Abstract |
The efficacy of nimodipine in preventing ischemic brain injury was tested in rats subjected to a 20-minute period of high-grade forebrain ischemia by 4-vessel occlusion. Three minutes after restoration of circulation to the brain, an intravenous bolus of 5 micrograms/kg nimodipine or an equivalent amount of vehicle or saline was given, followed by continuous intravenous infusion of the respective solution at 1 microgram/kg/min for 2 hours. In a second series, a larger bolus (20 micrograms/kg of nimodipine) and longer infusion period (6 hours) were employed. Histopathology of the brain was evaluated blindly 72 hours later and graded on a conventional 3-point scale. There was no significant effect of treatment in either series. In the 6-hour series, the percent of cerebral hemispheres showing damage of Grades 2 or 3 in zone CA1 of the hippocampus and in the striatum, respectively, was 100 and 40% for the nimodipine-treated rats, 100 and 42% for rats receiving vehicle, and 75 and 25% for animals receiving saline. Thus, this study revealed no beneficial effect of nimodipine when given following a 20-minute period of severe forebrain ischemia.
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Authors | S Vibulsresth, W D Dietrich, R Busto, M D Ginsberg |
Journal | Stroke
(Stroke)
1987 Jan-Feb
Vol. 18
Issue 1
Pg. 210-6
ISSN: 0039-2499 [Print] United States |
PMID | 3810755
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Animals
- Brain Ischemia
(drug therapy, pathology)
- Corpus Striatum
(pathology)
- Hippocampus
(pathology)
- Male
- Neurons
(drug effects, pathology)
- Nimodipine
(therapeutic use)
- Rats
- Rats, Inbred Strains
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