Cossins E, Lee R, Packer L
Department of Molecular and Cell Biology, University of California, Berkeley 94720-3200, USA.
Biochem Mol Biol Int. 1998 Jul;45(3):583-97. doi: 10.1080/15216549800202982.
The effect of various flavonoids upon the ascorbate radical lifetime was investigated by ESR spectroscopy. The radical was generated via the reaction between ascorbic acid and ascorbate oxidase, the ascorbate radical being detected. The inclusion of the flavonoids in the ascorbic acid-ascorbate oxidase reaction mixture affected both the initial intensity of the ascorbate radical and its lifetime. Of the natural sources tested, Pycnogenol prolonged the ascorbate radical lifetime to the greatest extent, from a control value of 20 min to a maximum of 80 min with 200 micrograms/ml Pycnogenol. The flavonoids could either be regenerating ascorbic acid from ascorbate, or interacting with ascorbate oxidase, thus preventing ascorbic acid binding. When p-cresol, a known ascorbate oxidase inhibitor was added to the ascorbic acid-ascorbate oxidase reaction mixture, the ascorbate radical signal intensity was dramatically reduced and did not display the time-dependent decay observed with the flavonoids. This indicates that a direct interaction between the flavonoids and ascorbate radical occurs. Some of the flavonoids tested; myricetin, polyphenon and theaflavin appeared to compete with ascorbic acid for ascorbate oxidase, as they displayed saturation behaviour. By modifying the experimental conditions the myricetin radical was detected, thus confirming the direct interaction between myricetin and ascorbate oxidase.
通过电子自旋共振光谱法研究了各种黄酮类化合物对抗坏血酸自由基寿命的影响。自由基通过抗坏血酸与抗坏血酸氧化酶之间的反应产生,并对抗坏血酸自由基进行检测。在抗坏血酸 - 抗坏血酸氧化酶反应混合物中加入黄酮类化合物,会影响抗坏血酸自由基的初始强度及其寿命。在所测试的天然来源中,碧萝芷(Pycnogenol)最大程度地延长了抗坏血酸自由基的寿命,从对照值20分钟延长至最高80分钟(加入200微克/毫升碧萝芷时)。黄酮类化合物可能是从抗坏血酸盐再生抗坏血酸,或者与抗坏血酸氧化酶相互作用,从而阻止抗坏血酸结合。当将已知的抗坏血酸氧化酶抑制剂对甲酚加入抗坏血酸 - 抗坏血酸氧化酶反应混合物中时,抗坏血酸自由基信号强度显著降低,并且没有显示出黄酮类化合物所观察到的随时间的衰减。这表明黄酮类化合物与抗坏血酸自由基之间发生了直接相互作用。所测试的一些黄酮类化合物,杨梅素、多酚和茶黄素似乎与抗坏血酸竞争抗坏血酸氧化酶,因为它们表现出饱和行为。通过改变实验条件检测到了杨梅素自由基,从而证实了杨梅素与抗坏血酸氧化酶之间的直接相互作用。