase in the number and the
density of pyknotic dentate and hilar neurons, in particular in animal
s experiencing multiple seizures. However, 60 to 80 days after the mul
tiple-seizure protocol, the number of dentate and hilar neurons did no
t differ between control and experimental animals. Electrophysiologica
l measures of pyramidal cell properties showed no striking difference
between experimental and control animals at any time point. These resu
lts indicate that early postnatal hypoxia and hypoxia-induced seizure
episodes decrease seizure threshold in the adult but produce minimal a
cute or chronic morphological or functional changes in the hippocampus
.