Metabotropic Glutamate Receptors: Physiology, Pharmacology, and Disease

被引:1390
作者
Niswender, Colleen M. [1 ]
Conn, P. Jeffrey
机构
[1] Vanderbilt Univ, Vanderbilt Program Drug Discovery, Nashville, TN 37212 USA
关键词
G-protein-coupled receptors; neuromodulation; allosterism; synaptic plasticity; POSITIVE ALLOSTERIC MODULATORS; LONG-TERM DEPRESSION; PROTEIN-COUPLED RECEPTORS; MGLUR1 MUTANT MICE; FRAGILE-X-SYNDROME; MESSENGER-RNA EXPRESSION; INVERSE AGONIST ACTIVITY; 2ND INTRACELLULAR LOOP; PARKINSONS-DISEASE; WORKING-MEMORY;
D O I
10.1146/annurev.pharmtox.011008.145533
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The metabotropic glutamate receptors (mGluRs) are family C G-protein-coupled receptors that participate in the modulation of synaptic transmission and neuronal excitability throughout the central nervous system. The mGluRs bind glutamate within a large extracellular domain and transmit signals through the receptor protein to intracellular signaling partners. A great deal of progress has been made in determining the mechanisms by which mGluRs are activated, proteins with which they interact, and orthosteric and allosteric ligands that can modulate receptor activity. The widespread expression of mGluRs makes these receptors particularly attractive drug targets, and recent studies continue to validate the therapeutic utility of mGluR ligands in neurological and psychiatric disorders Such as Alzheimer's disease, Parkinson's disease, anxiety, depression, and schizophrenia.
引用
收藏
页码:295 / 322
页数:28
相关论文
共 198 条
[1]
Amino acid recognition by venus flytrap domains is encoded in an 8-residue motif [J].
Acher, FC ;
Bertrand, HO .
BIOPOLYMERS, 2005, 80 (2-3) :357-366
[2]
REDUCED HIPPOCAMPAL LONG-TERM POTENTIATION AND CONTEXT-SPECIFIC DEFICIT IN ASSOCIATIVE LEARNING IN MGLUR1 MUTANT MICE [J].
AIBA, A ;
CHEN, C ;
HERRUP, K ;
ROSENMUND, C ;
STEVENS, CF ;
TONEGAWA, S .
CELL, 1994, 79 (02) :365-375
[3]
REDUCED HIPPOCAMPAL LONG-TERM POTENTIATION AND CONTEXT-SPECIFIC DEFICIT IN ASSOCIATIVE LEARNING IN MGLUR1 MUTANT MICE [J].
AIBA, A ;
CHEN, C ;
HERRUP, K ;
ROSENMUND, C ;
STEVENS, CF ;
TONEGAWA, S .
CELL, 1994, 79 (02) :365-375
[4]
Metabotropic glutamate receptors as a strategic target for the treatment of epilepsy [J].
Alexander, Georgia M. ;
Godwin, Dwayne W. .
EPILEPSY RESEARCH, 2006, 71 (01) :1-22
[5]
Amalric M, 2008, NEUROPHARMACOLOGY, V55, P585
[6]
A novel class of antagonists for metabotropic glutamate receptors, 7-(hydroxyimino)cyclopropa[b]chromen-1a-carboxylates [J].
Annoura, H ;
Fukunaga, A ;
Uesugi, M ;
Tatsuoka, T ;
Horikawa, Y .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1996, 6 (07) :763-766
[7]
Metabotropic glutamate receptors: electrophysiological properties and role in plasticity [J].
Anwyl, R .
BRAIN RESEARCH REVIEWS, 1999, 29 (01) :83-120
[8]
Group III mGluR regulation of synaptic transmission at the SC-CA1 synapse is developmentally regulated [J].
Ayala, Jennifer E. ;
Niswender, Colleen M. ;
Luo, Qingwel ;
Banko, Jessica L. ;
Conn, P. Jeffrey .
NEUROPHARMACOLOGY, 2008, 54 (05) :804-814
[9]
Pharmacological activation of mGlu4 metabotropic glutamate receptors reduces nigrostriatal degeneration in mice treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine [J].
Battaglia, Giuseppe ;
Busceti, Carla L. ;
Molinaro, Gemma ;
Biagioni, Francesca ;
Traficante, Anna ;
Nicoletti, Ferdinando ;
Bruno, Valeria .
JOURNAL OF NEUROSCIENCE, 2006, 26 (27) :7222-7229
[10]
The mGIuR theory of fragile X mental retardation [J].
Bear, MF ;
Huber, KM ;
Warren, ST .
TRENDS IN NEUROSCIENCES, 2004, 27 (07) :370-377