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TRANS-ACPD, A SELECTIVE AGONIST OF THE PHOSPHOINOSITIDE-COUPLED EXCITATORY AMINO-ACID RECEPTOR

被引：354
作者：
PALMER, E
MONAGHAN, DT
COTMAN, CW
机构：
[1] UNIV CALIF IRVINE,DEPT PSYCHOBIOL,IRVINE,CA 92717
[2] UNIV CALIF IRVINE,DIV NEUROSURG,IRVINE,CA 92717
来源：
EUROPEAN JOURNAL OF PHARMACOLOGY | 1989年 / 166卷 / 03期
关键词：
D O I：
10.1016/0014-2999(89)90383-X
中图分类号：
R9 [药学];
学科分类号：
1007 ;
摘要：
引用
收藏
页码：585 / 587
页数：3
相关论文
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HARRIS, EW ;
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[2]   COMPLEX STRUCTURE OF QUISQUALATE-SENSITIVE GLUTAMATE RECEPTORS IN RAT CORTEX [J].
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NIELSEN, M .
NEUROSCIENCE LETTERS, 1985, 54 (01) :27-32
[3]  
LONDON ED, 1979, MOL PHARMACOL, V15, P492
[4]   THE EXCITATORY AMINO-ACID RECEPTORS - THEIR CLASSES, PHARMACOLOGY, AND DISTINCT PROPERTIES IN THE FUNCTION OF THE CENTRAL NERVOUS-SYSTEM [J].
MONAGHAN, DT ;
BRIDGES, RJ ;
COTMAN, CW .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1989, 29 :365-402
[5]   GLUTAMATE RECEPTORS AND PHOSPHOINOSITIDE METABOLISM - STIMULATION VIA QUISQUALATE RECEPTORS IS INHIBITED BY N-METHYL-D-ASPARTATE RECEPTOR ACTIVATION [J].
PALMER, E ;
MONAGHAN, DT ;
COTMAN, CW .
MOLECULAR BRAIN RESEARCH, 1988, 4 (02) :161-165
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