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代谢型谷氨酸受体5正向变构调节剂作为精神分裂症潜在治疗方法的近期专利。

Recent patents on positive allosteric modulators of the metabotropic glutamate 5 receptor as a potential treatment for schizophrenia.

作者信息

Kanuma Kosuke, Aoki Takeshi, Shimazaki Youichi

机构信息

Medicinal Chemistry Laboratories, Molecular Function and Pharmacology Laboratories, Taisho Pharmaceutical Co., Ltd., 1-403 Yoshino-cho, Kita-ku, Saitama, Saitama 331-9530, Japan.

出版信息

Recent Pat CNS Drug Discov. 2010 Jan;5(1):23-34. doi: 10.2174/157488910789753512.

Abstract

The glutamate hypothesis of schizophrenia suggests that hypofunction of N-methyl-D-aspartate (NMDA) receptors may be critical for schizophrenic symptoms; therefore, pharmacological approaches that enhance NMDA function may be beneficial for the treatment of schizophrenia. Several lines of evidence indicate that NMDA and metabotropic glutamate (mGlu) 5 receptors are closely associated signaling partners and that a selective mGlu5 receptor agonist might provide a viable approach for increasing NMDA receptor function in the treatment of schizophrenia. The orthosteric binding sites across members of the mGlu receptor subtype for a particular endogenous ligand are often highly conserved, making it difficult to achieve high selectivity for the specific mGlu5 receptor. The advanced currents of drug discovery have developed multiple highly selective allosteric modulators of mGlu5 receptors. In the present review, we provide an update of the recent patents and development of positive allosteric modulators of the mGlu5 receptor and explore their therapeutic potential for schizophrenia.

摘要

精神分裂症的谷氨酸假说表明,N-甲基-D-天冬氨酸(NMDA)受体功能减退可能是精神分裂症症状的关键因素;因此,增强NMDA功能的药理学方法可能对精神分裂症的治疗有益。多项证据表明,NMDA和代谢型谷氨酸(mGlu)5受体是密切相关的信号转导伙伴,选择性mGlu5受体激动剂可能为增加NMDA受体功能以治疗精神分裂症提供一种可行的方法。mGlu受体亚型成员针对特定内源性配体的正构结合位点通常高度保守,因此难以实现对特定mGlu5受体的高选择性。药物研发的进展已开发出多种mGlu5受体的高选择性变构调节剂。在本综述中,我们提供了mGlu5受体正变构调节剂的近期专利和开发情况的最新信息,并探讨了它们治疗精神分裂症的潜力。

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