Synaptic commitment: Developmentally regulated reciprocal changes in hippocampal granule cell NMDA and AMPA receptors over the lifespan

Zhiyong Yang, Michael Krause, Geeta Rao, Bruce L. McNaughton, C. A. Barnes

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

Synaptic transmission in hippocampal field CA1 is largely N-methyl-D-aspartate receptor (NMDAR) dependent during the early postnatal period. It becomes increasingly mediated by α-amino-3-hydroxy-5- methylisoxazole-4-proprionate (AMPA) receptors until an adult ratio of AMPA to NMDA receptors is achieved. It is shown here that increases in the AMPA receptor (AMPAR)-mediated field potential response continue over the life span of the F-344 rat at the perforant path- granule cell synapse in the dentate gyrus. In contrast, the NMDAR-dependent component of the response decreases with age between 1 and 27 mo, leading to an increase of AMPA R/NMDAR ratio with age. One possible explanation of this age difference is that the AMPAR/NMDAR ratio can be modified by experience. To test the idea that the changed ratio is caused by the old rats' longer lives, an intensive 10-mo period of enrichment treatment was given to a group of animals, beginning at 3 mo of age. Compared with animals housed in standard cages, the enrichment treatment did not alter the glutamatergic response ratio measured with field potential recording methods. These data provide support for the conclusion that the observed change with age is developmentally regulated rather than experience dependent. Given the role of the NMDAR in synaptic plasticity, these changes suggest a progressive commitment of perforant path synapses to particular weights over the life span. One possible implication of this effect includes preservation of selected memories, ultimately at the expense of a reduced capacity to store new information.

Original languageEnglish (US)
Pages (from-to)2760-2768
Number of pages9
JournalJournal of neurophysiology
Volume99
Issue number6
DOIs
StatePublished - Jun 1 2008

ASJC Scopus subject areas

  • Neuroscience(all)
  • Physiology

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