Hodnick W F, Milosavljević E B, Nelson J H, Pardini R S
Department of Chemistry, University of Nevada-Reno 89557.
Biochem Pharmacol. 1988 Jul 1;37(13):2607-11. doi: 10.1016/0006-2952(88)90253-5.
We have investigated the redox behavior of a series of structurally related flavonoids employing cyclic voltammetry under physiological conditions. The flavonoids that auto-oxidized and produced oxygen radicals had oxidation potentials (E 1/2) significantly lower [-30 to +60 mV vs (SCE)] than those that did not undergo auto-oxidation (+130 to +340 mV vs SCE). The range of E 1/2 values for the auto-oxidizable flavonoids was comparable to the E 1/2 range reported for the optimum quinone induced production of superoxide (O2 pi) in mitochondrial NADH-CoQ reductase (complex I). The most potent flavonoid inhibitors of mitochondrial succinate-CoQ reductase (complex II) possessed hydroxyl configurations capable of supporting redox reactions. For a series of 3,5,7-trihydroxyflavones that differed by b-ring hydroxylation it was found that decreasing E 1/2 of the flavonoids was associated with decreasing I50 values towards succinoxidase. These findings suggest that the electrochemical properties of the flavonoids may contribute to their biological activity.
我们在生理条件下采用循环伏安法研究了一系列结构相关的黄酮类化合物的氧化还原行为。自动氧化并产生氧自由基的黄酮类化合物的氧化电位(E1/2)[相对于饱和甘汞电极(SCE)为-30至+60 mV]明显低于未发生自动氧化的黄酮类化合物(相对于SCE为+130至+340 mV)。可自动氧化的黄酮类化合物的E1/2值范围与线粒体NADH-CoQ还原酶(复合体I)中醌诱导超氧化物(O2π)最佳产生所报道的E1/2范围相当。线粒体琥珀酸-CoQ还原酶(复合体II)最有效的黄酮类抑制剂具有能够支持氧化还原反应的羟基构型。对于一系列因B环羟基化而不同的3,5,7-三羟基黄酮,发现黄酮类化合物E1/2的降低与对琥珀酸氧化酶的I50值降低有关。这些发现表明,黄酮类化合物的电化学性质可能有助于其生物活性。