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Neurosci Lett ; 324(2): 117-20, 2002 May 17.
Article in English | MEDLINE | ID: mdl-11988341

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.


Subject(s)
Brain Edema/genetics , Brain Edema/metabolism , Brain Ischemia/complications , Excitatory Amino Acid Transporter 2/deficiency , Glutamic Acid/metabolism , Kainic Acid/analogs & derivatives , Neuroglia/metabolism , Reperfusion Injury/complications , Animals , Brain/drug effects , Brain/metabolism , Brain/physiopathology , Brain Edema/physiopathology , Excitatory Amino Acid Transporter 2/antagonists & inhibitors , Excitatory Amino Acid Transporter 2/genetics , Extracellular Space/metabolism , Female , Infarction, Middle Cerebral Artery/complications , Kainic Acid/pharmacology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Neurotoxins/metabolism , Neurotransmitter Uptake Inhibitors/pharmacology , Water-Electrolyte Balance/genetics
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