Glutamate-based therapeutic approaches: allosteric modulators of metabotropic glutamate receptors

被引:88
作者
Marino, MJ
Conn, PJ [1 ]
机构
[1] Merck Res Labs, Neurosci Drug Discovery Movement Disorders, West Point, PA 19486 USA
[2] Vanderbilt Univ, Ctr Med, Dept Pharmacol, Nashville, TN 37232 USA
关键词
D O I
10.1016/j.coph.2005.09.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Metabotropic glutamate receptors (mGluRs) have been proposed as novel targets for the treatment of a variety of disorders. Recently, highly selective allosteric modulators of the mGluRs have been developed by several groups. These allosteric compounds provide an unprecedented degree of selectivity for individual mGluRs, allowing for more detailed functional studies on the roles of these receptors. Furthermore, the allosteric approach avoids many of the hurdles associated with the development of direct agonists as drugs, and provides a clear path forward for clinical proof-of-concept studies. Currently, both positive allosteric modulators of mGluR2 and negative allosteric modulators of mGluR5 hold promise as novel anxiolytics, and positive allosteric modulators of mGluR4 appear to be an exciting new target for the treatment of Parkinson's disease.
引用
收藏
页码:98 / 102
页数:5
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