The ability of adrenergic catechol derivatives, including dobutamine,
dopamine, and isoproterenol, to inhibit lipid peroxidation was examine
d. All the catechol derivatives we tested strongly inhibited lipid per
oxidation. Dobutamine was a more powerful inhibitor of iron-catalyzed
lipid peroxidation than the other agents, suggesting that part of the
antioxidant activity of dobutamine is due to chelating iron. In additi
on, the catechol derivatives scavenged not only diphenylpicrylhydrazyl
(DPPH) free radicals, but also 2,2' azinobis-(3-ethylbenzothiazoline-
6-sulfonic acid) (ABTS) radical cations and 2,2' azobis-(2-amidinoprop
ane)-dihydrochloride (AAPH) peroxyl radicals, indicating that the anti
oxidative activities of these agents are evidently due to scavenging f
ree radicals. However, the rate constant of these catechol derivatives
in scavenging hydroxyl radicals was < 10(10) M-1 sec(-1), suggesting
that they may not protect against biological damage induced by hydroxy
l radicals. BIOCHEM PHARMACOL 55;12:2001-2006, 1998. (C) 1998 Elsevier
Science Inc.