Physiological roles and therapeutic potential of metabotropic glutamate receptors

被引:120
作者
Conn, PJ [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Program Translat Neuropharmacol, Nashville, TN 37232 USA
来源
GLUTAMATE AND DISORDERS OF COGNITION AND MOTIVATION | 2003年 / 1003卷
关键词
metabotropic; glutamate receptor; mGluR; mGlu receptor; allosteric potentiator;
D O I
10.1196/annals.1300.002
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Discovery of mGlu receptors has dramatically influenced our understanding of glutamatergic neurotransmission in the central nervous system. This receptor family provides a mechanism by which activation by glutamate can regulate a number of important neuronal and glial functions that are not typically modulated by ligand-gated ion channels. This includes modulation of neuronal excitability, synaptic transmission, and various metabolic functions. Because of the ubiquitous distribution of glutamatergic synapses, discovery of the mGlu receptors immediately raised the likelihood that mGlu receptors would participate in most, if not all, major functions of the CNS. In addition, the wide diversity and heterogeneous distribution of mGlu receptor subtypes could provide an opportunity for development of pharmacological agents that selectively target specific CNS systems to achieve a therapeutic effect. Over the past decade, an increasing number of agonists and antagonists selective for specific mGlu receptor subtypes have been developed. Use of these pharmacological tools along with genetic approaches has led to major advances in our understanding of the roles of mGlu receptors in regulating CNS systems and animal behavior. These studies suggest that drugs active at mGlu receptors may be useful in treatment of a wide variety of neurological and psychiatric disorders.
引用
收藏
页码:12 / 21
页数:10
相关论文
共 26 条
  • [1] Metabotropic glutamate receptors: electrophysiological properties and role in plasticity
    Anwyl, R
    [J]. BRAIN RESEARCH REVIEWS, 1999, 29 (01) : 83 - 120
  • [2] AGONISTS AT METABOTROPIC GLUTAMATE RECEPTORS PRESYNAPTICALLY INHIBIT EPSCS IN NEONATAL RAT HIPPOCAMPUS
    BASKYS, A
    MALENKA, RC
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1991, 444 : 687 - 701
  • [3] POTASSIUM CONDUCTANCES IN HIPPOCAMPAL-NEURONS BLOCKED BY EXCITATORY AMINO-ACID TRANSMITTERS
    CHARPAK, S
    GAHWILER, BH
    DO, KQ
    KNOPFEL, T
    [J]. NATURE, 1990, 347 (6295) : 765 - 767
  • [4] Pharmacology and functions of metabotropic glutamate receptors
    Conn, PJ
    Pin, JP
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1997, 37 : 205 - 237
  • [5] 3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]-pyridine: A potent and highly selective metabotropic glutamate subtype 5 receptor antagonist with anxiolytic activity
    Cosford, NDP
    Tehrani, L
    Roppe, J
    Schweiger, E
    Smith, ND
    Anderson, J
    Bristow, L
    Brodkin, J
    Jiang, XH
    McDonald, I
    Rao, S
    Washburn, M
    Varney, MA
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (02) : 204 - 206
  • [6] CURRY FE, 1988, ENDOTHELIAL CELLS, V1, P3
  • [7] Davies G., 1982, Current Psychological Reviews, V2, P235, DOI [10.1007/BF03186766, DOI 10.1007/BF02684516]
  • [8] EXCITATORY EFFECTS OF ACPD RECEPTOR ACTIVATION IN THE HIPPOCAMPUS ARE MEDIATED BY DIRECT EFFECTS ON PYRAMIDAL CELLS AND BLOCKADE OF SYNAPTIC INHIBITION
    DESAI, MA
    CONN, PJ
    [J]. JOURNAL OF NEUROPHYSIOLOGY, 1991, 66 (01) : 40 - 52
  • [9] SELECTIVE ACTIVATION OF PHOSPHOINOSITIDE HYDROLYSIS BY A RIGID ANALOG OF GLUTAMATE
    DESAI, MA
    CONN, PJ
    [J]. NEUROSCIENCE LETTERS, 1990, 109 (1-2) : 157 - 162
  • [10] THE EFFECTS OF A SERIES OF OMEGA-PHOSPHONIC ALPHA-CARBOXYLIC AMINO-ACIDS ON ELECTRICALLY EVOKED AND EXCITANT AMINO ACID-INDUCED RESPONSES IN ISOLATED SPINAL-CORD PREPARATIONS
    EVANS, RH
    FRANCIS, AA
    JONES, AW
    SMITH, DAS
    WATKINS, JC
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1982, 75 (01) : 65 - 75