Calcitonin gene-related peptide enhances TTX-resistant sodium currents in cultured dorsal root ganglion neurons from adult rats

Pain. 2005 Aug;116(3):194-204. doi: 10.1016/j.pain.2005.04.002.

Abstract

The neuropeptide calcitonin gene-related peptide (CGRP) binds to a subpopulation of dorsal root ganglion (DRG) neurons, elevates intracellular calcium, and causes inward currents in about 30% of lumbar DRG neurons. Using whole-cell patch clamp recordings, we found in the present study that application of CGRP to isolated and cultured DRG neurons from the adult rat enhances voltage-gated TTX-resistant (TTX-R) Na(+) inward currents in about 30% of small- to medium-sized DRG neurons. During CGRP, peak densities of Na(+) currents increased significantly. CGRP shifted the membrane conductance of the CGRP-responsive cells towards hyperpolarization without changing the slope of the peak conductance curve. The effect of CGRP was blocked by coadministration of CGRP8-37, an antagonist at the CGRP receptor. The effect of CGRP was also blocked after bath application of PKA14-22, a membrane-permeant blocker of protein kinase A, and PKC19-31, a PKC inhibitor, in the recording pipette. These data show pronounced facilitatory effects of CGRP on TTX-R Na(+) currents in DRG neurons which are mediated through CGRP receptors and intracellular pathways involving protein kinases A and C. Thus, in addition to prostaglandins, CGRP is another mediator that affects TTX-R Na(+) currents which are thought to occur mainly in nociceptive DRG neurons.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Action Potentials / radiation effects
  • Anesthetics, Local / pharmacology*
  • Animals
  • Calcitonin Gene-Related Peptide / pharmacology*
  • Cells, Cultured
  • Cyclic AMP-Dependent Protein Kinases / pharmacology
  • Dose-Response Relationship, Radiation
  • Drug Interactions
  • Electric Stimulation / methods
  • Ganglia, Spinal / cytology*
  • Male
  • Neurons / drug effects*
  • Neurons / physiology
  • Patch-Clamp Techniques / methods
  • Peptide Fragments / pharmacology
  • Protein Kinase C / pharmacology
  • Rats
  • Rats, Wistar
  • Sodium Channels / drug effects
  • Tetrodotoxin / pharmacology*
  • Time Factors

Substances

  • Anesthetics, Local
  • Peptide Fragments
  • Sodium Channels
  • protein kinase C (19-31)
  • Tetrodotoxin
  • Cyclic AMP-Dependent Protein Kinases
  • Protein Kinase C
  • Calcitonin Gene-Related Peptide