Cortical death caused by striatal administration of AMPA and interleukin-1 is mediated by activation of cortical NMDA receptors

Research output: Contribution to journalArticlepeer-review

Abstract

Striatal coadministration of interleukin-1β (IL-1β) with α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (S-AMPA) in rats results in widespread cortical cell death not caused by either treatment alone. This cortical damage was unaffected by cortical infusion of the AMPA-receptor antagonist NBQX. Cortical infusion of an NMDA-receptor antagonist D-AP5 significantly inhibited (57%; P <0.05) cortical death, but had no effect on the local striatal death. Thus, cortical neuronal death induced by striatal S-AMPA and human recombinant interleukin-1β (hrIL-1β) is mediated by activation of NMDA receptors in the cortex. The authors propose that IL-1β actions on AMPA-receptor mediated cell death may involve the activation of polysynaptic pathways from the striatum to the cortex.
Original languageEnglish
Pages (from-to)1409-1413
Number of pages4
JournalJournal of Cerebral Blood Flow and Metabolism
Volume20
Issue number10
Publication statusPublished - 2000

Keywords

  • AMPA
  • Cortex
  • Excitotoxicity
  • Interleukin-1
  • Neurodegeneration
  • Striatum

Fingerprint

Dive into the research topics of 'Cortical death caused by striatal administration of AMPA and interleukin-1 is mediated by activation of cortical NMDA receptors'. Together they form a unique fingerprint.

Cite this