Guidarelli A, De Sanctis R, Cellini B, Fiorani M, Dachà M, Cantoni O
Istituto di Farmacologia e Farmacognosia, Via S. Chiara 27, 61029 Urbino, Italy.
Biochem J. 2001 Jun 1;356(Pt 2):509-13. doi: 10.1042/0264-6021:3560509.
A well-established protocol to increase the intracellular content of ascorbic acid was used to investigate the effects of the vitamin on DNA single-strand breakage and toxicity mediated by authentic peroxynitrite (ONOO(-)) in U937 cells. This protocol involved exposure for 60 min to 100 microM dehydroascorbic acid, which was taken up by the cells and converted into ascorbic acid via a GSH-independent mechanism. At the time of exposure to ONOO(-), which was performed in fresh saline immediately after loading with dehydroascorbic acid, the vitamin present in the cells was all in its reduced form. It was found that, in cells that are otherwise ascorbate-deficient, an increase in their ascorbic acid content does not prevent, but rather enhances, the DNA-damaging and lethal responses mediated by exogenous ONOO(-). These results therefore suggest that acute supplementation of ascorbic acid can be detrimental for individuals with pathologies associated with a decrease in ascorbic acid and in which ONOO(-) is known to promote deleterious effects.
采用一种成熟的增加细胞内抗坏血酸含量的方案,来研究该维生素对U937细胞中由真实过氧亚硝酸盐(ONOO(-))介导的DNA单链断裂和毒性的影响。该方案包括将细胞暴露于100 microM脱氢抗坏血酸60分钟,脱氢抗坏血酸被细胞摄取并通过一种不依赖谷胱甘肽的机制转化为抗坏血酸。在加载脱氢抗坏血酸后立即在新鲜盐水中暴露于ONOO(-)时,细胞中存在的维生素全部处于还原形式。研究发现,在其他方面缺乏抗坏血酸的细胞中,其抗坏血酸含量的增加并不能预防,反而会增强由外源性ONOO(-)介导的DNA损伤和致死反应。因此,这些结果表明,急性补充抗坏血酸可能对患有与抗坏血酸减少相关的疾病且已知ONOO(-)会产生有害作用的个体有害。