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PMID: 7526272 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Anatomy and physiology of glutamate in the CNS.

Neurology ·Vol. 44 ·No. 11 Suppl 8 ·1994-11-00 ·Pages S7-13

Greenamyre JT, Porter RH

Abstract

Glutamate is the predominant excitatory neurotransmitter in the mammalian CNS. The neurotransmitter pool of glutamate is stored in synaptic vesicles and, upon depolarization, is released into the synaptic cleft in a Ca(2+)-dependent fashion. Glutamate is cleared from the synaptic cleft by high-affinity, Na(+)-dependent uptake carriers located in both neurons and glia. Glutamate acts on several distinct families of receptors, each of which has multiple subtypes with distinct pharmacologic and physiologic properties. Under some conditions, glutamate and related compounds act as excitotoxins and might participate in the events leading to neuronal damage and death in a variety of acute and chronic neurologic disorders. The potential for glutamate to become an excitotoxin is highly dependent upon neuronal metabolic status. A great deal of interest in developing selective, well-tolerated glutamate receptor antagonists for the treatment of a variety of neurologic disorders exists.

MeSH Terms
Central Nervous System/metabolism,physiology Glutamic Acid/adverse effects,metabolism,physiology Humans Ion Channels/physiology Nerve Endings/physiology Nervous System Diseases/etiology Neurotoxins/adverse effects Presynaptic Terminals/physiology Receptors, AMPA/metabolism Receptors, Kainic Acid/physiology Receptors, N-Methyl-D-Aspartate/metabolism
Chemicals
Ion Channels Neurotoxins Receptors, AMPA Receptors, Kainic Acid Receptors, N-Methyl-D-Aspartate Glutamic Acid
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Greenamyre J T
Department of Neurology, University of Rochester (New York) Medical Center 14642-8673.
Porter R H
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
1994-11-00
Pages
S7-13
Language
English
Region
United States
NLM ID
0401060
Subset
IM
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