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Publication Detail
ATP receptor-mediated synaptic currents in the central nervous system.
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Journal Article
  • Authors:
    Edwards FA, Gibb AJ, Colquhoun D
  • Publication date:
    10/09/1992
  • Pagination:
    144, 147
  • Journal:
    Nature
  • Volume:
    359
  • Issue:
    6391
  • Status:
    Published
  • Country:
    England
  • Print ISSN:
    0028-0836
  • Language:
    eng
  • Keywords:
    6-Cyano-7-nitroquinoxaline-2,3-dione, Acetylcholine, Adenosine Triphosphate, Animals, Bicuculline, Brain, Chlorocebus aethiops, Evoked Potentials, Somatosensory, Ganglionic Blockers, Glutamates, Glutamic Acid, Hexamethonium, Hexamethonium Compounds, In Vitro Techniques, Ion Channels, Kynurenic Acid, Mecamylamine, Quinoxalines, Receptors, N-Methyl-D-Aspartate, Receptors, Neurotransmitter, Signal Transduction, Suramin, Tetrodotoxin, gamma-Aminobutyric Acid
Abstract
Until now, the only well documented, fast excitatory neurotransmitter in the brain has been glutamate. Although there is evidence for adenosine 5'-triphosphate (ATP) acting as a transmitter in the peripheral nervous system, suggestions for such a role in the central nervous system have so far not been supported by any direct evidence. Here we report the recording of evoked and miniature synaptic currents in the rat medial habenula. The fast rise time of the currents showed that they were mediated by a ligand-activated ion channel rather than a second messenger system, thus limiting the known transmitter candidates. Evidence was found for the presence on the cells of glutamate, gamma-aminobutyric acid, acetylcholine and ATP receptors, but not for 5-hydroxytryptamine (5HT3) or glycine receptors. The evoked currents were unaffected by blockers of glutamate, gamma-aminobutyric acid or acetylcholine receptors but were blocked by the ATP receptor-blocker, suramin and the desensitizing ATP receptor-agonist alpha,beta-methylene-ATP. Our evidence identifies for the first time synaptic currents in the brain, mediated directly by ATP receptors.
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Div of Biosciences
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Neuro, Physiology & Pharmacology
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Neuro, Physiology & Pharmacology
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