E. Nagababu et N. Lakshmaiah, INHIBITION OF XANTHINE OXIDASE-XANTHINE-IRON MEDIATED LIPID-PEROXIDATION BY EUGENOL IN LIPOSOMES, Molecular and cellular biochemistry, 166(1-2), 1997, pp. 65-71
The effect of eugenol on xanthine oxidase (XO) xanthine(X)-Fe+3-ADP me
diated lipid peroxidation was studied in liver microsomal lipid liposo
mes. Eugenol inhibited the lipid peroxidation in a dose dependent mann
er as assessed by formation of thiobarbituric acid reactive substances
. When tested for its effect on XO activity per se, (by measuring uric
acid formation) eugenol inhibited the enzyme to an extent of 85% at 1
0 mu m concentration and hence formation of O-2-radical-anion also How
ever, the concentration of eugenol required for XO inhibition was more
in presence of metal chelators such as EDTA, EGTA and DETAPAC, but no
t in presence of deferoxamine, ADP and citrate. The antiperoxidative e
ffect of eugenol was about 35 times more and inhibition of XO was abou
t 5 times higher as compared to the effect of allopurinol. Eugenol did
not scavenge O-2-radical-anion generated by phenazine methosulfate an
d NAD but inhibited propagation of peroxidation catalyzed by Fe2+ EDTA
and lipid hydroperoxide containing liposomes. Eugenol inhibits XO-X-F
e3+ ADP mediated peroxidation by inhibiting the XO activity per se in
addition to quenching various radical species.