GYKI 52466 inhibits AMPA/kainate and peripheral mechanical sensory activity

Dénes Budai, Alice A Larson

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


The selectivity of the 2,3-benzodiazepine compound, GYKI 52466, was tested on wide dynamic range (WDR) dorsal horn neurons of the rat spinal cord. Using extracellular recordings, neurons were characterized by stimulation with noxious and innocuous intensities of the receptive field. In most cells, responses to iontophoretically applied (R, S)-α-amino-3-hydroxy-5-methylisoxa-zole-4-propionate (AMPA) or kainic acid (KA), but not N-metnyl-D-aspartate (NMDA), were profoundly reduced by iontophoretic ejection of GYKI 52466. The inhibition usually lasted for 5-30 min following application of GYKI 52466. In a few neurons, responses to NMDA were also decreased by GYKI 52466. Responses to both noxious and innocuous mechanical stimulation were reduced in the presence of GYKI 52466. The results provide evidence for the selective inhibition by GYKI 52466 of AMPA/KA receptor-mediated functions and support the involvement of these receptors in spinal mechanical nociception.

Original languageEnglish (US)
Pages (from-to)881-884
Number of pages4
Issue number8
StatePublished - Apr 1994


  • AMPA
  • Kainate
  • NMDA
  • Nociception
  • Spinal cord
  • Wide dynamic range neurons


Dive into the research topics of 'GYKI 52466 inhibits AMPA/kainate and peripheral mechanical sensory activity'. Together they form a unique fingerprint.

Cite this