We have evaluated the abilities of ferulic acid, (+/-) catechin, (+) c
atechin and (-) epicatechin to scavenge the reactive oxygen species hy
droxyl radical (OH.), hypochlorous acid (HOCl) and peroxyl radicals (R
O2.). Ferulic acid tested at concentrations up to 5 mM inhibited the p
eroxidation of phospholipid liposomes. Both (+/-) and (+) catechin and
(-) epicatechin were much more effective. All the compounds tested re
acted with trichloromethyl peroxyl radical (CCl3O2.) with rate constan
ts > 1 x 10(6) M-1 s-1. A mixture of FeCl3-EDTA, hydrogen peroxide (H2
O2) and ascorbic acid at pH 7.4, has often been used to generate hydro
xyl radicals (OH.) which are detected by their ability to cause damage
to the sugar deoxyribose. Ferulic acid, (+) and (+/-) catechin and (-
) epicatechin inhibited deoxyribose damage by reacting with OH. with r
ate constants of 4.5 x 10(9) M-1 s-1, 3.65 x 10(9) M-1 s-1, 2.36 x 10(
9) M-1 s-1 and 2.84 x 10(9) M-1 s-1 respectively. (-) Epicatechin, fer
ulic acid and the(+) and (+/-) catechins exerted pro-oxidant action, a
ccelerating damage to DNA in the presence of a bleomycin-iron complex.
On a molar basis, ferulic acid was less effective in causing damage t
o DNA compared with the catechins. A mixture of hypoxanthine and xanth
ine oxidase generates O2 radical anion which reduces cytochrome c to f
errocytochrome c. (+) Catechin and (-) epicatechin inhibited the reduc
tion of cytochrome c in a concentration dependent manner. Ferulic acid
and (+/-) catechin had only weak effects. All the compounds tested we
re able to scavenge hypochlorous acid at a rate sufficient to protect
alpha-1-antiproteinase against inactivation. Our results show that cat
echins and ferulic acid possess antioxidant properties. This may becom
e important given the current search for ''natural'' replacements for
synthetic antioxidant food additives.