Neurobiology of Aging
Volume 32, Issue 8 , Pages 1495-1504, August 2011

Reduced serine racemase expression contributes to age-related deficits in hippocampal cognitive function

  • F.R. Turpin

      Affiliations

    • Centre de Psychiatrie et Neurosciences, INSERM, UMR 894, Université Paris Descartes, Faculté de Médecine René Descartes, Paris, F-75014, France
    • INSERM U862, Neurocentre Magendie, Bordeaux, F-33077, France
    • Université de Bordeaux, Bordeaux, F-33077, France
  • ,
  • B. Potier

      Affiliations

    • Centre de Psychiatrie et Neurosciences, INSERM, UMR 894, Université Paris Descartes, Faculté de Médecine René Descartes, Paris, F-75014, France
  • ,
  • J.R. Dulong

      Affiliations

    • INSERM U862, Neurocentre Magendie, Bordeaux, F-33077, France
    • Université de Bordeaux, Bordeaux, F-33077, France
  • ,
  • P.-M. Sinet

      Affiliations

    • Centre de Psychiatrie et Neurosciences, INSERM, UMR 894, Université Paris Descartes, Faculté de Médecine René Descartes, Paris, F-75014, France
  • ,
  • J. Alliot

      Affiliations

    • Laboratoire de Neuroendocrinologie du Vieillissement, Complexe Scientifique des Cézeaux, Université Blaise Pascal, Aubière, F-63177, France
  • ,
  • S.H.R. Oliet

      Affiliations

    • INSERM U862, Neurocentre Magendie, Bordeaux, F-33077, France
    • Université de Bordeaux, Bordeaux, F-33077, France
  • ,
  • P. Dutar

      Affiliations

    • Centre de Psychiatrie et Neurosciences, INSERM, UMR 894, Université Paris Descartes, Faculté de Médecine René Descartes, Paris, F-75014, France
  • ,
  • J. Epelbaum

      Affiliations

    • Centre de Psychiatrie et Neurosciences, INSERM, UMR 894, Université Paris Descartes, Faculté de Médecine René Descartes, Paris, F-75014, France
  • ,
  • J.-P. Mothet

      Affiliations

    • INSERM U862, Neurocentre Magendie, Bordeaux, F-33077, France
    • Université de Bordeaux, Bordeaux, F-33077, France
  • ,
  • J.-M. Billard

      Affiliations

    • Centre de Psychiatrie et Neurosciences, INSERM, UMR 894, Université Paris Descartes, Faculté de Médecine René Descartes, Paris, F-75014, France
    • Corresponding Author InformationCorresponding author at: Centre de Psychiatrie et Neurosciences, U894, Faculté de médecine, Université Paris Descartes, 2 ter rue d’Alésia, 75014, Paris, France. Tel.: +33 1 40 78 86 47; fax: +33 1 45 80 72 93.

Received 15 May 2009; received in revised form 25 August 2009; accepted 6 September 2009. published online 05 October 2009.

Abstract 

To gain insight into the contribution of d-serine to impaired cognitive aging, we compared the metabolic pathway and content of the amino acid as well as d-serine-dependent synaptic transmission and plasticity in the hippocampus of young and old rats of the Wistar and Lou/C/Jall strains. Wistar rats display cognitive impairments with aging that are not found in the latter strain, which is therefore considered a model of healthy aging. Both mRNA and protein levels of serine racemase, the d-serine synthesizing enzyme, were decreased in the hippocampus but not in the cerebral cortex or cerebellum of aged Wistar rats, whereas the expression of d-amino acid oxidase, which degrades the amino acid, was not affected. Consequently, hippocampal levels of endogenous d-serine were significantly lower. In contrast, serine racemase expression and d-serine levels were not altered in the hippocampus of aged Lou/C/Jall rats. Ex vivo electrophysiological recordings in hippocampal slices showed a marked reduction in N-methyl-d-aspartate-receptor (NMDA-R)-mediated synaptic potentials and theta-burst-induced long-term potentiation (LTP) in the CA1 area of aged Wistar rats, which were restored by exogenous d-serine. In contrast, NMDA-R activation, LTP induction and responses to d-serine were not altered in aged Lou/C/Jall rats.

These results further strengthen the notion that the serine racemase-dependent pathway is a prime target of hippocampus-dependent cognitive deficits with aging. Understanding the processes that specifically affect serine racemase during aging could thus provide key insights into the treatment of memory deficits in the elderly.

Abbreviations: aCSF, artificial cerebrospinal fluid, dAAO, d-amino acid oxidase, d-APV, d-2-amino-5-phosphonovalerate, fEPSP, field excitatory postsynaptic potentials, LTP, long-term potentiation, mRNA, messenger RNA, M-MLV, Moloney Murine Leukemia Virus, NBQX, 2,3-dioxo-6-nitro-1,2,3,4-tetrahydrobenzoquinoxaline-7-sulfonamide, NMDA-R, N-methyl-d-aspartate-receptor, PFV, presynaptic fiber volley, ROS, reactive oxygen species

Keywords: d-serine, Memory, Synaptic plasticity, NMDA receptor, Hippocampus

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PII: S0197-4580(09)00304-2

doi:10.1016/j.neurobiolaging.2009.09.001

Neurobiology of Aging
Volume 32, Issue 8 , Pages 1495-1504, August 2011