Potentiation by K+ of anoxic release of newly synthesized neuronal glutamate

被引:6
作者
Huang, R
Hertz, L
机构
[1] DUKE UNIV, MED CTR, DEPT CELL BIOL, DURHAM, NC 27710 USA
[2] UNIV SASKATCHEWAN, DEPT PHARMACOL, SASKATOON, SK S7N E5E, CANADA
关键词
anoxia; cell death; cytoprotection; cerebellar granule cells; glutamate; potassium; phenylsuccinate;
D O I
10.1097/00001756-199511270-00030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
GLUTAMATE synthesis from [C-14]glutamine release of newly synthesized, labelled glutamate and cell death in primary cultures of the glutamatergic cerebellar granule cell neurones under anoxic conditions were increased by an elevation of the extracellular potassium concentration. Phenylsuccinate, an inhibitor of transmitochondrial transport and hence of glutamate synthesis from glutamine, decreased the potassium-enhanced glutamate synthesis and the release of newly synthesized glutamate and reduced cell death. Since the extracellular concentration of potassium is elevated during brain anoxia and glutamate neurotoxicity is thought to contribute to neuronal cell death under this condition, these observations may be of functional and potentially therapeutic relevance.
引用
收藏
页码:2404 / 2408
页数:5
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