MODULATION OF MEMORY PROCESSING BY GLUTAMIC-ACID RECEPTOR AGONISTS AND ANTAGONISTS

被引:107
作者
FLOOD, JF
BAKER, ML
DAVIS, JL
机构
[1] VET ADM MED CTR,CTR GERIAT RES EDUC & CLIN,ST LOUIS,MO 63106
[2] ST LOUIS UNIV HOSP,DIV GERIATR MED,ST LOUIS,MO 63104
[3] US OFF NAVAL RES,DIV COGNIT & NEURAL SCI 1142,ARLINGTON,VA 22217
关键词
Aspartic acid; Excitatory amino acid; Glutamic acid; Kainic acid; Memory; Mouse; N-Methyl-d-aspartate; Quisqualic acid; Retention;
D O I
10.1016/0006-8993(90)91543-P
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent hypotheses suggesting a critical role of glutamate receptors in hippocampal long-term potentiation and memory processing suggested a closer examination of this transmitter's effect on memory processing in an in vivo setting. New Pharmacological antagonists allow for a separation and examination of various glutamate receptors and their role in memory processing. Mice were trained on a shock avoidance learning paradigm and injected intracerebroventricularly after training with agonists and antagonists of various classes of glutamate receptors. Retention was tested 1 week after training. N-Methyl-d-aspartate (NMDA) receptor agonists enhanced retention in a dose-dependent manner. The enhancement of retention by the non-NMDA agonist kainic acid and quisqualic acid was dose-dependent. l-Glutamic acid, but not d-glutamic acid, enhanced retention. Both NMDA and non-NMDA receptor antagonists produced dose-dependent impairment of retention for footshock training. Administration of the antagonists 24 h after did not impair memorry retention. © 1990.
引用
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页码:197 / 202
页数:6
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