Block of sodium currents in rat dorsal root ganglion neurons by diphenhydramine

Brain Res. 2000 Oct 27;881(2):190-8. doi: 10.1016/s0006-8993(00)02860-2.

Abstract

To elucidate the local anesthetic mechanism of diphenhydramine, its effects on tetrodotoxin-sensitive (TTX-S) and tetrodotoxin-resistant (TTX-R) sodium currents in rat dorsal root ganglion (DRG) neurons were examined by the whole-cell voltage clamp method. Diphenhydramine blocked TTX-S and TTX-R sodium currents with K(d) values of 48 and 86 microM, respectively, at a holding potential of -80 mV. It shifted the conductance-voltage curve for TTX-S sodium currents in the depolarizing direction but had little effect on that for TTX-R sodium currents. Diphenhydramine caused a shift of the steady-state inactivation curve for both types of sodium currents in the hyperpolarizing direction. The time-dependent inactivation became faster and the recovery from the inactivation was slowed by diphenhydramine in both types of sodium currents. Diphenhydramine produced a profound use-dependent block when the cells were repeatedly stimulated with high-frequency depolarizing pulses. The use-dependent block was more pronounced in TTX-R sodium currents. The results show that diphenhydramine blocks sodium channels of sensory neurons similarly to local anesthetics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diphenhydramine / pharmacology*
  • Ganglia, Spinal / drug effects*
  • Ganglia, Spinal / physiology
  • Histamine H1 Antagonists / pharmacology*
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Neurons, Afferent / drug effects*
  • Neurons, Afferent / physiology
  • Rats
  • Sodium Channels / drug effects*
  • Sodium Channels / physiology
  • Tetrodotoxin / pharmacology*

Substances

  • Histamine H1 Antagonists
  • Sodium Channels
  • Tetrodotoxin
  • Diphenhydramine