Abstract

Vitamin E is localized in membranes and functions as an efficient inhibitor of lipid peroxidation in biological systems. In this study, we measured the reaction rates of vitamin E (α-, β-, γ-, δ-tocopherols, TocH) and tocol with aroxyl radical (ArO ) as model lipid peroxyl radicals in membranes by stopped-flow spectrophotometry. Egg yolk phosphatidylcholine (EYPC) vesicles were used as a membrane model. EYPC vesicles were prepared in the aqueous methanol solution (MeOH:H 2O = 7:3, v/v) that gave the lowest turbidity in samples. The second-order rate constants ( k s) for α-TocH in MeOH/H 2O solution with EYPC vesicles were apparently 3.45 × 10 5 M −1 s −1, which was about 8 times higher than that (4.50 × 10 4 M −1 s −1) in MeOH/H 2O solution without EYPC vesicles. The corrected k s of α-TocH in vesicles, which was calculated assuming that the concentration of α-TocH was 133 times higher in membranes of 10 mM EYPC vesicles than in the bulk MeOH/H 2O solution, was 2.60 × 10 3 M −1 s −1, which was one-seventeenth that in MeOH/H 2O solution because of the lower mobility of α-TocH in membranes. Similar analyses were performed for other vitamin E analogues. The k s of vitamin E in membranes increased in the order of tocol < δ-TocH < γ-TocH ∼ β-TocH < α-TocH. There was not much difference in the ratios of reaction rates in vesicles and MeOH/H 2O solution among vitamin E analogues [ k s(vesicle)/ k s (MeOH/H 2O) = 7.7, 10.0, 9.5, 7.4, and 5.1 for α-, β-, γ-, δ-TocH, and tocol, respectively], but their reported ratios in solutions of micelles and ethanol were quite different [ k s(micelle)/ k s(EtOH) = 100, 47, 41, 15, and 6.3 for α-, β-, γ-, δ-TocH, and tocol, respectively]. These results indicate that the reaction sites of vitamin E analogues were similar in vesicle membranes but depended on hydrophobicity in micelle membranes, which increased in the order of tocol < δ-TocH < γ-TocH ∼ β-TocH < α-TocH.

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