THALAMIC NMDA RECEPTORS AND NOCICEPTIVE SENSORY SYNAPTIC TRANSMISSION

被引:58
作者
EATON, SA [1 ]
SALT, TE [1 ]
机构
[1] INST OPHTHALMOL,DEPT VISUAL SCI,JUDD ST,LONDON WC1H 9QS,ENGLAND
关键词
3-(±)-2-carboxypiperazin-4-yl)propyl-1-phosphonate; 6-Cyano-7-nitroquinoxaline-2,3-dione; Excitatory amino acid; N-Methyl-d-aspartate receptor; Nociception; Somatosensory system; Synaptic transmission; Thalamus;
D O I
10.1016/0304-3940(90)90863-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The responses of single thalamic neurones to noxious thermal stimulation were recorded in anaesthetized rats. The selective N-methyl-d-aspartate (NMDA) receptor antagonist, 3-((±)-2-carboxypiperazin-4-yl)propyl-1-phosphonate (CPP), antagonised nociceptive responses when ejected iontophoretically with currents which produced selective antagonism at NMDA receptors. In contrast, the non-NMDA excitatory amino acid receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) had little or no effect on nociceptive responses, although it was able to reduce responses to non-nociceptive mechanoreceptor input. These results show that there is substantial NMDA receptor involvement in thalamic nociceptive responses, and that the contribution of CNQX-sensitive non-NMDA receptors to these responses is not extensive. Furthermore, it appears that nociceptive and non-nociceptive input to the thalamus have distinct synaptic pharmacologies. © 1990.
引用
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页码:297 / 302
页数:6
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