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Overexpression of Cu,Zn Superoxide Dismutase Attenuates Oxidative Inhibition of Astrocyte Glutamate Uptake
Author(s) -
Chen Yongmei,
Ying Weihai,
Simma Vannita,
Chen Yiren,
Copin JeanChristophe,
Chan Pak H.,
Swanson Raymond A.
Publication year - 2000
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2000.0750939.x
Subject(s) - astrocyte , sod1 , superoxide dismutase , glutamate receptor , hypoxanthine , xanthine oxidase , superoxide , reactive oxygen species , biochemistry , neurotoxicity , chemistry , xanthine , excitotoxicity , biology , oxidative stress , pharmacology , endocrinology , central nervous system , toxicity , enzyme , receptor , organic chemistry
Glutamate neurotoxicity in brain is normally prevented by rapid uptake of glutamate by astrocytes. Increased expression of Cu,Zn superoxide dismutase (SOD1) can increase resistance to cerebral ischemia and other oxidative insults, but the cellular mechanisms by which this occurs are not well established. Here we examine whether increased SOD1 expression can attenuate inhibition of astrocyte glutamate uptake by reactive oxygen species. Primary cortical astrocyte cultures were prepared from transgenic mice that overexpress human SOD1 and from nontransgenic littermate controls. Glutamate uptake was assessed after exposure of these cultures to xanthine oxidase plus hypoxanthine, an extracellular superoxide generating system, or to menadione, which generates superoxide in the cytosol. These treatments produced dose‐dependent reductions in astrocyte glutamate uptake, and the reductions were significantly attenuated in the SOD1 transgenic astrocytes. A specific effect of reactive oxygen species on glutamate transporters was suggested by the much smaller inhibitory effects of xanthine oxidase/hypoxanthine and menadione on GABA uptake than on glutamate uptake. These findings suggest that the cerebroprotective effects of increased SOD1 expression during cerebral ischemia‐reperfusion could be mediated in part by astrocyte glutamate transport.