Medical Journals

Interleukin-1beta but Not Tumor Necrosis Factor-alpha Potentiates Neuronal Damage by Quinolinic Acid: Protection by an Adenosine A2a Receptor Antagonist.

Authors:
  • Stone Trevor W
  • Behan Wilhelmina M H

From: Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow, United Kingdom. t.w.stone@bio.gla.ac.uk

Journal of neuroscience research

  • Publish Date: Apr 2007
  • ISSN: 0360-4012
  • Volume: 85
  • Issue: 5
  • Pages: 1077-85
  • Medium: Print
  • Language: English
  • Citation (JAMA): Stone Trevor W, Behan Wilhelmina M H, et al. Interleukin-1beta but Not Tumor Necrosis Factor-alpha Potentiates Neuronal Damage by Quinolinic Acid: Protection by an Adenosine A2a Receptor Antagonist.. J. Neurosci. Res. Apr 2007;85:1077-85

Abstract

Quinolinic acid is an agonist at glutamate receptors sensitive to N-methyl-D-aspartate (NMDA). It has been implicated in neural dysfunction associated with infections, trauma, and ischemia, although its neurotoxic potency is relatively low. This study was designed to examine the effects of a combination of quinolinic acid and the proinflammatory cytokines interleukin-1beta (IL-1beta) and tumor necrosis factor-alpha (TNF-alpha). Compounds were administered to the hippocampus of anesthetized male rats, animals being allowed to recover for 7 days before histological analysis of the hippocampus for neuronal damage estimated by counting of intact, healthy neurons. A low dose of quinolinic acid or IL-1beta produced no damage by itself, but the two together induced a significant loss of pyramidal neurons in the hippocampus. Higher doses produced almost total loss of pyramidal cells. Intrahippocampal TNF-alpha produced no effect alone but significantly reduced the neuronal loss produced by quinolinic acid. The adenosine A(2A) receptor antagonist ZM241385 reduced neuronal loss produced by the combinations of quinolinic acid and IL-1beta. The results suggest that simultaneous quinolinic acid and IL-1beta, both being induced by cerebral infection or injury, are synergistic in the production of neuronal damage and could together contribute substantially to traumatic, infective, or ischemic cerebral damage. Antagonism of adenosine A(2A) receptors protects neurons against the combination of quinolinic acid and IL-1beta.

Mesh Headings (Keywords): Animals, Brain Injuries, Brain Ischemia, Cytoprotection, Drug Synergism, Hippocampus, Interleukin-1beta, Male, Nerve Degeneration, Neuroprotective Agents, Neurotoxins, Pyramidal Cells, Quinolinic Acid, Rats, Rats, Wistar, Receptor, Adenosine A2A, Triazines, Triazoles, Tumor Necrosis Factor-alpha


Check for Full Text / PubMed Unique Identifier (PMID): 17304576


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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