Ueda J, Ikota N, Hanaki A, Ozawa T
National Institute of Radiological Sciences, Chiba-shi, Japan.
Biochem Mol Biol Int. 1994 Aug;33(6):1041-8.
The reactivities of new synthetic oligopeptides containing cysteine or histidine towards active oxygen species such as superoxide (O2-) and hydroxyl radical (.OH) were investigated by an electron spin resonance (ESR)-spin trapping method. At physiological pH values, these oligopeptides greatly suppressed the generation of .OH from the reaction of Cu(en)2 (en: ethylenediamine) with hydrogen peroxide (H2O2), although these oligopeptides did not scavenge O2-. The antioxidant mechanism of these oligopeptides is discussed.
采用电子自旋共振(ESR)自旋捕集法研究了含半胱氨酸或组氨酸的新型合成寡肽对超氧阴离子(O2-)和羟基自由基(·OH)等活性氧的反应活性。在生理pH值下,这些寡肽极大地抑制了Cu(en)2(en:乙二胺)与过氧化氢(H2O2)反应生成·OH,尽管这些寡肽不能清除O2-。并对这些寡肽的抗氧化机制进行了讨论。