Ueda J, Sudo A, Mori A, Ozawa T
National Institute of Radiological Sciences, Chiba-shi, Japan.
Arch Biochem Biophys. 1994 Nov 15;315(1):185-9. doi: 10.1006/abbi.1994.1488.
The reactivities of copper(II) complexes with cimetidine (Cim) and cyclo(histidylhistidyl) (CyHH), both of which are SOD model compounds, toward active oxygen species such as superoxide (O2-) and hydrogen peroxide (H2O2) were investigated by electron spin resonance-spin trapping and thiobarbituric acid methods. At physiological pH values, low concentrations of Cu(II) complexes (0.025 mM) with Cim and CyHH could scavenge O2-, but high concentrations of these compexes (0.25 mM) yielded hydroxyl radicals (.OH) during dismutation of O2-. These Cu(II) complexes could directly react with H2O2 to yield .OH. From these results, it is indicated that .OH formed during the dismutation of O2- by high concentration of SOD model compounds may be caused by the reaction of H2O2 generated form dismutation of O2- with Cu(II) complexes. Further, DNA single-stranded breakage was observed during the reactions of H2O2 with these Cu(II) complexes.
研究了铜(II)与西咪替丁(Cim)和环(组氨酰组氨酰)(CyHH)形成的配合物(二者均为超氧化物歧化酶模型化合物)对超氧阴离子(O2-)和过氧化氢(H2O2)等活性氧的反应活性,采用电子自旋共振-自旋捕获法和硫代巴比妥酸法进行研究。在生理pH值下,低浓度的铜(II)与Cim和CyHH形成的配合物(0.025 mM)能够清除O2-,但高浓度的这些配合物(0.25 mM)在O2-歧化过程中会产生羟基自由基(·OH)。这些铜(II)配合物可直接与H2O2反应生成·OH。根据这些结果表明,高浓度超氧化物歧化酶模型化合物在O2-歧化过程中形成的·OH可能是由O2-歧化产生的H2O2与铜(II)配合物反应所致。此外,在H2O2与这些铜(II)配合物的反应过程中观察到了DNA单链断裂。