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Identity of endogenous NMDAR glycine site agonist in amygdala is determined by synaptic activity level

Yan Li, Silvia Sacchi, Loredano Pollegioni, Alo C. Basu, Joseph T. Coyle and Vadim Y. Bolshakov ()
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Yan Li: McLean Hospital, Harvard Medical School
Silvia Sacchi: University of Insubria, ‘The Protein Factory’ Research Center for Protein Biotechnologies, Politecnico di Milano and University of Insubria
Loredano Pollegioni: University of Insubria, ‘The Protein Factory’ Research Center for Protein Biotechnologies, Politecnico di Milano and University of Insubria
Alo C. Basu: McLean Hospital, Harvard Medical School
Joseph T. Coyle: McLean Hospital, Harvard Medical School
Vadim Y. Bolshakov: McLean Hospital, Harvard Medical School

Nature Communications, 2013, vol. 4, issue 1, 1-11

Abstract: Abstract Mechanisms of N-methyl-D-aspartate receptor-dependent synaptic plasticity contribute to the acquisition and retention of conditioned fear memory. However, synaptic rules which may determine the extent of N-methyl-D-aspartate receptor activation in the amygdala, a key structure implicated in fear learning, remain unknown. Here we show that the identity of the N-methyl-D-aspartate receptor glycine site agonist at synapses in the lateral nucleus of the amygdala may depend on the level of synaptic activation. Tonic activation of N-methyl-D-aspartate receptors at synapses in the amygdala under low activity conditions is supported by ambient D-serine, whereas glycine may be released from astrocytes in response to afferent impulses. The release of glycine may decode the increases in afferent activity levels into enhanced N-methyl-D-aspartate receptor-mediated synaptic events, serving an essential function in the induction of N-methyl-D-aspartate receptor-dependent long-term potentiation in fear conditioning pathways.

Date: 2013
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2779

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DOI: 10.1038/ncomms2779

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