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PMID: 9687579 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

ATP receptor-mediated enhancement of fast excitatory neurotransmitter release in the brain.

Molecular pharmacology ·Vol. 54 ·No. 2 ·1998-08-00 ·Pages 372-8

Khakh BS, Henderson G

Abstract

ATP-gated cation channels (P2X receptors) exist on the soma of proprioceptive neurons in the trigeminal mesencephalic nucleus (MNV) in the brain stem. However, these pseudomonopolar neurons seem to receive no synaptic input to their soma; we therefore hypothesized that in MNV neurons, the P2X receptors of importance may be those located on their central terminal projections. Here, we show in trigeminal mesencephalic motor nucleus neurons, which receive their major input from the MNV, that both exogenous ATP (1 mM) and high frequency focal stimulation to evoke endogenous ATP release enhanced the frequency of spontaneous fast excitatory postsynaptic currents (EPSCs) with no change in their amplitude. The enhancement was reduced by the antagonists suramin (300 microM) and pyridoxal-phosphate-6-azophenyl-2',4'-disulfonic acid (30 microM) and persisted when action potential conduction was blocked with tetrodotoxin (1 microM). Thus, functional P2X receptors are expressed on nerve terminals in the brain stem, where they increase the spontaneous release of glutamate onto trigeminal mesencephalic motor nucleus neurons.

MeSH Terms
Adenosine Triphosphate/metabolism Animals Brain/metabolism Electric Stimulation Glutamic Acid/metabolism Neurons/metabolism Rats Receptors, Purinergic P2/metabolism
Chemicals
Receptors, Purinergic P2 Glutamic Acid Adenosine Triphosphate
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Khakh B S
Department of Pharmacology, School of Medical Sciences, University of Bristol, Bristol BS8 1TD, UK. balkhakh@cco.caltech.edu
Henderson G
Article Info
Journal
Molecular pharmacology
Abbr.
Mol Pharmacol
ISSN
0026-895X
Published
1998-08-00
Pages
372-8
Language
English
Region
United States
NLM ID
0035623
Subset
IM
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