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Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1.

Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1. Research Abstract Details 

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  • Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1. Abstract Text:

    ashok kumarAshok Kumar,jeffrey s thinschmidtJeffrey S Thinschmidt,thomas c fosterThomas C Foster,michael a kingMichael A King,ashok kumarAshok Kumar,jeffrey s thinschmidtJeffrey S Thinschmidt,thomas c fosterThomas C Foster,michael a kingMichael A King,

    Altered hippocampal synaptic plasticity may underlie age-related memory impairment. In acute hippocampal slices from aged (22-24 mo) and young adult (1-12 mo) male Brown Norway rats, extracellular excitatory postsynaptic field potentials were recorded in CA1 stratum radiatum evoked by Schaffer collateral stimulation. We used enhanced Ca(2+) to Mg(2+) ratio and paired-pulse stimulation protocol to induce maximum changes in the synaptic plasticity. Six episodes of theta-burst stimulation (TBS) or nine episodes of paired low-frequency stimulation (pLFS) were used to generate asymptotic long-term potentiation (LTP) and long-term depression (LTD), respectively. In addition, long-term depotentiation (LTdeP) or de-depression (LTdeD) from maximal LTP and LTD were examined using two episodes of pLFS or TBS. Multiple episodes of TBS or pLFS produced significant LTP or LTD in aged and young adult rats; this was not different between age groups. Moreover, there was no significant difference in the amount of LTdeP or LTdeD between aged and young adult rats. Our results show no age differences in the asymptotic magnitude of LTP or LTD, rate of synaptic modifications, development rates, reversal, or decay after postconditioning. Thus impairment of the basic synaptic mechanisms responsible for expression of these forms of plasticity is not likely to account for decline in memory function within this age range.

    Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1. Publishing Authors By Initials

    a kumarA Kumar,js thinschmidtJS Thinschmidt,tc fosterTC Foster,ma kingMA King,a kumarA Kumar,js thinschmidtJS Thinschmidt,tc fosterTC Foster,ma kingMA King,

    For similar abstracts research abstracts see: abstracts research

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    Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of neurophysiology

    VOLUME: 98

    Page Numbers: 594-601

    Journal Abbreviation: J. Neurophysiol.

    ISSN: 0022-3077

    DAY: 6

    MONTH: 06

    YEAR: 2007

    Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 375404

    Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1. Keywords Mesh Terms:

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    Grant and Affiliation Information for Aging effects on the limits and stability of long-term synaptic potentiation and depression in rat hippocampal area CA1.

    AFFILIATION: Dept. of Neuroscience, The Evelyn F. and William L. McKnight Brain Institute, University of Florida, College of Medicine, Gainesville, FL 32610, USA. kash@mbi.ufl.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIA

    GRANT: AG-14979

    ACRONYM: AG

    MEDLINETA: J Neurophysiol

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