Therapeutic Potential for Metabotropic Glutamate Receptor 7 Modulators in Cognitive Disorders.

IF 3.2 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Harrison H Parent, Colleen M Niswender
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引用次数: 0

Abstract

Metabotropic glutamate receptor 7 (mGlu7) is the most highly conserved and abundantly expressed mGlu receptor in the human brain. The presynaptic localization of mGlu7, coupled with its low affinity for its endogenous agonist, glutamate, are features that contribute to the receptor's role in modulating neuronal excitation and inhibition patterns, including long-term potentiation, in various brain regions. These characteristics suggest that mGlu7 modulation may serve as a novel therapeutic strategy in disorders of cognitive dysfunction, including neurodevelopmental disorders that cause impairments in learning, memory, and attention. Primary mutations in the GRM7 gene have recently been identified as novel causes of neurodevelopmental disorders, and these patients exhibit profound intellectual and cognitive disability. Pharmacological tools, such as agonists, antagonists, and allosteric modulators, have been the mainstay for targeting mGlu7 in its endogenous homodimeric form to probe effects of its function and modulation in disease models. However, recent research has identified diversity in dimerization, as well as trans-synaptic interacting proteins, that also play a role in mGlu7 signaling and pharmacological properties. These novel findings represent exciting opportunities in the field of mGlu receptor drug discovery and highlight the importance of further understanding the functions of mGlu7 in complex neurologic conditions at both the molecular and physiologic levels. SIGNIFICANCE STATEMENT: Proper expression and function of mGlu7 is essential for learning, attention, and memory formation at the molecular level within neural circuits. The pharmacological targeting of mGlu7 is undergoing a paradigm shift by incorporating an understanding of receptor interaction with other cis- and trans- acting synaptic proteins, as well as various intracellular signaling pathways. Based upon these new findings, mGlu7's potential as a drug target in the treatment of cognitive disorders and learning impairments is primed for exploration.

代谢型谷氨酸受体 7 (mGlu7) 调节剂在认知障碍中的治疗潜力。
拟代谷氨酸受体 7(mGlu7)是人脑中最保守、表达最丰富的 mGlu 受体。mGlu7 在突触前定位,加上对其内源性激动剂谷氨酸的低亲和力,这些特点都有助于该受体在不同脑区调节神经元兴奋和抑制模式(包括长期电位)的作用。这些特点表明,mGlu7调节可作为一种新型治疗策略,用于治疗认知功能障碍疾病,包括导致学习、记忆和注意力障碍的神经发育性疾病。最近发现,GRM7 基因的原发性突变是神经发育障碍的新病因,这些患者表现出严重的智力和认知障碍。药理学工具,如激动剂、拮抗剂和异位调节剂,一直是以内源性同源形式的 mGlu7 为靶点,在疾病模型中探究其功能和调节作用的主要手段。然而,最近的研究发现了二聚化的多样性以及跨突触相互作用蛋白,它们也在 mGlu7 信号转导和药理特性中发挥作用。这些新发现为 mGlu 受体药物发现领域带来了令人兴奋的机遇,并凸显了在分子和生理水平上进一步了解 mGlu7 在复杂神经系统疾病中的功能的重要性。意义声明 mGlu7的正确表达和功能对于神经回路中分子水平的学习、注意力和记忆形成至关重要。通过了解受体与其他顺式和反式突触蛋白以及各种细胞内信号通路之间的相互作用,mGlu7 的药理靶点正经历着范式转变。基于这些新发现,mGlu7 作为治疗认知障碍和学习障碍的药物靶点的潜力正亟待挖掘。
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来源期刊
Molecular Pharmacology
Molecular Pharmacology 医学-药学
CiteScore
7.20
自引率
2.80%
发文量
50
审稿时长
3-6 weeks
期刊介绍: Molecular Pharmacology publishes findings derived from the application of innovative structural biology, biochemistry, biophysics, physiology, genetics, and molecular biology to basic pharmacological problems that provide mechanistic insights that are broadly important for the fields of pharmacology and toxicology. Relevant topics include: Molecular Signaling / Mechanism of Drug Action Chemical Biology / Drug Discovery Structure of Drug-Receptor Complex Systems Analysis of Drug Action Drug Transport / Metabolism
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