Learning, aging and intrinsic neuronal plasticity

In vitro experiments indicate that intrinsic neuronal excitability, as evidenced by changes in the post-burst afterhyperpolarization (AHP) and spike-frequency accommodation, is altered during learning and normal aging in the brain. Here we review these studies, highlighting two consistent findings:...

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Bibliographic Details
Published inTrends in neurosciences (Regular ed.) Vol. 29; no. 10; pp. 587 - 599
Main Authors Disterhoft, John F., Oh, M. Matthew
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.10.2006
Elsevier Science
Elsevier Sequoia S.A
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ISSN0166-2236
1878-108X
DOI10.1016/j.tins.2006.08.005

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Summary:In vitro experiments indicate that intrinsic neuronal excitability, as evidenced by changes in the post-burst afterhyperpolarization (AHP) and spike-frequency accommodation, is altered during learning and normal aging in the brain. Here we review these studies, highlighting two consistent findings: (i) that AHP and accommodation are reduced in pyramidal neurons from animals that have learned a task; and (ii) that AHP and accommodation are enhanced in pyramidal neurons from aging subjects, a cellular change that might contribute to age-related learning impairments. Findings from in vivo single-neuron recording studies complement the in vitro data. From these consistently reproduced findings, we propose that the intrinsic AHP level might determine the degree of synaptic plasticity and learning. Furthermore, it seems that reductions in the AHP must occur before learning if young and aging subjects are to learn a task successfully.
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ISSN:0166-2236
1878-108X
DOI:10.1016/j.tins.2006.08.005