ABOLITION OF THE NMDA-MEDIATED RESPONSES BY A SPECIFIC GLYCINE ANTAGONIST, 6,7-DICHLOROQUINOXALINE-2,3-DIONE (DCQX)

被引：28

作者：

YONEDA, Y

OGITA, K

机构：

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1989年 / 164卷 / 02期

关键词：

D O I：

10.1016/0006-291X(89)91535-0

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

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页码：841 / 849

页数：9

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[1] 6,7-DINITRO-QUINOXALINE-2,3-DION AND 6-NITRO,7-CYANO-QUINOXALINE-2,3-DION ANTAGONIZE RESPONSES TO NMDA IN THE RAT SPINAL-CORD VIA AN ACTION AT THE STRYCHNINE-INSENSITIVE GLYCINE RECEPTOR
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[7] INDOLE-2-CARBOXYLIC ACID - A COMPETITIVE ANTAGONIST OF POTENTIATION BY GLYCINE AT THE NMDA RECEPTOR
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[J]. SCIENCE, 1989, 243 (4898) : 1611 - 1613
[8] GLYCINE POTENTIATES THE NMDA RESPONSE IN CULTURED MOUSE-BRAIN NEURONS
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[9] 7-CHLOROKYNURENIC ACID IS A SELECTIVE ANTAGONIST AT THE GLYCINE MODULATORY SITE OF THE N-METHYL-D-ASPARTATE RECEPTOR COMPLEX
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[10] A GLYCINE SITE ASSOCIATED WITH N-METHYL-D-ASPARTIC ACID RECEPTORS - CHARACTERIZATION AND IDENTIFICATION OF A NEW CLASS OF ANTAGONISTS
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