C. Marie et al., NEUROLOGIC AND CYTOLOGIC OUTCOME FOLLOWING REPEATED ISCHEMIA - EFFECTOF PENTOBARBITAL, Brain research bulletin, 35(2), 1994, pp. 161-166
We examined clinical recovery from repeated brain ischemic insults tha
t have been reported to affect cytologic outcome. Brain ischemia was i
nduced in the rat by four-vessel occlusion. A 30-min ischemia was give
n as a single insult or induced in animals made ischemic 24 h earlier
by a 10-min insult but exempt both of brain hypoperfusion and neurolog
ic deficit in spite of a partial necrosis of the CA1 sector: of hippoc
ampus. Repeated ischemia was associated with a significantly poorer cl
inical outcome as indicated by an increase in percentage of rats that
exhibited postischemic seizure activity combined with the percentage o
f unconvulsive rats exhibiting neurologic deficits after 72 h of reper
fusion (81% vs. 50% after a single 30-min ischemia). Examination of hi
ppocampal damage showed that neurons surviving the first ischemia did
not acquire resistance to the second ischemia. Pentobarbital given fro
m start of overt seizures (30 to 60 mg/kg, IP, thrice daily) was able
to stop convulsions and to antagonize processes involved in ischemia-i
nduced neuronal death of CAI hippocampus.