代谢性谷氨酸受体亚型5拮抗剂MPEP和MTEP

Paul M. Lea IV, Alan I. Faden
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引用次数: 153

摘要

谷氨酸调节中枢神经系统(CNS)的功能,部分通过cAMP和/或IP3/DAG第二信使相关代谢谷氨酸受体(mGluRs)。mGluR5拮抗剂2-甲基-6-(苯乙基)吡啶(MPEP)已被广泛用于阐明mGluR5潜在的生理和病理生理功能。不幸的是,最近的证据表明MPEP具有显著的非特异性作用,包括抑制NMDA受体。相比之下,较新的mGluR5拮抗剂3-[(2-甲基-1,3-噻唑-4-基)乙基]吡啶(MTEP)的体内和体外表征表明,它对mGluR5的选择性比mGluR1更高,对其他mGluR亚型没有影响,并且脱靶效应比MPEP更少。本文回顾了这两种mGluR5拮抗剂的文献,提示它们在神经退行性疾病、成瘾、焦虑和疼痛管理方面的可能用途。
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Metabotropic Glutamate Receptor Subtype 5 Antagonists MPEP and MTEP

Glutamate regulates the function of central nervous system (CNS), in part, through the cAMP and/or IP3/DAG second messenger-associated metabotropic glutamate receptors (mGluRs). The mGluR5 antagonist 2-methyl-6-(phenylethynyl)-pyridine (MPEP) has been extensively used to elucidate potential physiological and pathophysiological functions of mGluR5. Unfortunately, recent evidence indicates significant non-specific actions of MPEP, including inhibition of NMDA receptors. In contrast, in vivo and in vitro characterization of the newer mGluR5 antagonist 3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine (MTEP) indicates that it is more highly selective for mGluR5 over mGluR1, has no effect on other mGluR subtypes, and has fewer off-target effects than MPEP. This article reviews literature on both of these mGluR5 antagonists, which suggests their possible utility in neurodegeneration, addiction, anxiety and pain management.

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