Nitric oxide-induced oxidation of α-tocopherol

Article abstract of DOI:10.1016/0968-0896(96)00191-5

Exposure of α-tocopherol (α-T) to nitric oxide under aerobic conditions resulted in a complex oxidation process whose final outcome was dictated by the nature of the reaction medium. In a cyclohexane solution, a prevailing route led to a mixture of relatively unstable polar products positive to Griess reagent. On standing at room temperature these were partially converted to the novel 2,3-dimethyl-4-acetyl-4-hydroxy-5-nitroso-2-cyclopentenone derivative. Reaction of α-T via a secondary oxidation path led to the formation of α-tocopherylquinone (α-TQ) as well as of little amounts of the corresponding nitrite ester. A quite different product pattern was observed when the reaction was carried out on a suspension of α-T in 0.1 M phosphate buffer, pH 7.4. Besides a significant formation of α-TQ and its nitrite ester, product analysis revealed a characteristic pattern of apolar compounds consisting of a yellow dimer and a series of related oligomers. These results provide an improved chemical background to inquire into the role of α-T in nitric oxide-induced tissue injury.