Liochev S I, Fridovich I
Institute of Physiology, Bulgarian Academy of Sciences, Sofia.
Free Radic Biol Med. 1989;6(6):617-22. doi: 10.1016/0891-5849(89)90069-5.
Vanadate stimulates the oxidation of NAD(P)H by biological membranes because such membranes contain NAD(P)H oxidases which are capable of reducing dioxygen to O2- and because vanadate catalyzes the oxidation of NAD(P)H by O2-, by a free radical chain mechanism. Dihydropyridines, such as reduced nicotinamide mononucleotide (NMNH), which are not substrates for membrane-associated NAD(P)H oxidases, are not oxidized by membranes plus vanadate unless NAD(P)H is present to serve as a source of O2-. When [NMNH] greatly exceeds [NAD(P)H], in such reaction mixtures, one can observe the oxidation of many molecules of NMNH per NAD(P)H consumed. This reflects the chain length of the free radical chain mechanism. We have discussed the mechanism and significance of this process and have tried to clarify the pertinent but confusing literature.
钒酸盐可刺激生物膜对NAD(P)H的氧化,这是因为此类膜含有能够将双原子氧还原为超氧阴离子的NAD(P)H氧化酶,还因为钒酸盐可通过自由基链式机制催化超氧阴离子对NAD(P)H的氧化。二氢吡啶类物质,如还原型烟酰胺单核苷酸(NMNH),它们不是膜相关NAD(P)H氧化酶的底物,除非有NAD(P)H作为超氧阴离子的来源,否则不会被膜加钒酸盐氧化。当[NMNH]大大超过[NAD(P)H]时,在此类反应混合物中,可以观察到每消耗一分子NAD(P)H,就有许多分子的NMNH被氧化。这反映了自由基链式机制的链长。我们已经讨论了该过程的机制和意义,并试图澄清相关但令人困惑的文献。