Voltage-gated potassium channels involved in regulation of physiological function in MrgprA3-specific itch neurons

Brain Res. 2016 Apr 1:1636:161-171. doi: 10.1016/j.brainres.2016.02.014. Epub 2016 Feb 10.

Abstract

Itch is described as an unpleasant or irritating skin sensation that elicits the desire or reflex to scratch. MrgprA3, one of members of the Mrgprs family, is specifically expressed in a subpopulation of dorsal root ganglion (DRG) in the peripheral nervous system (PNS). These MrgprA3-expressing DRG neurons have been identified as itch-specific neurons. They can be activated by the compound, chloroquine, which is used as a drug to treat malaria. In the present study, we labeled these itch-specific neurons using the method of molecular genetic markers, and then studied their electrophysiological properties. We also recorded the cutaneous MrgprA3(-) neurons retrogradely labeled by Dil dye (MrgprA3(-)-Dil). We first found that MrgprA3(+) neurons have a lower excitability than MrgprA3(-) neurons (MrgprA3(-)-non-Dil and MrgprA3(-)-Dil). The number of action potential (AP) was reduced more obviously in MrgprA3(+) neurons than that of in MrgprA3(-) neurons. In most cases, MrgprA3(+) neurons only generated single AP; however, in MrgprA3(-) neurons, the same stimulation could induce multiple AP firing due to the greater voltage-gated potassium (Kv) current existence in MrgprA3(+) than in MrgprA3(-) neurons. Thus, Kv current plays an important role in the regulation of excitability in itch-specific neurons.

Keywords: DRG; Itch; Kv current; MrgprA3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / drug effects
  • Action Potentials / genetics*
  • Amino Acids / administration & dosage
  • Animals
  • Biophysical Phenomena / drug effects
  • Biophysical Phenomena / genetics
  • Biophysics
  • Cells, Cultured
  • Electric Stimulation
  • Female
  • Ganglia, Spinal / cytology*
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neurons / drug effects
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Potassium / pharmacology
  • Potassium Channel Blockers / pharmacology
  • Potassium Channels, Voltage-Gated / physiology*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Tetraethylammonium / pharmacology

Substances

  • Amino Acids
  • Luminescent Proteins
  • MrgprA3 protein, mouse
  • Potassium Channel Blockers
  • Potassium Channels, Voltage-Gated
  • Receptors, G-Protein-Coupled
  • dolaisoleucine
  • Tetraethylammonium
  • Potassium