Metabotropic glutamate receptors as novel targets for anxiety and stress disorders

被引:497
作者
Swanson, CJ [1 ]
Bures, M [1 ]
Johnson, MP [1 ]
Linden, AM [1 ]
Monn, JA [1 ]
Schoepp, DD [1 ]
机构
[1] Eli Lilly & Co, Div Neurosci, Indianapolis, IN 46285 USA
关键词
D O I
10.1038/nrd1630
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Anxiety and stress disorders are the most commonly occurring of all mental illnesses, and current treatments are less than satisfactory. So, the discovery of novel approaches to treat anxiety disorders remains an important area of neuroscience research. Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system, and G-protein-coupled metabotropic glutamate ( mGlu) receptors function to regulate excitability via pre- and postsynaptic mechanisms. Various mGlu receptor subtypes, including group I (mGlu(1) and mGlu(5)), group II ( mGlu(2) and mGlu(3)), and group III (mGlu(4), mGlu(7) and mGlu(8)) receptors, specifically modulate excitability within crucial brain structures involved in anxiety states. In addition, agonists for group II (mGlu(2/3)) receptors and antagonists for group I ( in particular mGlu(5)) receptors have shown activity in animal and/or human conditions of fear, anxiety or stress. These studies indicate that metabotropic glutamate receptors are interesting new targets to treat anxiety disorders in humans.
引用
收藏
页码:131 / U34
页数:16
相关论文
共 133 条
[1]   Synthesis and pharmacological characterization of aminocyclopentanetricarboxylic acids: New tools to discriminate between metabotropic glutamate receptor subtypes [J].
Acher, FC ;
Tellier, FJ ;
Azerad, R ;
Brabet, IN ;
Fagni, L ;
Pin, JPR .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (19) :3119-3129
[2]  
[Anonymous], DRUG NEWS PERSPECT
[3]   Metabotropic glutamate receptors: electrophysiological properties and role in plasticity [J].
Anwyl, R .
BRAIN RESEARCH REVIEWS, 1999, 29 (01) :83-120
[4]   NEUROPHARMACOLOGY OF A NEW POTENTIAL ANXIOLYTIC COMPOUND, F2692, 1-(3'-TRIFLUOROMETHYL PHENYL) 1, 4-DIHYDRO 3-AMINO 4-OXO 6-METHYL PYRIDAZINE .1. ACUTE AND INVITRO EFFECTS [J].
ASSIE, MB ;
CHOPIN, P ;
STENGER, A ;
PALMIER, C ;
BRILEY, M .
PSYCHOPHARMACOLOGY, 1993, 110 (1-2) :13-18
[5]   Anxioselective Compounds Acting at the GABAA Receptor Benzodiazepine Binding Site [J].
Atack, John R. .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2003, 2 (04) :213-232
[6]  
Awad H, 2000, J NEUROSCI, V20, P7871
[7]   SAR study of a subtype selective allosteric potentiator of metabotropic glutamate 2 receptor, N-(4-phenoxyphenyl) N-(3-pyridinylmethyl)ethanesulfonamide [J].
Barda, DA ;
Wang, ZQ ;
Britton, TC ;
Henry, SS ;
Jagdmann, GE ;
Coleman, DS ;
Johnson, MP ;
Andis, SL ;
Schoepp, DD .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (12) :3099-3102
[8]  
Bear Mark F., 1994, Current Opinion in Neurobiology, V4, P389, DOI 10.1016/0959-4388(94)90101-5
[9]  
BECK CHM, 1995, J NEUROSCI, V15, P709
[10]   COACTIVATION OF METABOTROPIC GLUTAMATE AND N-METHYL-D-ASPARTATE RECEPTORS IS INVOLVED IN MECHANISMS OF LONG-TERM POTENTIATION MAINTENANCE IN RAT HIPPOCAMPAL CA1 NEURONS [J].
BEHNISCH, T ;
REYMANN, KG .
NEUROSCIENCE, 1993, 54 (01) :37-47