Stroke, Vol 19, 571-578, Copyright © 1988 by American Heart Association
G Sutherland, H Lesiuk, R Bose and AA Sima
The effects of mannitol, nimodipine, and indomethacin on ischemic neuronal
injury were examined in 45 rats divided equally into nine groups subjected
to 10 minutes of forebrain ischemia. Of two control groups, one received
maintenance fluids while the other received a normal saline bolus. In the
remaining seven groups, mannitol, nimodipine, and indomethacin were
administered singly or in combination 5 minutes before forebrain ischemia.
Seven days after ischemia, the brains were perfusion-fixed, sectioned
coronally into 2.8-mm slices, and stained with hematoxylin and eosin.
Ischemic neurons were directly counted on predetermined regions of
standardized serial sections. Considerable amelioration of ischemic injury
(ischemic neurons/total neurons) was observed with mannitol (ischemic
injury, 7 +/- 5% in the hippocampal CA1/CA2 sectors and 28 +/- 17% in the
CA3 sector). This is in contrast to control values of 64 +/- 11% and 80 +/-
6%, respectively, and those obtained in the normal saline group of 70 +/-
10% and 59 +/- 13%, respectively. The beneficial effect with nimodipine
reached significance in only the hippocampal CA3 sector (ischemic injury,
35 +/- 21%). Indomethacin showed no significant benefit. Combining the
agents resulted in significantly reduced neuronal injury compared with
control groups, although the effect was not greater than that achieved with
mannitol alone. The degree of ischemic injury was least when all three
agents were used in combination (ischemic injury, 12 +/- 12% in the
hippocampal CA1/CA2 sectors and 4 +/- 4% in the CA3 sector). Our data
support the concept that successfully blocking the ischemic cascade with a
single, diversely acting agent or multiple agents will evoke the best
beneficial response.
ARTICLES
Effect of mannitol, nimodipine, and indomethacin singly or in combination on cerebral ischemia in rats
Department of Pharmacology, University of Manitoba, Winnipeg, Canada.
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