ANTINOCICEPTION INDUCED BY 3-((PLUS-OR-MINUS)-2-CARBOXYPIPERAZIN-4-YL)-PROPYL-1-PHOSPHONIC ACID (CPP), AN N-METHYL-D-ASPARTATE (NMDA) COMPETITIVE ANTAGONIST, PLUS 6,7-DINITROQUINOXALINE-2,3-DIONE (DNQX), A NON-NMDA ANTAGONIST, DIFFERS FROM THAT INDUCED BY MK-801 PLUS DNQX

被引:11
作者
GOETTL, VM [1 ]
LARSON, AA [1 ]
机构
[1] UNIV MINNESOTA,DEPT VET PATHOBIOL,GRAD PROGRAM NEUROSCI,ST PAUL,MN 55108
关键词
N-METHYL-D-ASPARTATE; NON-N-METHYL-D-ASPARTATE; FORMALIN; PAIN; PCP; 6,7-DINITROQUINOXALINE-2,3-DIONE; 3-((PLUS-OR-MINUS)-2-CARBOXYPIPERAZIN-4-YL)-PROPYL-1-PHOSPHONIC ACID; MK-801;
D O I
10.1016/0006-8993(94)90939-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Excitatory amino acid receptors have been implicated in mediating pain. 3-((+/-)-2-Carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP), a competitive N-methyl-D-aspartate (NMDA) antagonist and MK-801, a phencyclidine (PCP) ligand and non-competitive NMDA antagonist, were injected intrathecally in mice alone or in combination with 6,7-dinitroquinoxaline-2,3-dione (DNQX), a non-NMDA antagonist. When tested in the formalin model of pain, antinociception following CPP plus DNQX was greater than that after MK-801 plus DNQX in both the acute and tonic phases. These dissimilarities are not consistent with activity of CPP and MK-801 at the same sites in the spinal cord.
引用
收藏
页码:334 / 338
页数:5
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