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Journal ArticleDOI

Molecular diversity of glutamate receptors and implications for brain function.

Shigetada Nakanishi
- 23 Oct 1992 - 
- Vol. 258, Iss: 5082, pp 597-603
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TLDR
The molecular and functional diversity of the glutamate receptors is reviewed and their implications for integrative brain function are discussed.
Abstract
The glutamate receptors mediate excitatory neurotransmission in the brain and are important in memory acquisition, learning, and some neurodegenerative disorders. This receptor family is classified in three groups: the N-methyl-D-aspartate (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA)-kainate, and metabotropic receptors. Recent molecular studies have shown that many receptor subtypes exist in all three groups of the receptors and exhibit heterogeneity in function and expression patterns. This article reviews the molecular and functional diversity of the glutamate receptors and discusses their implications for integrative brain function.

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Citations
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Journal ArticleDOI

Group I metabotropic glutamate antagonist reduces acute neuronal degeneration and behavioral deficits after traumatic brain injury in rats.

TL;DR: Data indicate that injury-induced acute activation of mGluR1 receptors contributes to both the cellular pathology and the behavioral morbidity associated with TBI.
Journal ArticleDOI

Reversal of Cocaine-Induced Behavioral Sensitization and Associated Phosphorylation of the NR2B and GluR1 Subunits of the NMDA and AMPA Receptors

TL;DR: Pergolide/ondansetron treatment consistently reversed both the behavioral sensitization and the associated changes in the NMDA and AMPA receptor subunits.
Journal ArticleDOI

Interactions between N-acetylaspartylglutamate and AMPA, kainate, and NMDA binding sites.

TL;DR: The hypothesis that, relative to glutamate, NAAG functions as a specific, low potency agonist at N‐methyl‐d‐aspartate subclass of ionotropic acidic amino acid receptors, but the peptide is not likely to activate directly the kainate or quisqualate subclasses of excitatory ionotropic receptors under physiologic conditions is supported.
Journal ArticleDOI

Selective blockade of mGlu5 metabotropic glutamate receptors protects rat hepatocytes against hypoxic damage.

TL;DR: 2‐Methyl‐6‐(2‐phenyl‐1‐ethynyl)‐pyridine (MPEP), a novel, noncompetitive, highly selective mGlu5 receptor antagonist, not only abolished the toxic effect of 1S,3R‐ACPD, but, unexpectedly, was protective by itself against anoxic damage.
Journal ArticleDOI

Molecular identification of NMDA glutamate receptors expressed in bone cells.

TL;DR: It is demonstrated for the first time that osteoblasts and osteoclasts express several NR2 subunits, suggesting a molecular diversity of NMDAR channels similar to what was shown for brain.
References
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Journal ArticleDOI

Heteromeric NMDA receptors: Molecular and functional distinction of subtypes

TL;DR: Molecular cloning identified three complementary DNA species of rat brain, encoding NMDA receptor subunits NMDAR2A (NR2A), NR2B, and NR2C, which are 55 to 70% ientical in sequence, and these are structurally related, with less than 20% sequence identity, to other excitatory amino acid receptor sub Units.
Journal ArticleDOI

The Excitatory Amino Acid Receptors: Their Classes, Pharmacology, and Distinct Properties in the Function of the Central Nervous System

TL;DR: 'The following abbreviations have been used in the text'; I3-N-uxalyl-L-a,l3diaminu-prupiunic acid; ACPD, Trans-l-aminu-cydupentyl-I,3-dicarbuxylate; AMPA, a­ aminU-3-hydruxy-5-methyl-isoxazole-4-propionate; AP4, 2-
Journal ArticleDOI

Excitatory amino acid neurotoxicity and neurodegenerative disease

TL;DR: In vivo and in vitro studies of the cytotoxicity of amino acids are reviewed and the contribution of such toxicity to acute and chronic neurodegenerative disorders is summarized.
Journal ArticleDOI

Molecular cloning and characterization of the rat NMDA receptor

TL;DR: A complementary DNA encoding the rat NMDA receptor has been cloned and characterized and it has been found that this protein has a significant sequence similarity to the AMPA/kainate receptors.
Journal ArticleDOI

Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition

TL;DR: In neurons expressing certain KA-AMPA receptor subunits, glutamate may trigger calcium-dependent intracellular events by activating non-NMDA receptors.
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