Inhibition of glial glutamate transporter GLT-1 augments brain edema after transient focal cerebral ischemia in mice

被引:51
作者
Namura, S
Maeno, H
Takami, S
Jiang, XF
Kamichi, S
Wada, K
Nagata, I
机构
[1] Natl Cardiovasc Ctr, Res Inst, Dept Neurosurg, Suita, Osaka 5658565, Japan
[2] Natl Inst Neurosci, Dept Degenerat Neurol Dis, Natl Ctr Neurol & Psychiat, Kodaira, Tokyo 1878502, Japan
关键词
glutamate transporter; glutamate transporter-1; glia; cerebral ischemia; edema; mice;
D O I
10.1016/S0304-3940(02)00193-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Excessively released glutamate is neurotoxic. Glutamate transporters maintain the extracellular level of glutamate by uptake into glia or neurons. We examined the role of GLT-1, a glial glutamate transporter, in brain damage resulting from transient focal ischemia in mice. Heterozygous gene deletion of GLT-1 significantly augmented brain swelling resulting from 1 h of middle cerebral artery occlusion and 24 h reperfusion. In addition, this gene deletion significantly increased brain water contents in ischemic hemisphere at 6 h after reperfusion. Moreover, intraperitoneal injection of dihydrokainate (10 mg/kg), a specific inhibitor of GLT-1, augmented brain swelling. These data suggest that GLT-1 limits brain edema resulting from ischemia. (C) 2002 Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:117 / 120
页数:4
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