NBQX IS A SELECTIVE NON-NMDA RECEPTOR ANTAGONIST IN RAT HIPPOCAMPAL SLICE

被引:17
作者
GOLDSTEIN, JM
LITWIN, LC
机构
[1] Department of Pharmacology, ICI Pharmaceuticals Group, ICI Americas Inc., Wilmington, 19897, DE
关键词
NBQX; DNQX; MAGNESIUM ION; NMDA RECEPTOR; GLYCINE; D-SERINE; GLUTAMATE RECEPTORS; HIPPOCAMPUS;
D O I
10.1007/BF03160028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of NBQX and DNQX on synaptic transmission in Tat hippocampal slice were investigated. Both agents produced dose-dependent blockade of field potentials evoked by low frequency stimulation of Schaffer collateral-commissural fibers recorded in medium containing 4 mM Mg2+ (non-NMDA mediated transmission), with half-maximal effects at about 0.15 muM for NBQX and 1.0 muM for DNQX. When the studies were conducted in Mg2+-free medium (predominantly NMDA mediated transmission), 100 muM NBQX failed to block transmission; however, the response could be completely blocked by the addition of 10 muM of the competitive NMDA antagonist CPP. In contrast, 47 muM DNQX completely blocked secondary field potentials recorded in Mg2+-free medium and this effect could be reversed by the addition of 200 muM of the glycine agonist D-serine. Thus, NBQX exhibited selective blockade of non-NMDA mediated synaptic transmission whereas DNQX had effects at both non-NMDA and NMDA receptor sites, the latter effect via an interaction with the glycine site on the NMDA receptor complex.
引用
收藏
页码:145 / 152
页数:8
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