| Literature DB >> 11988341 |
Shobu Namura1, Hiroshi Maeno, Shinya Takami, Xiao-Fan Jiang, Sally Kamichi, Keiji Wada, Izumi Nagata.
Abstract
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.Entities:
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Year: 2002 PMID: 11988341 DOI: 10.1016/s0304-3940(02)00193-3
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046