Substance P modulates single-channel properties of neuronal nicotinic acetylcholine receptors

Neuron. 1990 Mar;4(3):393-403. doi: 10.1016/0896-6273(90)90051-g.

Abstract

Substance P (SP) is present in avian sympathetic ganglia and accelerates the decay rate of acetylcholine (ACh)-evoked macroscopic currents in sympathetic neurons. We demonstrate here that SP modulates ACh-elicited single channels in a manner consistent with an enhancement of ACh receptor (AChR) desensitization. Furthermore, since AChR channel function was monitored in cell-attached patches with SP applied to the extra-patch membrane, the peptide must act via a second messenger mechanism. SP specifically decreases the net ACh-activated single-channel current across the patch membrane by decreasing both channel opening frequency and mean open time kinetics. These experiments demonstrate that a peptide can modulate neuronal AChR function by a second messenger mechanism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylcholine / pharmacology
  • Alkaloids / pharmacology
  • Animals
  • Cell Membrane / physiology
  • Cells, Cultured
  • Chick Embryo
  • Electric Conductivity
  • Electrophysiology / methods
  • Evoked Potentials / drug effects
  • Ganglia, Sympathetic / physiology*
  • Ion Channels / drug effects
  • Ion Channels / physiology*
  • Neurons / drug effects
  • Neurons / physiology*
  • Protein Kinase Inhibitors
  • Receptors, Nicotinic / drug effects
  • Receptors, Nicotinic / physiology*
  • Second Messenger Systems
  • Staurosporine
  • Substance P / pharmacology*

Substances

  • Alkaloids
  • Ion Channels
  • Protein Kinase Inhibitors
  • Receptors, Nicotinic
  • Substance P
  • Staurosporine
  • Acetylcholine