• Source: Metabotropic glutamate receptor 1

The glutamate receptor, metabotropic 1, also known as GRM1, is a human gene which encodes the metabotropic glutamate receptor 1 (mGluR1) protein.




Function


L-Glutamate is the major excitatory neurotransmitter in the central nervous system and activates both ionotropic and metabotropic glutamate receptors. Glutamatergic neurotransmission is involved in most aspects of normal brain function and can be perturbed in many neuropathologic conditions. The metabotropic glutamate receptors are a family of G protein-coupled receptors, that have been divided into 3 groups on the basis of sequence homology, putative signal transduction mechanisms, and pharmacologic properties. Group I, which includes GRM1 alongside GRM5, have been shown to activate phospholipase C. Group II includes GRM2 and GRM3 while Group III includes GRM4, GRM6, GRM7 and GRM8. Group II and III receptors are linked to the inhibition of the cyclic AMP cascade but differ in their agonist selectivities. Alternative splice variants of the GRM1 gene have been described but their full-length nature has not been determined.
A possible connection has been suggested between mGluRs and neuromodulators, as mGluR1 antagonists block adrenergic receptor activation in neurons.




Studies with knockout mice


Mice lacking functional glutamate receptor 1 were reported in 1994. By homologous recombination mediated gene targeting those mice became deficient in mGlu receptor 1 protein. The mice did not show any basic anatomical changes in the brain but had impaired cerebellar long-term depression and hippocampal long-term potentiation. In addition they had impaired motor functions, characterized by impaired balance. In the Morris watermaze test, an assay for learning abilities, those mice needed significantly more time to successfully complete the task.




Clinical significance


Mutations in the GRM1 gene may contribute to melanoma susceptibility. Antibodies against mGluR1 receptors cause cerebellar ataxia and impair long-term depression (LTDpathies) in the cerebellum.




Ligands


In addition to the orthosteric site (the site where the endogenous ligand glutamate binds) at least two distinct allosteric binding sites exist on the mGluR1. A respectable number of potent and specific allosteric ligands – predominantly antagonists/inhibitors – has been developed in recent years, although no orthosteric subtype-selective ligands have yet been discovered (2008).

JNJ-16259685: highly potent, selective non-competitive antagonist
R-214,127 and [3H]-analog: high-affinity, selective allosteric inhibitor
YM-202,074: high-affinity, selective allosteric antagonist
YM-230,888: high-affinity, selective allosteric antagonist
YM-298,198 and [3H]-analog: selective non-competitive antagonist
FTIDC: highly potent and selective allosteric antagonist/inverse agonist
A-841,720: potent non-competitive antagonist; minor hmGluR5 binding
VU-71: potentiator
Fluorinated 9H-xanthene-9-carboxylic acid oxazol-2-yl-amides: orally available PAMs
Cyclothiazide: selective non-competitive antagonist of the mGluR1 (also AMPA potentiator and minor mGluR5 potentiator but not antagonist)
Riluzole : selective non-competitive antagonist
Theanine : possible indirect inhibitor




See also


Metabotropic glutamate receptor




References






Further reading



This article incorporates text from the United States National Library of Medicine, which is in the public domain.




External links


"Metabotropic Glutamate Receptors: mGlu1". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. Archived from the original on 2016-03-03. Retrieved 2008-12-05.
Overview of all the structural information available in the PDB for UniProt: Q13255 (Metabotropic glutamate receptor 1) at the PDBe-KB.

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