Acid pH augments excitatory action of ATP on a dissociated mammalian sensory neuron

Neuroreport. 1996 Sep 2;7(13):2151-4. doi: 10.1097/00001756-199609020-00018.

Abstract

ATP stimulates nociceptive neurons via an action on ligand-gated ion channels. Since tissue injury and inflammation result in both localized acidosis and release of ATP, we studied the effect of acid pH on ATP-gated ion channels in rat nodose ganglion neurons. Lowering pH dramatically increased membrane depolarization and action potential firing elicited by ATP. ATP-activated current was enhanced by acid pH and suppressed by alkaline pH. A pH of 7.2 produced the half-maximal effect. Acidification increased the apparent affinity of the receptor for ATP, as evidenced by a parallel shift of the ATP concentration-response curve to the left. The observations suggest that the localized acidosis associated with tissue injury may enhance pain perception via an action on ATP-gated ion channels on mammalian sensory neurons.

MeSH terms

  • Action Potentials / drug effects
  • Adenosine Triphosphate / pharmacology*
  • Animals
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Kinetics
  • Male
  • Membrane Potentials / drug effects
  • Neurons, Afferent / drug effects
  • Neurons, Afferent / physiology*
  • Nodose Ganglion / physiology*
  • Patch-Clamp Techniques
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Adenosine Triphosphate