Abstract

Following the recent suggestion that oxidative damage to lipids might involve the formation of C-2 glyceryl radicals, in addition to main-chain allylic radicals, which are generally thought important, we studied the kinetics of potential ‘repair’ reactions by vitamin E and vitamin K1 (which are lipophilic and tend to locate in cell membranes) with 1,1,2-trimethylallyl and 1-acetoxyprop-2-yl radicals as models of, respectively, main-chain and glyceryl-type radicals. The second-order rate constants for the reaction between trimethylallyl radicals and vitamin E and vitamin K1 are 9.38 × 106 and 3.54 × 108 l mol−1 s−1 and those between 1-acetoxyprop-2-yl radicals and vitamin E and vitamin K1 are 1.76 × 108 and 2.03 × 106 l mol−1 s−1, respectively. The results suggest that direct scavenging of glyceryl radicals by vitamin E should be an efficient process, and of main-chain allylic radicals fairly so. Additionally, it appears that vitamin K1 can act directly as a ‘radical repair agent,’ given its relatively high reactivity with allylic radicals (four times faster than with vitamin E), so prior reduction to the quinol form may be unnecessary. Copyright © 2000 John Wiley & Sons, Ltd.

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