Herman E J, Bubser M, Conn P J, Jones C K
Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Handb Exp Pharmacol. 2012(213):297-365. doi: 10.1007/978-3-642-25758-2_11.
Metabotropic glutamate receptors (mGluRs) represent exciting targets for the development of novel therapeutic agents for schizophrenia. Recent studies indicate that selective activation of specific mGluR subtypes may provide potential benefits for not only the positive symptoms, but also the negative symptoms and cognitive impairments observed in individuals with schizophrenia. Although optimization of traditional orthosteric agonists may still offer a feasible approach for the activation of mGluRs, important progress has been made in the discovery of novel subtype-selective allosteric ligands, including positive allosteric modulators (PAMs) of mGluR2 and mGluR5. These allosteric mGluR ligands have improved properties for clinical development and have served as key preclinical tools for a more in-depth understanding of the potential roles of these different mGluR subtypes for the treatment of schizophrenia.
代谢型谷氨酸受体(mGluRs)是开发新型精神分裂症治疗药物的令人兴奋的靶点。最近的研究表明,选择性激活特定的mGluR亚型不仅可能对精神分裂症患者出现的阳性症状有益,而且对阴性症状和认知障碍也可能有潜在益处。虽然优化传统的正构激动剂可能仍然是激活mGluRs的可行方法,但在发现新型亚型选择性变构配体方面已经取得了重要进展,包括mGluR2和mGluR5的正变构调节剂(PAMs)。这些变构mGluR配体具有更适合临床开发的特性,并已成为更深入了解这些不同mGluR亚型在精神分裂症治疗中潜在作用的关键临床前工具。