New perspectives for the development of selective metabotropic glutamate receptor ligands

被引:142
作者
Pin, JP
De Colle, C
Bessis, AS
Acher, F
机构
[1] CNRS, INSERM, Ctr Pharmacol Endocrinol, UPR 9023,Lab Mecanismes Mol Commun Cellulaires, F-34094 Montpellier 5, France
[2] Univ Paris 05, CNRS, URA400, F-75270 Paris, France
[3] Parke Davis & Co, Inst Rech Jouveinal, Dept Biochim, F-94265 Fresnes, France
关键词
metabotropic glutamate receptor ligand; G-protein coupling domain; receptor activation; regulating site; molecular modeling; neuroactive molecule;
D O I
10.1016/S0014-2999(99)00258-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The metabotropic glutamate receptors are GTP-binding-protein (G-protein) coupled receptors that play important roles in regulating the activity of many synapses in the central nervous system. As such, these receptors are involved in a wide number of physiological and pathological processes. Within the last few years, new potent and selective agonists and antagonists as well as radioligands acting on these receptors have been developed. Molecular modeling studies revealed the structural features of the glutamate binding site, and will be useful for the design of more selective and potent ligands. More interestingly, recent data revealed new regulatory sites on the receptor protein, able either to decrease or potentiate the action of the endogenous ligand. No doubt that in the near future a multitude of new tools to modulate the activity of these receptors will be discovered, enabling the identification of the possible therapeutic applications for these new neuroactive molecules. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:277 / 294
页数:18
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