mGluR5 antagonists: Discovery, characterization and drug development

被引:0
|
作者
Gasparini, Fabrizio [1 ]
Bilbe, Graeme [1 ]
Gomez-Mancilla, Baltazar [2 ]
Spooren, Will [3 ]
机构
[1] Novartis Pharma AG, Novartis Inst BioMed Res Basel, Neurosci Discovery, CH-4002 Basel, Switzerland
[2] Novartis Pharma AG, Exploratory Dev, CH-4002 Basel, Switzerland
[3] F Hoffmann La Roche & Co Ltd, CH-4070 Basel, Switzerland
关键词
anxiety; depression; fragile X syndrome; gastroesophageal reflux disorder; metabotropic glutamate receptors; MPEP; pain; Parkinson's disease;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Disturbances of glutamate-mediated neurotransmission have been implicated in a broad range of nervous system disorders. Numerous attempts to correct nervous system dysfunction by pharmacological intervention at glutamate receptors have been made, and some of the approaches have achieved a high level of preclinical validation. However, in a number of cases involving agents acting as blockers of the ionotropic glutamate receptors, clinical success could not be achieved, mostly because of the lack of a therapeutic window. The identification of the metabotropic glutamate receptor (mGluR) family and their modulatory role in the control of neurotransmission provided a new means to alter glutamatergic transmission. Furthermore, selective agents acting as allosteric antagonists at the mGluR5 subtype have demonstrated therapeutic potential. The identification and characterization of mGluR5 antagonists and recent progress in clinical development are summarized.
引用
收藏
页码:655 / 665
页数:11
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