Effect of an Iron-Chelator on Ascorbate-Induced Cytotoxicity

• Published in: Free radical biology & medicine Vol. 23; no. 2; pp. 260 - 270
• Main Authors: Sakagami, Hiroshi, Satoh, Kazue, Fukuchi, Kunihiko, Gomi, Kunihide, Takeda, Minoru
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 1997
• Subjects: Apoptosis; Apoptosis - drug effects; Ascorbic acid; Ascorbic Acid - pharmacology; Ascorbyl radical; Culture Media; Cytotoxicity; Deferoxamine; Deferoxamine - pharmacology; ESR; Free Radicals - metabolism; HL-60 Cells; Humans; Iron; Oxidation-Reduction; Redox potential; Siderophores - pharmacology; Tumor Cells, Cultured; Ascorbic acid; ESR; Cytotoxicity; Iron; Ascorbyl radical; Redox potential; Apoptosis; Deferoxamine
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/S0891-5849(96)00621-1

We investigated the effect of deferoxamine mesylate (DFO), an iron chelator, to test whether ascorbate-induced cytotoxicity is due to iron-catalyzed oxidation. Exposing human promyelocytic leukemic HL-60 cells to either sodium ascorbate or ascorbic acid for 1 h resulted in the progressive production of apoptotic cells characterized by cell shrinkage, as well as nuclear and internucleosomal DNA fragmentation. The addition of micromolar to millimolar concentrations of DFO during the 1-h exposure did not inhibit, but rather enhanced the ascorbate-induced apoptosis in both regular and serum-free RPMI1640 medium. However, a higher concentration of serum significantly inhibited the ascorbate-induced cytotoxicity. In contrast, the cytotoxic activity of ascorbate against T98G human glioblastoma cells was enhanced or reduced by micromolar and millimolar concentrations of DFO, respectively. Ascorbate significantly increased the oxidation potential in the culture medium, and the pro-oxidant action of ascorbate was further augmented by the presence of the cells. DFO did not significantly affect the ascorbyl radical intensity and only slighly reduced the ascorbate-elevated oxidation potential. These data demonstrated that ascorbate can induce cytotoxicity even in iron-deficient medium. © 1997 Elsevier Science Inc.