Heterosynaptic long-term potentiation from the anterior cingulate cortex to spinal cord in adult rats

Mol Pain. 2018 Jan-Dec:14:1744806918798406. doi: 10.1177/1744806918798406. Epub 2018 Aug 14.

Abstract

Spinal nociceptive transmission receives biphasic modulation from supraspinal structures. Recent studies demonstrate that the anterior cingulate cortex facilitates spinal excitatory synaptic transmission and nociceptive reflex. However, whether the top-down descending facilitation can cause long-term synaptic changes in spinal cord remains unclear. In the present study, we recorded C-fiber-evoked field potentials in spinal dorsal horn and found that the anterior cingulate cortex stimulation caused enhancement of C-fiber-mediated responses. The enhancement lasted for more than a few hours. Spinal application of N-methyl-D-aspartate (NMDA) receptor antagonist D-AP5 abolished this enhancement, suggesting that the activation of the NMDA receptor is required. Furthermore, spinal application of methysergide, a serotonin receptor antagonist, also blocked the anterior cingulate cortex-induced spinal long-term potentiation. Our results suggest that the anterior cingulate cortex stimulation can produce heterosynaptic form of long-term potentiation at the spinal cord dorsal horn, and this novel form of long-term potentiation may contribute to top-down long-term facilitation in chronic pain conditions.

Keywords: C-fiber-evoked potentials; Long-term potentiation; NMDA receptors; anterior cingulate cortex; serotonin receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gyrus Cinguli / physiology*
  • Long-Term Potentiation / physiology*
  • Male
  • Posterior Horn Cells / physiology
  • Rats, Sprague-Dawley
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Receptors, Serotonin / metabolism
  • Spinal Cord / physiology*
  • Synapses / physiology*

Substances

  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Serotonin

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