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Diverse modes of NMDA receptor positive allosteric modulation: Mechanisms and consequences
- Source :
- Neuropharmacology. 112
- Publication Year :
- 2016
-
Abstract
- NMDA Receptors (NMDARs) play key roles in synaptic physiology and NMDAR hypofunction has been implicated in various neurological conditions. In recent years an increasing number of positive allosteric modulators (PAMs) of NMDARs have been discovered and characterized. These diverse PAM classes vary not only in their binding sites and GluN2 subunit selectivity profiles, but also in the nature of their impacts on channel function. Major differences exist in the degree of slowing of channel deactivation and shifting of apparent agonist affinity between different classes of PAMs. Here we review the diverse modes of potentiation by the currently known classes of NMDAR PAMs and discuss the potential consequences of different types of potentiation in terms of desirable and undesirable effects on brain function.This article is part of the Special Issue entitled ‘Ionotropic glutamate receptors’.
- Subjects :
- 0301 basic medicine
Agonist
medicine.drug_class
Excitatory Amino Acid Agents
Allosteric regulation
Plasma protein binding
Biology
Ligands
Receptors, N-Methyl-D-Aspartate
03 medical and health sciences
Cellular and Molecular Neuroscience
0302 clinical medicine
Allosteric Regulation
medicine
Animals
Humans
GNE-6901
Pharmacology
Neurons
Binding Sites
CIQ
Glutamate receptor
GNE-8324
Brain
SGE201
Long-term potentiation
PYD-106
TCN-201
SGE301
Protein Structure, Tertiary
Protein Subunits
030104 developmental biology
nervous system
Pregnenolone
Synapses
Schizophrenia
NMDA receptor
Spermine
Neuroscience
030217 neurology & neurosurgery
Ionotropic effect
Protein Binding
Subjects
Details
- ISSN :
- 18737064
- Volume :
- 112
- Database :
- OpenAIRE
- Journal :
- Neuropharmacology
- Accession number :
- edsair.doi.dedup.....9074f1b4ed9b675046cb67c08c279829