Nutrition and Food Technology Institute, University of Chile, Santiago 7830489, Chile.
Bioinorg Chem Appl. 2011;2011:674149. doi: 10.1155/2011/674149. Epub 2011 Sep 20.
The physiologically occurring copper-glutathione complex, [Cu(I)-GSH], has the ability to react continually with oxygen, generating superoxide anions (O(2) (∙-)). We addressed here the effects that superoxide removal has on the redox state of Cu(I) and GSH present in such complex and assessed the formation of Cu(II)-GSSG as a final oxidation product. In addition, we investigated the potential of a source of O(2) (∙-) external to the Cu(I)-GSH complex to prevent its oxidation. Removal of O(2) (∙-) from a Cu(I)-GSH-containing solution, whether spontaneous or Tempol-induced, led to time-dependent losses in GSH that were greater than those affecting the metal. The losses in GSH were not accompanied by increments in GSSG but were largely accounted for by the cumulative formation of Cu(II)-GSSG molecules. Notably, the redox changes in Cu(I) and GSH were totally prevented when Cu(I)-GSH was coincubated with hypoxanthine/xanthine oxidase. Data suggest that the generation of O(2) (∙-) by Cu(I)-GSH implies the obliged formation of an intermediate whose subsequent oxidation into Cu(II)-GSSG or back reduction into Cu(I)-GSH is favoured by either the removal or the addition of O(2) (∙-), respectively.
生理状态下的铜-谷胱甘肽复合物[Cu(I)-GSH]能够与氧气持续反应,生成超氧阴离子(O(2) (∙-))。我们在此研究了超氧阴离子清除对该复合物中 Cu(I)和 GSH 氧化还原状态的影响,并评估了 Cu(II)-GSSG 作为最终氧化产物的形成情况。此外,我们还研究了 Cu(I)-GSH复合物外部 O(2) (∙-)源对其氧化的抑制潜力。无论自发清除还是 Tempol 诱导清除 O(2) (∙-),都会导致含 Cu(I)-GSH溶液中的 GSH 持续损失,其损失程度大于对金属的影响。GSH 的损失并未伴随着 GSSG 的增加,而是主要归因于 Cu(II)-GSSG 分子的累积形成。值得注意的是,当 Cu(I)-GSH与次黄嘌呤/黄嘌呤氧化酶同时孵育时,Cu(I)和 GSH 的氧化还原变化完全被阻止。数据表明,Cu(I)-GSH生成 O(2) (∙-)意味着必需形成一种中间体,随后其氧化成 Cu(II)-GSSG 或回还原成 Cu(I)-GSH,分别受到 O(2) (∙-)的清除或添加的促进。