Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 1990;21:1435-1438

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fisher, M.
Right arrow Articles by Cohen, R. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fisher, M.
Right arrow Articles by Cohen, R. A.

Stroke, Vol 21, 1435-1438, Copyright © 1990 by American Heart Association


ARTICLES

A 21-aminosteroid reduces hydrogen peroxide generation by and chemiluminescence of stimulated human leukocytes

M Fisher, PH Levine and RA Cohen
Department of Neurology, Medical Center of Central Massachusetts- Memorial, Worcester 01605-2982.

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.


This article has been cited by other articles:


Home page
Pharmacol. Rev.Home page
R. F. Villa and A. Gorini
Pharmacology of Lazaroids and Brain Energy Metabolism: A Review
Pharmacol. Rev., March 1, 1997; 49(1): 99 - 136.
[Abstract] [Full Text] [PDF]