Neuroprotective actions of novel and potent ligands of group I and group II metabotropic glutamate receptors

被引:46
作者
Kingston, AE
O'Neill, MJ
Bond, A
Bruno, V
Battaglia, G
Nicoletti, F
Harris, JR
Clark, BP
Monn, JA
Lodge, D
Schoepp, DD
机构
[1] Eli Lilly & Co Ltd, Windlesham GU20 6PH, Surrey, England
[2] IMN Neuromed, Pozzilli, Italy
[3] Eli Lilly & Co, Indianapolis, IN USA
来源
NEUROPROTECTIVE AGENTS: FOURTH INTERNATIONAL CONFERENCE | 1999年 / 890卷
关键词
D O I
10.1111/j.1749-6632.1999.tb08022.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The role of group I metabotropic glutamate (mGlu) receptors in neurodegeneration is controversial because of the contradictory effects of mGlu1/5 agonists in in vitro models of neuronal cell death. In this study, novel and selective antagonists of mGlu1 and mGlu5: LY367385 and LY367366 were found to show consistent neuroprotective effects against N-methyl-D-aspartate (NMDA)-induced excitotoxicity in vitro and in vivo. Furthermore, intraventricular administration of LY367385 reduced hippocampal cell death in gerbils subjected to transient global ischemia, Previous studies have also shown that activation of group II mGlu receptors may contribute to neuroprotective mechanisms in vitro and in vivo. Three potent group II mGlu agonists-LY354740, LY379268 and LY389775-were found to attenuate both NMDA excitotoxicity and staurosporine-induced neuronal cell death. LY354740 and LY379268 were protective against transient global Ischemia in gerbils when dosed Intraperitoneally. These results support the view that antagonists of mGlu1 and mGlu5 and agonists of group II mGlu receptors may be useful agents in the therapeutic treatment of neurodegenerative disease.
引用
收藏
页码:438 / 449
页数:12
相关论文
共 31 条
[1]   In vivo inhibition of veratridine-evoked release of striatal excitatory amino acids by the group II metabotropic glutamate receptor agonist LY354740 in rats [J].
Battaglia, G ;
Monn, JA ;
Schoepp, DD .
NEUROSCIENCE LETTERS, 1997, 229 (03) :161-164
[2]   Selective activation of group-II metabotropic glutamate receptors is protective against excitotoxic neuronal death [J].
Battaglia, G ;
Bruno, V ;
Ngomba, RT ;
Di Grezia, R ;
Copani, A ;
Nicoletti, F .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 356 (2-3) :271-274
[3]   LY379268, a potent and selective Group II metabotropic glutamate receptor agonist, is neuroprotective in gerbil global, but not focal, cerebral ischaemia [J].
Bond, A ;
Ragumoorthy, N ;
Monn, JA ;
Hicks, CA ;
Ward, MA ;
Lodge, D ;
O'Neill, MJ .
NEUROSCIENCE LETTERS, 1999, 273 (03) :191-194
[4]   Neuroprotective effects of a systemically active Group II metabotropic glutamate receptor agonist LY354740 in a gerbil model of global ischaemia [J].
Bond, A ;
O'Neill, MJ ;
Hicks, CA ;
Monn, JA ;
Lodge, D .
NEUROREPORT, 1998, 9 (06) :1191-1193
[5]   Neuroprotective activity of the potent and selective mGlula metabotropic glutamate receptor antagonist, (+)-2-methyl-4 caroxyphenylglycine (LY367385): comparison with LY357366, a broader spectrum antagonist with equal affinity for mGlula and mGlu5 receptors [J].
Bruno, V ;
Battaglia, G ;
Kingston, A ;
O'Neill, MJ ;
Catania, MV ;
Di Grezia, R ;
Nicoletti, F .
NEUROPHARMACOLOGY, 1999, 38 (02) :199-207
[6]   ACTIVATION OF METABOTROPIC GLUTAMATE RECEPTORS COUPLED TO INOSITOL PHOSPHOLIPID HYDROLYSIS AMPLIFIES NMDA-INDUCED NEURONAL DEGENERATION IN CULTURED CORTICAL-CELLS [J].
BRUNO, V ;
COPANI, A ;
KNOPFEL, T ;
KUHN, R ;
CASABONA, G ;
DELLALBANI, P ;
CONDORELLI, DF ;
NICOLETTI, F .
NEUROPHARMACOLOGY, 1995, 34 (08) :1089-1098
[7]   PROTECTIVE EFFECT OF THE METABOTROPIC GLUTAMATE-RECEPTOR AGONIST, DCG-IV, AGAINST EXCITOTOXIC NEURONAL DEATH [J].
BRUNO, V ;
COPANI, A ;
BATTAGLIA, G ;
RAFFAELE, R ;
SHINOZAKI, H ;
NICOLETTI, F .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 256 (01) :109-112
[8]  
Bruno V, 1998, J NEUROSCI, V18, P9594
[9]   DCG-IV selectively attenuates rapidly triggered NMDA-induced neurotoxicity in cortical neurons [J].
Buisson, A ;
Yu, SP ;
Choi, DW .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1996, 8 (01) :138-143
[10]   THE INHIBITORY MGLUR AGONIST, S-4-CARBOXY-3-HYDROXY-PHENYLGLYCINE SELECTIVELY ATTENUATES NMDA NEUROTOXICITY AND OXYGEN GLUCOSE DEPRIVATION-INDUCED NEURONAL DEATH [J].
BUISSON, A ;
CHOI, DW .
NEUROPHARMACOLOGY, 1995, 34 (08) :1081-1087