Thalamic NMDA receptors and nociceptive sensory synaptic transmission

Neurosci Lett. 1990 Mar 14;110(3):297-302. doi: 10.1016/0304-3940(90)90863-5.

Abstract

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-l-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 (CNOX) 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 6-Cyano-7-nitroquinoxaline-2,3-dione
  • Action Potentials / drug effects
  • Animals
  • Hot Temperature*
  • Male
  • Nociceptors / drug effects
  • Nociceptors / physiology*
  • Pain / physiopathology
  • Piperazines / pharmacology
  • Quinoxalines / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Neurotransmitter / drug effects
  • Receptors, Neurotransmitter / physiology*
  • Thalamus / drug effects
  • Thalamus / physiology*

Substances

  • Piperazines
  • Quinoxalines
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Neurotransmitter
  • 6-Cyano-7-nitroquinoxaline-2,3-dione
  • 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid