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Commentary| Volume 72, ISSUE 6, P432-433, September 15, 2012

Nothing Is Written in Stone

  • Marian Joëls
    Correspondence
    Address correspondence to Marian Joëls, Ph.D., Department of Neuroscience and Pharmacology, Division of Neuroscience, Rudolf Magnus Institute, University Medical Center Utrecht, PO Box 85500, 3508GA Utrecht, The Netherlands
    Affiliations
    Department of Neuroscience and Pharmacology, Rudolf Magnus Institute, University Medical Center Utrecht, The Netherlands
    Search for articles by this author
  • E. Ronald de Kloet
    Affiliations
    Department of Medical Pharmacology, Leiden University Medical Center, The Netherlands
    Search for articles by this author
      “Nothing is written in stone,” the late Seymour Levine once said about the amazing plasticity of the developing brain in adaptation to an ever-changing environment (
      • Levine S.
      Developmental determinants of sensitivity and resistance to stress.
      ). These adaptations, in response to environmental input, may cause lasting changes in the function of the evolutionary older brain circuitry, underlying emotion and cognition. As a result, adverse experiences in early life are thought to enhance disease vulnerability. However, recent evidence suggests that early adversity does not inevitably lead to a negative outcome (
      • Champagne D.L.
      • Bagot R.C.
      • vanHasselt F.
      • Ramakers G.
      • Meaney M.J.
      • deKloet E.R.
      • et al.
      Maternal care and hippocampal plasticity: Evidence for experience-dependent structural plasticity, altered synaptic functioning, and differential responsiveness to glucocorticoids and stress.
      ). Rather, depending on genes and environmental context, early experience may program the brain for life to come. In this issue, Bagot et al. (
      • Bagot R.C.
      • Tse Y.C.
      • Nguyen H.B.
      • Wong A.S.
      • Meaney M.J.
      • Wong T.P.
      Maternal care influences hippocampal N-methyl-D-aspartate receptor function and dynamic regulation by corticosterone in adulthood.
      ) describe the crucial role of the N-methyl-D-aspartate (NMDA) receptor in this programming effect.
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