Calcium inhibits willardiine-induced responses in kainate receptor GluR6(Q)/KA-2

Neuroreport. 2001 Jan 22;12(1):163-7. doi: 10.1097/00001756-200101220-00040.

Abstract

A number of studies have demonstrated that willardiine [(S)-1-(2-amino-2-carboxyethyl) pyrimidine-2,4-dione] is a useful agonist for the activation of AMPA/kainate receptors. Here we examine the effect of extracellular calcium on currents evoked by willardiine in HEK 293 cells expressing the GluR6(Q)/KA-2 kainate receptor subunits. At a concentration of 1.8 mM, Ca2+ inhibited the currents induced by 100 microM willardiine by approximately 50%. When extracellular Na+ ions were replaced with Ca2+ ions there were no measurable inward currents. We conclude that Ca2+ inhibition of the willardiine-induced response is concentration dependent.

MeSH terms

  • Alanine / analogs & derivatives
  • Alanine / pharmacology*
  • Calcium Chloride / pharmacology*
  • Cells, Cultured / drug effects
  • GluK2 Kainate Receptor
  • Humans
  • Kidney
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Pyrimidinones
  • Receptors, Kainic Acid / drug effects*
  • Receptors, Kainic Acid / physiology
  • Uracil

Substances

  • Pyrimidinones
  • Receptors, Kainic Acid
  • willardiine
  • Uracil
  • Calcium Chloride
  • Alanine