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非竞争性代谢型谷氨酸受体5拮抗剂的最新进展及其潜在治疗应用

Recent advances in non-competitive mGlu5 receptor antagonists and their potential therapeutic applications.

作者信息

Slassi Abdelmalik, Isaac Methvin, Edwards Louise, Minidis Alexander, Wensbo David, Mattsson Jan, Nilsson Karolina, Raboisson Patrick, McLeod Donald, Stormann Thomas M, Hammerland Lance G, Johnson Edwin

机构信息

NPS Pharmaceuticals Inc. 6850 Goreway Drive, Mississauga, ON, Canada, L4V 1V7.

出版信息

Curr Top Med Chem. 2005;5(9):897-911. doi: 10.2174/1568026054750236.

Abstract

Extensive research into the functions of glutamate and glutamate receptors in the central nervous system (CNS) has shown an essential role of metabotropic glutamate (mGlu) receptors in normal brain functions, but also in neurological and psychiatric disorders. The precise functions of these receptors remain undefined, and progress toward understanding their functions has been hampered by the lack of selective ligands with appropriate pharmacokinetic properties. The Group I mGlu receptor, mGlu5, is well positioned to regulate and fine-tune neuronal excitability and synaptic transmission through its modulation of various signal transduction pathways and interactions with other transmitter systems. Therefore, the mGlu5 receptor may be an important therapeutic target for the treatment of disorders of the central nervous system. The discovery of MPEP 3, a non-competitive mGlu5 receptor antagonist, provided a potent, selective, systemically active tool compound for proof of concept studies in animal models of various disease states. These studies have led to greater understanding of possible therapeutic applications of mGlu5 receptor antagonists in recent years, suggesting their use in a number of disease states, including chronic pain, various psychiatric and neurological disorders, substance abuse and withdrawal, obesity and gastroesophageal reflux disease (GERD). Together, these findings have intensified efforts to find other non-competitive mGlu5 receptor antagonists and have led to the discovery of several second-generation compounds, a few of which are in preclinical evaluations. There have been several recent reviews on mGlu receptor. This article highlights recent efforts on the design, synthesis and development of novel, non-competitive mGlu5 receptor antagonists and studies to understand their in vitro mechanisms of action and in vivo pharmacological profiles. Emphasis is also given to recent advances in the potential therapeutic applications of non-competitive mGlu5 receptor antagonists.

摘要

对中枢神经系统(CNS)中谷氨酸和谷氨酸受体功能的广泛研究表明,代谢型谷氨酸(mGlu)受体在正常脑功能以及神经和精神疾病中都起着至关重要的作用。这些受体的确切功能仍不明确,由于缺乏具有适当药代动力学特性的选择性配体,对其功能的理解进展受到阻碍。I组mGlu受体mGlu5能够通过调节各种信号转导途径以及与其他递质系统的相互作用来调节和微调神经元兴奋性及突触传递。因此,mGlu5受体可能是治疗中枢神经系统疾病的重要治疗靶点。非竞争性mGlu5受体拮抗剂MPEP 3的发现,为各种疾病状态动物模型的概念验证研究提供了一种强效、选择性、全身活性的工具化合物。近年来,这些研究使人们对mGlu5受体拮抗剂可能的治疗应用有了更深入的了解,表明它们可用于多种疾病状态,包括慢性疼痛、各种精神和神经疾病、药物滥用和戒断、肥胖症以及胃食管反流病(GERD)。这些发现共同促使人们加大力度寻找其他非竞争性mGlu5受体拮抗剂,并导致发现了几种第二代化合物,其中一些正处于临床前评估阶段。最近有几篇关于mGlu受体的综述。本文重点介绍了新型非竞争性mGlu5受体拮抗剂的设计、合成和开发方面的最新进展,以及旨在了解其体外作用机制和体内药理学特征的研究。同时也强调了非竞争性mGlu5受体拮抗剂潜在治疗应用方面最近取得的进展。

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