Activation of Endogenous Antioxidant Defenses in Neuronal Cells Prevents Free Radical‐Mediated Damage

• Published in: Journal of neurochemistry 1998-07, Vol.71 (1), p.69-77
• Main Authors: Duffy, Steven, So, Austin, Murphy, Timothy H.
• Format: Article
• Language: English
• Subjects: Animals; Antioxidant inducer; Antioxidants - metabolism; Biochemistry and metabolism; Biological and medical sciences; Central nervous system; Dimethyl Fumarate; Dopamine - toxicity; Free Radicals - metabolism; Fumarates - pharmacology; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Enzymologic - physiology; Glutathione - metabolism; Glutathione pathway; Glutathione Transferase - genetics; Glutathione Transferase - metabolism; Hybridomas; Hydrogen Peroxide - toxicity; Mice; NAD(P)H Dehydrogenase (Quinone) - genetics; NAD(P)H Dehydrogenase (Quinone) - metabolism; Neuroblastoma; Neurons - drug effects; Neurons - enzymology; Neuroprotective Agents - pharmacology; Oxidants - toxicity; Oxidative stress; Oxidative Stress - drug effects; Oxidative Stress - physiology; Radiation-Sensitizing Agents - pharmacology; Rats; Vertebrates: nervous system and sense organs
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1046/j.1471-4159.1998.71010069.x

: Dopamine (DA) is oxidized to the neurotoxic prooxidant species H2O2, OH•, and DA quinones. We tested whether dimethyl fumarate (DMF), an electrophile shown to induce a pleiotropic antioxidant response in nonneuronal cells, could reduce the toxicity of DA metabolites in neural cells. Treatment of the N18‐RE‐105 neuroblastoma‐retina hybridoma cell line with 30–150 µM dopamine led to cell death within 24 h, which increased steeply with dose, decreased with higher plating density, and was blocked by the H2O2‐metabolizing enzyme catalase. Pretreatment with DMF (30 µM, 24 h) significantly attenuated DA and H2O2 toxicity (40–60%) but not that caused by the calcium ionophore ionomycin. DMF treatment also elevated total intracellular GSH and increased activities of the antioxidant enzymes quinone reductase (QR), glutathione S‐transferase (GST), glutathione reductase, and the pentose phosphate enzyme glucose‐6‐phosphate dehydrogenase. To assess the protective efficacy of QR and GST, a stable cell line was constructed in which these enzymes were overexpressed. Cell death in the overexpressing line was not significantly different from that in a cell line expressing normal QR and GST activities, indicating that these two enzymes alone are insufficient for protection against DA toxicity. Although the relative importance of a single antioxidant enzyme such as QR or GST may be small, antioxidant inducers such as DMF may prove valuable as agents that elicit a broad‐spectrum neuroprotective response.