Involvement of voltage-gated sodium channel Na(v)1.8 in the regulation of the release and synthesis of substance P in adult mouse dorsal root ganglion neurons

J Pharmacol Sci. 2008 Oct;108(2):190-7. doi: 10.1254/jphs.08163fp. Epub 2008 Oct 9.

Abstract

This study was conducted to determine whether Na(v)1.8 contributes to the release and/or synthesis of substance P (SP) in adult mice dorsal root ganglion (DRG) neurons. The SP released from cultured DRG neurons of Na(v)1.8 knock-out mice exposed to either capsaicin or KCl was significantly lower than that from wild-type (C57BL/6) mice based on a radioimmunoassay. The SP level of L6 DRG in Na(v)1.8 knock-out mice was also lower than that in wild-type mice. After chronic constriction injury (CCI) of the sciatic nerve, the level of SP decreased in the L6 ipsilateral DRG of wild-type but not Na(v)1.8 knock-out mice. The preprotachykinin-A (PPT-A) mRNAs in L4 - 6 DRGs of Na(v)1.8 knock-out mice also fell to half their normally abundant levels of expression. There were significant increases in Na(v)1.8 expression of the L6 contralateral DRG from wild-type mice and in the percentage of neurons expressing neurokinin-1 receptor in the cytosol of L6 DRGs from wild-type or Na(v)1.8 knock-out mice. These findings suggest that Na(v)1.8 is involved in the regulation of the release and synthesis of SP in the DRG neurons of wild-type mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Capsaicin / pharmacology
  • Cells, Cultured
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Fluorescent Antibody Technique
  • Ganglia, Spinal / drug effects
  • Ganglia, Spinal / metabolism*
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • NAV1.8 Voltage-Gated Sodium Channel
  • Neurons / drug effects
  • Neurons / metabolism*
  • Potassium Chloride / pharmacology
  • Protein Precursors / metabolism
  • RNA, Messenger / metabolism
  • Radioimmunoassay
  • Receptors, Neurokinin-1 / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sciatic Neuropathy / metabolism
  • Sodium Channels / deficiency
  • Sodium Channels / genetics
  • Sodium Channels / metabolism*
  • Substance P / metabolism*
  • Tachykinins / metabolism

Substances

  • NAV1.8 Voltage-Gated Sodium Channel
  • Protein Precursors
  • RNA, Messenger
  • Receptors, Neurokinin-1
  • SCN10A protein, human
  • Scn10a protein, mouse
  • Sodium Channels
  • Tachykinins
  • preprotachykinin
  • Substance P
  • Potassium Chloride
  • Capsaicin