We found that ticlopidine, at therapeutically relevant concentrations
(2.5-10 mu M), but not aspirin nor salicylate, significantly counterac
ted copper-driven human LDL oxidation, Ticlopidine, at 5 and 10 mu M,
was also antioxidant on peroxyl radical-induced LDL oxidation; yet it
was ineffectual an thiol and ascorbate oxidation mediated by peroxyl r
adicals themselves, suggesting that drug antioxidant capacity is someh
ow related to the lipoprotein nature of the oxidizable substrate, but
not to radical scavenging, The drug could not indeed react with the st
able free radical 1,1-diphenyl-2-pycrylhydrazyl, nor had apparent meta
l complexing-inactivating activity, Thus, ticlopidine has antioxidant
effects on LDL oxidation, which, together with its anti-platelet activ
ity, could confer peculiar antiatherogenic properties to the drug in v
ivo. (C) 1998 Federation of European Biochemical Societies.