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靶向代谢型谷氨酸受体 4 的药物发现的机遇与挑战。

Opportunities and challenges in drug discovery targeting metabotropic glutamate receptor 4.

机构信息

a Department of Experimental Medicine , University of Perugia , Perugia , Italy.

b Department of Pharmaceutical Sciences , University of Perugia , Perugia , Italy.

出版信息

Expert Opin Drug Discov. 2018 May;13(5):411-423. doi: 10.1080/17460441.2018.1443076. Epub 2018 Feb 28.

Abstract

Until recently, metabotropic glutamate receptor 4 (mGlu4) has not received adequate attention in terms of drug targeting when compared to other members of the same mGlu receptor family, possibly because of the difficulties encountered in developing highly selective, either orthosteric or allosteric, ligands for this receptor. Areas covered: This review gives to discussion to the past and recent advances (between 2012-2017) in targeting the mGlu4 receptor for the treatment of disorders of the central nervous system (CNS) as well as immunological (neuroinflammation) and metabolic diseases (diabetes). Chemical structures, properties, and pharmacological properties discussed herein were retrieved from the scientific literature databases, PubMed and Google Scholar. Expert opinion: The fertile field of mGlu receptor positive allosteric modulators (PAMs) has recently led to the discovery of foliglurax, a highly selective mGlu4 receptor PAM with optimal bioavailability after oral administration and excellent brain distribution. However, further elucidation of the biological properties of the mGlu4 receptor, including expression and its signalling profile in distinct tissues and cells are still awaited in order to establish the mGlu4 receptor as a definite drug target in several CNS and non-CNS diseases.

摘要

直到最近,与其他代谢型谷氨酸受体(mGluR)家族成员相比,代谢型谷氨酸受体 4(mGlu4)在药物靶向方面尚未受到足够重视,这可能是因为开发该受体的高选择性、变构或正构配体存在困难。

涵盖领域

本综述讨论了过去和最近(2012-2017 年)在针对中枢神经系统(CNS)疾病以及免疫(神经炎症)和代谢性疾病(糖尿病)的 mGlu4 受体进行药物靶向治疗方面的进展。本文中讨论的化学结构、性质和药理学性质均从科学文献数据库PubMed 和 Google Scholar 中检索获得。

专家意见

mGlu 受体正变构调节剂(PAMs)领域的研究成果最近促成了 foliglurax 的发现,foliglurax 是一种高度选择性的 mGlu4 受体 PAM,口服后具有最佳生物利用度和良好的脑分布。然而,为了将 mGlu4 受体确立为几种 CNS 和非 CNS 疾病的明确药物靶点,仍需要进一步阐明 mGlu4 受体的生物学特性,包括其在不同组织和细胞中的表达及其信号转导谱。

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