The effect of seizures on subsequent long-term behavior was studied in
immature rats. A similar severity of seizures were induced in 20-day
old rats (P20) and 45-day old rats (P45) by intraperitoneal injections
of pilocarpine at doses of 200 mg/kg and 380 mg/kg, respectively. Imm
ediately after injection of pilocarpine, prolonged seizures with elect
roencephalographic ictal discharges were observed in both groups of ra
ts. These seizures were followed by seemingly complete neurological re
covery. In rats that received pilocarpine at P45 spontaneous recurrent
seizures appeared after 4-10 days and persisted until completion of t
he study at P100. Behavioral tests performed when the rats were fully
mature demonstrated that they were more aggressive when handled, more
active in open field, and had deficits in learning platform position i
n the water maze as compared to controls. Furthermore, flurothyl seizu
re latency was significantly lower in pilocarpine-treated P45 rats tha
n controls. Histology examination showed gross cell loss in the CA3 su
bfield of the hippocampus in four out of six pilocarpine-treated rats
while no cell loss was found in control rats. Rats that received piloc
arpine at P20, despite having more severe seizures than the P45 rats,
had no histological lesions, did not develop spontaneous recurrent sei
zures, and had no significant difference in the flurothyl seizure late
ncy Lest when compared to their controls. While there was no differenc
e between the control and pilocarpine-treated rats in the handling and
open field test, P20 rats receiving pilocarpine were slower in learni
ng platform position in the water maze than the controls. Rats receivi
ng pilocarpine at P45 performed significantly more poorly than rats tr
eated at P20 in the water maze. These results suggest that prolonged s
eizures in immature rats can cause long-term behavioral deficits. Howe
ver, the severity and nature of these deficits are highly age dependen
t.