5-HT3 receptor antagonists inhibit sensory neuropeptide release from the rat spinal cord

Neuroreport. 1990 Oct;1(2):104-6. doi: 10.1097/00001756-199010000-00005.

Abstract

5-HT3 receptors may be present on primary afferent neurons containing substance P (SP), neurokinin A (NKA) or calcitonin gene-related peptide (CGRP). We investigated the release of SP-, NKA- and CGRP-immunoreactivities (IR) from rat spinal cord slices. Thirty mM potassium chloride caused an increased outflow of all three peptides, i.e. 140-190% of spontaneous release. This release was slightly enhanced in the presence of 3 x 10(-5) M 5-hydroxytryptamine (5-HT). In contrast, a significant inhibition of potassium-evoked, but not of basal NKA-IR and CGRP-IR release was observed when 10(-7) M BRL 43694 or ICS 205-930, two specific 5-HT3 receptor antagonists, were superfused together with 5-HT. In conclusion, 5-HT may facilitate the evoked release of peptides from central terminals of primary sensory neurons via 5-HT3 receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcitonin Gene-Related Peptide / metabolism
  • Granisetron
  • In Vitro Techniques
  • Indazoles / pharmacology
  • Indoles / pharmacology
  • Neurokinin A / metabolism
  • Neurons, Afferent / drug effects
  • Neurons, Afferent / metabolism*
  • Neuropeptides / metabolism*
  • Potassium / metabolism
  • Rats
  • Rats, Inbred Strains
  • Serotonin Antagonists* / pharmacology
  • Spinal Cord / cytology
  • Spinal Cord / drug effects
  • Spinal Cord / metabolism*
  • Substance P / metabolism
  • Tropisetron

Substances

  • Indazoles
  • Indoles
  • Neuropeptides
  • Serotonin Antagonists
  • Substance P
  • Tropisetron
  • Neurokinin A
  • Calcitonin Gene-Related Peptide
  • Potassium
  • Granisetron