Activation of the release of dopamine in the carotid body by veratridine. Evidence for the presence of voltage-dependent Na+ channels in type I cells

Neurosci Lett. 1988 Dec 5;94(3):274-8. doi: 10.1016/0304-3940(88)90030-4.

Abstract

Veratridine (50 microM), an agent known to activate voltage-dependent Na+ channels, induced a strong release of [3H]dopamine from the rabbit carotid body in vitro. The effect of veratridine was dependent on the presence of both Na+ and Ca2+ in the extracellular medium and was abolished by 1 microM tetrodotoxin. These results suggest that chemoreceptor type I cells have voltage-dependent Na+ channels, which could be involved in the depolarization of the cell membrane and activation of voltage-dependent Ca2+ channels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / pharmacology
  • Carotid Body / cytology
  • Carotid Body / metabolism*
  • Dopamine / metabolism*
  • Dopamine Antagonists
  • In Vitro Techniques
  • Rabbits
  • Sodium / pharmacology
  • Sodium Channels / drug effects
  • Sodium Channels / metabolism*
  • Sodium Channels / physiology
  • Tetrodotoxin / pharmacology
  • Veratridine / pharmacology*
  • Veratrine / analogs & derivatives*

Substances

  • Dopamine Antagonists
  • Sodium Channels
  • Tetrodotoxin
  • Veratridine
  • Sodium
  • Veratrine
  • Calcium
  • Dopamine