Neurobiological insights and novel therapeutic opportunities for CNS disorders from mGlu receptor allosteric and biased modulation

被引:9
|
作者
Hellyer, Shane
Leach, Katie
Gregory, Karen J. [1 ]
机构
[1] Monash Univ, Monash Inst Pharmaceut Sci, Drug Discovery Biol, Parkville, Vic, Australia
基金
英国医学研究理事会;
关键词
METABOTROPIC GLUTAMATE-RECEPTOR; IN-VIVO EFFICACY; PHARMACOLOGICAL CHARACTERIZATION; DISCOVERY; ACTIVATION; REVEALS; AGONIST; MODELS; POTENT; SCHIZOPHRENIA;
D O I
10.1016/j.coph.2016.10.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The metabotropic glutamate (mGlu) receptor family is a potential therapeutic target for multiple central nervous system (CNS) disorders. However, aspects of mGlu receptor signaling and their role in neural pathways remain to be fully elucidated. Novel subtype selective allosteric modulators have revealed new roles for mGlu receptors in brain health and disease, as well as expanding on previously underappreciated aspects of mGlu signaling such as biased agonism and modulation. Recent advances have improved our understanding of mGlu receptor function. Harnessing these new insights to inform drug discovery programs has the potential to lead to the design and discovery of mGlu allosteric modulators that specifically drive glutamatergic activity toward therapeutically beneficial effects and avoid on-target adverse effect liability.
引用
收藏
页码:49 / 55
页数:7
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