1. Academic Validation
  2. Metabotropic glutamate receptor subtype 5 antagonists MPEP and MTEP

Metabotropic glutamate receptor subtype 5 antagonists MPEP and MTEP

  • CNS Drug Rev. 2006 Summer;12(2):149-66. doi: 10.1111/j.1527-3458.2006.00149.x.
Paul M Lea 4th 1 Alan I Faden
Affiliations

Affiliation

  • 1 New Health Sciences Inc., Bethesda, MD, USA.
Abstract

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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