Synaptic and Extra-Synaptic NMDA Receptors in the CNS

Chapter
Part of the The Receptors book series (REC, volume 30)

Abstract

The N-methyl d-aspartate receptor (NMDAR) is a ligand-gated ion channel that binds the neurotransmitter glutamate. It was pharmacologically identified and differentiated from other ionotropic amino-acid receptors at excitatory synapses in the late 70s for it is activated by NMDA and not kainate. Due to its large calcium conductance, it is involved in many physiological and pathological phenomena, the most notorious of which is synaptic plasticity, considered to be the molecular substrate of learning and memory. During the 40 years that followed their discovery, and owing to other unique properties such as their magnesium-block that makes them key “coincidence detectors”, NMDARs have been mostly studied at synapses. Yet, NMDARs exhibit a great number of other fundamental features that have remained unknown, underappreciated or challenging to study, and that have only become the focus of intense investigation over the past decade. These properties, such as the co-agonist-gating or the subcellular compartmentalization, greatly contribute to the functional diversity of NMDARs and will be the focus of this chapter as they are greatly relevant in the context of their physiological and pathological impact on the central nervous system.

Keywords

NMDA receptor Glutamate receptor Co-agonist d-Serine Glycine Subcellular localization Extrasynaptic Excitotoxicity Synaptic plasticity Subunit composition d-Aspartate Slow inward currents Tonic current Astrocytes Glia 

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Copyright information

© Springer International Publishing AG 2017

Authors and Affiliations

  1. 1.Department of NeuroscienceTufts University School of MedicineBostonUSA
  2. 2.Neurocentre MagendieInserm U1215 and Université de BordeauxBordeauxFrance

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