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Stroke, Vol 22, 1259-1264, Copyright © 1991 by American Heart Association
KS Deluga, FB Plotz and AL Betz
BACKGROUND AND PURPOSE: Repetitive periods of cerebral ischemia result in
more severe injury than a single period of ischemia of similar total
duration. We investigated the possibility of prostaglandin mediation of
this increased injury by attempting to modify brain edema formation with
indomethacin pretreatment. METHODS: Under halothane/N2O anesthesia, groups
of gerbils underwent bilateral carotid occlusion to induce forebrain
ischemia. Group I underwent a single 15-minute period of carotid occlusion.
Group II underwent three 5-minute periods of occlusion at hourly intervals.
Groups III and IV were similar to groups I and II, respectively, but
received 0.2 mg/kg indomethacin before carotid occlusion. Cortical and
cerebellar water and sodium contents were determined in control animals (n
= 6) at time zero and in experimental animals 24, 48, and 72 hours after
ischemia (n = 6-10 gerbils/group at each time point). RESULTS: Cortical
water and sodium contents in group II peaked 48 hours after insult (82.15
+/- 0.31% and 420 +/- 14 meq/kg dry wt, respectively) and were
significantly higher than control and group I values at both 24 and 48
hours. Cortical water did not change from control in group I animals.
Indomethacin pretreatment significantly attenuated increases in water and
sodium content seen at 48 hours in gerbils undergoing repetitive ischemia
(peak 80.02 +/- 0.45% and 300 +/- 39 meq/kg dry wt), but did not affect
mortality. CONCLUSIONS: Indomethacin lessens edema after repetitive
cerebral ischemia, suggesting that elevations of cyclooxygenase products
are responsible, at least in part, for severe brain edema following
repetitive ischemia.
ARTICLES
Effect of indomethacin on edema following single and repetitive cerebral ischemia in the gerbil
Department of Pediatrics, University of Michigan, Ann Arbor.
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