Stroke, Vol 19, 1013-1019, Copyright © 1988 by American Heart Association
W Young, JC Wojak and V DeCrescito
U74006F is a member of a new family of steroid drugs called 21-
aminosteroids, which are potent inhibitors of lipid peroxidation with
little or no glucocorticoid or mineralocorticoid activity. We investigated
the effects of U74006F on the early ionic edema produced by middle cerebral
artery occlusion in rats. Intravenous doses of 3 mg/kg U74006F were given
10 minutes and 3 hours after occlusion. Tissue concentrations of Na+, K+,
and water at and around the infarct site were measured by atomic absorption
spectroscopy and by wet-dry weight measurements 24 hours after occlusion.
Compared with vehicle treatment, U74006F treatment reduced brain water
entry, Na+ accumulation, K+ loss, and net ion shift by 25-50% in most brain
areas sampled in the frontal and parietal cortex. However, reductions of
ionic edema were most prominent and reached significance (p less than
0.005, unpaired two- tailed t test) mostly in the frontoparietal and
parietal cortex areas adjacent to the infarct site. Our findings suggest
that a steroid drug without glucocorticoid or mineralocorticoid activity
can reduce edema in cerebral ischemia but that the effects are largely
limited to tissues in which collateral blood flow may be present.
ARTICLES
21-Aminosteroid reduces ion shifts and edema in the rat middle cerebral artery occlusion model of regional ischemia
Department of Neurosurgery, New York University Medical Center, New York.
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