Antagonism of 5-HT3 receptor mediated currents in murine N1E-115 neuroblastoma cells by (+)-tubocurarine

Neurosci Lett. 1990 Mar 2;110(1-2):107-12. doi: 10.1016/0304-3940(90)90796-c.

Abstract

5-HT3 receptor-mediated membrane currents were recorded from voltage-clamped clonal N1E-115 neuroblastoma cells. The inward current response to ionophoretically applied serotonin (5-HT) was reversibly antagonised by the 5-HT3 receptor antagonists GR 38032F and metoclopramide with IC50 values of 0.2 nM and 14 nM, respectively. Low concentrations of (+)-tubocurarine [+)-Tc) also blocked the response to 5-HT (IC50 = 0.8 nM), but other nicotinic cholinoceptor antagonists (gallamine, vecuronium and trimetaphan) were ineffective when applied at a relatively high concentration (1 microM). Blockade by (+)-Tc was neither voltage- nor use-dependent, suggesting that (+)-Tc does not block 5-HT-activated ion channels in N1E-115 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Imidazoles / pharmacology
  • Ion Channels / drug effects
  • Ion Channels / physiology*
  • Membrane Potentials / drug effects
  • Mice
  • Neuroblastoma
  • Neurons / drug effects
  • Neurons / physiology*
  • Ondansetron
  • Receptors, Nicotinic / drug effects
  • Receptors, Serotonin / drug effects
  • Receptors, Serotonin / physiology*
  • Serotonin Antagonists
  • Tubocurarine / pharmacology*

Substances

  • Imidazoles
  • Ion Channels
  • Receptors, Nicotinic
  • Receptors, Serotonin
  • Serotonin Antagonists
  • Ondansetron
  • Tubocurarine