A specific quisqualate agonist inhibits kainate responses induced in Xenopus oocytes injected with rat brain RNA

Neurosci Lett. 1989 May 8;99(3):333-9. doi: 10.1016/0304-3940(89)90469-2.

Abstract

Electrophysiological recording was used to study non-N-methyl-D-aspartate (NMDA) excitatory amino acid (EAA) receptors after injection of rat brain ribonucleic acid (RNA) in Xenopus laevis oocytes. Quisqualate (QA) induced two types of responses, a smooth one and an oscillatory one. These responses are probably mediated by the ionotropic (QAi, a cationic channel) and the metabotropic (QAp, a newly discovered receptor coupled to phospholipase C) QA receptors respectively. alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) only induced a smooth inward current suggesting that it acts only on QAi. Kainate (KA) also induced a smooth inward current, the maximal KA response being 10-fold higher than the maximal AMPA. AMPA inhibited the KA response in a dose-dependent and competitive manner. Amongst various complex hypotheses the simplest to explain these results would be that KA and AMPA both activate the same receptor-channel complex, AMPA inducing a smaller response than KA.

MeSH terms

  • Animals
  • Brain / metabolism*
  • Convulsants / pharmacology*
  • Female
  • Ibotenic Acid / analogs & derivatives
  • Ibotenic Acid / pharmacology
  • Kainic Acid / pharmacology*
  • Kinetics
  • Oocytes / drug effects
  • Oocytes / physiology*
  • Oxadiazoles / pharmacology*
  • Quisqualic Acid
  • RNA / drug effects*
  • RNA / genetics
  • Rats
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Neurotransmitter / drug effects
  • Receptors, Neurotransmitter / physiology*
  • Xenopus laevis
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid

Substances

  • Convulsants
  • Oxadiazoles
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Neurotransmitter
  • Ibotenic Acid
  • RNA
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
  • Quisqualic Acid
  • Kainic Acid