role of oxidative stress in Sudan IV-induced DNA damage in human liver-derived HepG2 cells

• Published in: Environmental toxicology 2011-06, Vol.26 (3), p.292-299
• Main Authors: Zhang, Yue, An, Yu, Jiang, Liping, Geng, Chengyan, Cao, Jun, Jiang, Lijie, Zhong, Laifu
• Format: Article
• Language: English
• Subjects: 8-Hydroxydeoxyguanosine; 8-OHdG; Animal, plant and microbial ecology; Applied ecology; Azo Compounds - toxicity; Biological and medical sciences; Cell Survival - drug effects; chromosomes; Coloring Agents - toxicity; Comet Assay; Cytotoxins - toxicity; Deoxyguanosine - analogs & derivatives; Deoxyguanosine - metabolism; DNA; DNA Damage; Dose-Response Relationship, Drug; Ecotoxicology, biological effects of pollution; Fundamental and applied biological sciences. Psychology; gel electrophoresis; General aspects; glutathione; Glutathione - metabolism; GSH; Hep G2 Cells; HepG2 cells; Humans; Liver - drug effects; Liver - metabolism; Micronucleus Tests; Oxidation-Reduction; oxidative stress; Oxidative Stress - drug effects; reactive oxygen species; Reactive Oxygen Species - metabolism; SCGE assay; Sudan dyes; Sudan IV; toxicity
• ISSN: 1520-4081; 1522-7278; 1522-7278
• DOI: 10.1002/tox.20558

Objectives: We evaluated the role of oxidative stress in Sudan IV-induced DNA damage, using human liver-derived HepG2 cells. Methods: The DNA damaging effects of Sudan IV in HepG2 cells were evaluated by alkaline single cell gel electrophoresis assay and micronucleus test (MNT). To clarify the underlying mechanisms, we monitored the intracellular generation of reactive oxygen species (ROS) by 2, 7-dichlorofluorescein diacetate assay and the level of oxidative DNA damage by immunoperoxidase staining for 8-hydroxydeoxyguanosine (8-OHdG). Furthermore, the intracellular glutathione (GSH) level was moderated by pretreatment with buthionine-(S,R)-sulfoximine (BSO), a specific GSH synthesis inhibitor. Results: A significant dose-dependent increment in DNA migration was detected at all tested concentrations (25-100 μM) of Sudan IV. And in the MNT, a significant increase of the frequency of micronuclei was found at higher tested concentrations (50-100 μM). The data suggested that Sudan IV caused DNA strand breaks and chromosome breaks. In addition, significantly increased levels of ROS, 8-OHdG formation were observed in HepG2 cells. It was also found that depletion of GSH in HepG2 cells with BSO dramatically increased the susceptibility of HepG2 cells to Sudan IV-induced DNA damage. Conclusions: Based on these data we believe that Sudan IV exerts toxic effects in HepG2 cells, probably through oxidative DNA damage induced by intracellular ROS and depletion of GSH.