Molecular Pain (Nov 2005)

Feed-forward inhibition: a novel cellular mechanism for the analgesic effect of substance P

  • Yoshimura Megumu,
  • Ko Shanelle W,
  • Xu Hui,
  • Wu Long-Jun,
  • Zhuo Min

DOI
https://doi.org/10.1186/1744-8069-1-34
Journal volume & issue
Vol. 1, no. 1
p. 34

Abstract

Read online

Abstract Substance P (SP) is a neuropeptide well known for its contribution to pain transmission in the spinal cord, however, less is known about the possible modulatory effects of SP. A new study by Gu and colleagues, published in Molecular Pain (2005, 1:20), describes its potential role in feed-forward inhibition in lamina V of the dorsal horn of the spinal cord. This inhibition seems to function through a direct excitation of GABAergic interneurons by substance P released from primary afferent fibers and has a distinct temporal phase of action from the well-described glutamate-dependent feed-forward inhibition. It is believed that through this inhibition, substance P can balance nociceptive output from the spinal cord.