Activity-dependent synaptic plasticity of NMDA receptors
Activity-dependent, bidirectional control of synaptic efficacy is thought to contribute to many forms of experience-dependent plasticity, including learning and memory. Although most excitatory synapses contain both AMPA and N -methyl- d -aspartate receptors (AMPARs and NMDARs), most studies have fo...
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Published in | The Journal of physiology Vol. 588; no. 1; pp. 93 - 99 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
The Physiological Society
01.01.2010
Blackwell Publishing Ltd Wiley Subscription Services, Inc Blackwell Science Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Activity-dependent, bidirectional control of synaptic efficacy is thought to contribute to many forms of experience-dependent
plasticity, including learning and memory. Although most excitatory synapses contain both AMPA and N -methyl- d -aspartate receptors (AMPARs and NMDARs), most studies have focused on the plasticity of synaptic AMPARs, and on the pivotal
role of NMDA receptors for its induction. Here we review evidence that synaptic NMDARs themselves are subject to long-term
activity-dependent changes by mechanisms that may differ from that of synaptic AMPARs. The bidirectional modulation of NMDAR-mediated
synaptic responses is likely to have important functional implications for NMDAR-dependent forms of synaptic plasticity. |
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Bibliography: | This review was presented at a symposium on which took place at the 11th International Congress on Amino Acids, Peptides and Proteins, Vienna, on 3 August 2009. Neurophysiology of inhibitory & excitatory amino acid receptors ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 This review was presented at a symposium on Neurophysiology of inhibitory & excitatory amino acid receptors which took place at the 11th International Congress on Amino Acids, Peptides and Proteins, Vienna, on 3 August 2009. |
ISSN: | 0022-3751 1469-7793 1469-7793 |
DOI: | 10.1113/jphysiol.2009.179382 |