Inhibition by riluzole of electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenopus oocytes

Eur J Pharmacol. 1993 Apr 28;235(2-3):283-9. doi: 10.1016/0014-2999(93)90147-a.


The effects of riluzole, an anticonvulsant and neuroprotective compound, on excitatory amino acid-evoked currents were studied in Xenopus laevis oocytes injected with mRNA from rat whole brain or cortex. Responses to kainic acid were blocked by riluzole (IC50 = 167 microM) as well as by the quinoxalinedione antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX: IC50 = 0.21 microM) and 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo[f]quinoxaline (NBQX: IC50 = 0.043 microM). Riluzole was somewhat more potent at blocking responses to N-methyl-D-aspartic acid (NMDA: IC50 = 18.2 microM); the competitive NMDA receptor antagonist 2-amino-phosphonovaleric acid (2-APV) yielded an IC50 of 6.1 microM in this system. The inhibition by both riluzole and 2-APV was reversible and did not appear to be use dependent, unlike that of the channel blocker MK-801 ([+]-5-methyl-10,11-dihydro-5H-dibenzo-[a,d]cyclohepten-5,10-imine maleate). It was impossible to demonstrate an interaction of riluzole with any of the known ligand recognition sites on either the kainate or the NMDA receptor in radioligand binding studies. These results suggest a direct but non-competitive action of riluzole on ionotropic glutamate receptors.

MeSH terms

  • 2-Amino-5-phosphonovalerate / pharmacology
  • Animals
  • Electrophysiology
  • Female
  • In Vitro Techniques
  • Ion Channels / drug effects*
  • Kainic Acid / antagonists & inhibitors
  • Kainic Acid / pharmacology*
  • Oocytes / drug effects*
  • RNA, Messenger / isolation & purification
  • Radioligand Assay
  • Rats
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Receptors, N-Methyl-D-Aspartate / drug effects*
  • Riluzole
  • Synaptic Transmission / drug effects
  • Thiazoles / pharmacology*
  • Xenopus laevis


  • Ion Channels
  • RNA, Messenger
  • Receptors, N-Methyl-D-Aspartate
  • Thiazoles
  • 2-Amino-5-phosphonovalerate
  • Riluzole
  • Kainic Acid