Mecamylamine is a selective non-competitive antagonist of N-methyl-D-aspartate- and aspartate-induced currents in horizontal cells dissociated from the catfish retina

Neurosci Lett. 1988 Nov 22;94(1-2):93-8. doi: 10.1016/0304-3940(88)90276-5.

Abstract

The nicotinic acetylcholine channel blockers mecamylamine (MECA) and pempidine (PEMP) blocked voltage-clamped isolated catfish retina cone horizontal responses to aspartate (Asp) and N-methyl-D-aspartate (NMDA) but had little effect on currents induced by kainate and quisqualate. Concentration response curves for NMDA and Asp in the presence of MECA suggested that MECA was a non-competitive inhibitor of NMDA and Asp responses. Further, the MECA and PEMP block of NMDA and Asp-induced currents was highly voltage-sensitive. The non-competitive and voltage-sensitive block of NMDA and Asp-induced currents by MECA suggest that MECA (and PEMP) block the NMDA receptor ion channel.

Publication types

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

MeSH terms

  • Animals
  • Aspartic Acid / analogs & derivatives*
  • Aspartic Acid / antagonists & inhibitors*
  • Aspartic Acid / pharmacology
  • Catfishes
  • Electric Conductivity
  • In Vitro Techniques
  • Mecamylamine / pharmacology*
  • Membrane Potentials / drug effects
  • N-Methylaspartate
  • Retina / drug effects
  • Retina / physiology*

Substances

  • Aspartic Acid
  • N-Methylaspartate
  • Mecamylamine