Stroke, Vol 19, 997-1002, Copyright © 1988 by American Heart Association
ED Hall, KE Pazara and JM Braughler
U74006F (21-[4-(2,6-di-1-pyrrolidinyl-4-pyrimidinyl)-1-piperazinyl]-16
alpha-methylpregna-1,4,9(11)-triene-3,20-dione, monomethane sulfonate) is a
novel and potent inhibitor of central nervous system tissue lipid
peroxidation that is devoid of classical steroid hormonal activities. Its
possible efficacy in attenuating postischemic mortality and neuronal
necrosis was examined in gerbils following 3-hour unilateral carotid artery
occlusion. Male Mongolian gerbils received two intraperitoneal injections
of either vehicle or U74006F (3 or 10 mg/kg), the first injection 10
minutes before and the second injection at the end of the 3-hour ischemic
episode. In an initial series of experiments, vehicle-treated gerbils
displayed 60.9% (14 of 23) survival 24 hours after ischemia, which
decreased to 34.8% (8 of 23) at 48 hours. In contrast, the 10 mg/kg
U74006F-treated group showed 86.7% (13 of 15) survival at 24 hours (p less
than 0.15 vs. vehicle) and 80.0% (12 of 15) survival at 48 hours (p less
than 0.02). In a second series, neurons in the hippocampal CA1 subfield and
the medial and lateral cerebral cortex were counted in gerbils surviving 24
hours after unilateral carotid artery occlusion. Comparison of neuronal
densities in the ischemic hemisphere with those in the contralateral
nonischemic hemisphere revealed significant neuronal preservation in all
three brain regions of 10 mg/kg i.p. x 2 U74006F-treated gerbils. Our
results show that U74006F can improve survival and attenuate neuronal
necrosis in a severe brain ischemia model.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
21-Aminosteroid lipid peroxidation inhibitor U74006F protects against cerebral ischemia in gerbils
Central Nervous System Disease Research Unit, Upjohn Company, Kalamazoo, Michigan 49001.
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