Hydroxyl radical generation dependent on extracellular ascorbate in rat striatum, as determined by microdialysis

被引:10
|
作者
Hara, Shuichi [1 ]
Mizukami, Hajime [1 ]
Kuriiwa, Fumi [1 ]
Endo, Takahiko [1 ]
机构
[1] Tokyo Med Univ, Dept Forens Med, Shinjuku Ku, Tokyo 1608402, Japan
关键词
Ascorbate; Dehydroascorbate; Hydroxyl radical; Rat striatum; Iron; Microdialysis; FOCAL CEREBRAL-ISCHEMIA; BLOOD-BRAIN-BARRIER; FREELY MOVING RATS; VITAMIN-C; IN-VIVO; DEHYDROASCORBIC ACID; LIPID-PEROXIDATION; GLUTAMATE RELEASE; GLOBAL-ISCHEMIA; PRIMATE MODEL;
D O I
10.1016/j.tox.2008.12.025
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ascorbate (AA), an antioxidant substance known as vitamin C, exists in the brain at a high concentration, although transfer into the brain after systemic administration of AA itself is limited. Intraperitoneal administration of dehydroascorbate (DHA) resulted in a rapid and progressive increase in extracellular AA in rat striatum in a dose-dependent manner. DHA administration increased 2,3- and 2,5-dihydroxybenzoate (2,3- and 2,5-DHBA) formation from salicylate in parallel with the increase in extracellular AA. Intrastriatal administration of active AA oxidase (AAO), but not the inactivated enzyme, completely suppressed the increase in 2,3- and 2,5-DHBA formation after the DHA administration. These findings suggest that extracellular AA might stimulate hydroxyl radical ((center dot)OH) generation in the striatum. This is supported by the observation of dose-dependent (center dot)OH generation upon intrastriatal administration of AA itself. In addition, deferoxamine, an iron chelator, decreased basal 2,3- and 2,5-DHBA formation and strongly, though not completely, suppressed the DHA-induced increase of 2,3- and 2,5-DHBA formation. Therefore, increased extracellular AA might function as a prooxidant and stimulate (center dot)OH generation in cooperation with iron in rat striatum. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
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页码:10 / 16
页数:7
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