Stroke, Vol 21, 1435-1438, Copyright © 1990 by American Heart Association
M Fisher, PH Levine and RA Cohen
Leukocytes recruited to regions of focal cerebral ischemia may contribute
to tissue injury by their ability to promote inflammation. A novel group of
drugs, the 21-aminosteroids, have been observed to reduce neurologic damage
and vasogenic cerebral edema in animal models of stroke by inhibiting lipid
peroxidation. Production of hydrogen peroxide and free radicals by
leukocytes during the inflammatory response may contribute to lipid
peroxidation and other consequences of free radical-mediated tissue injury.
We assessed the effect of U74500A, a 21-aminosteroid, on the generation of
hydrogen peroxide by and on the chemiluminescence of stimulated
polymorphonuclear leukocytes and monocytes from normal humans. U74500A
significantly reduced the generation of hydrogen peroxide by
polymorphonuclear leukocytes (p less than 0.001) and monocytes (p less than
0.01) in a dose-dependent manner. Monocyte chemiluminescence was also
significantly inhibited (p less than 0.05), but polymorphonuclear
leukocyte-associated chemiluminescence was unchanged. Our results indicate
that U74500A can reduce the concentration of oxygen metabolites associated
with stimulated human leukocytes, and this effect may explain in part how
21- aminosteroids reduce lipid peroxidation, ischemic injury, and vasogenic
edema.
ARTICLES
A 21-aminosteroid reduces hydrogen peroxide generation by and chemiluminescence of stimulated human leukocytes
Department of Neurology, Medical Center of Central Massachusetts- Memorial, Worcester 01605-2982.
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