European Neuropsychopharmacology
Volume 21, Issue 1 , Pages 45-62, January 2011

Effect of chronic mild stress on hippocampal transcriptome in mice selected for high and low stress-induced analgesia and displaying different emotional behaviors

  • Pawel Lisowski

      Affiliations

    • Department of Molecular Biology, Institute of Genetics and Animal Breeding, Polish Academy of Sciences, Jastrzebiec, Poland
  • ,
  • Grzegorz R. Juszczak

      Affiliations

    • Department of Animal Behavior, Institute of Genetics and Animal Breeding, Polish Academy of Sciences, Jastrzebiec, Poland
  • ,
  • Joanna Goscik

      Affiliations

    • Department of Software Engineering, Bialystok Technical University, Bialystok, Poland
  • ,
  • Marek Wieczorek

      Affiliations

    • Department of Neurophysiology, University of Lodz, Lodz, Poland
  • ,
  • Lech Zwierzchowski

      Affiliations

    • Department of Molecular Biology, Institute of Genetics and Animal Breeding, Polish Academy of Sciences, Jastrzebiec, Poland
  • ,
  • Artur H. Swiergiel

      Affiliations

    • Department of Animal Behavior, Institute of Genetics and Animal Breeding, Polish Academy of Sciences, Jastrzebiec, Poland
    • Department of Animal Physiology, Institute of Biology, Gdansk University, Gdansk, Poland
    • Corresponding Author InformationCorresponding author.

Received 28 February 2010; received in revised form 13 August 2010; accepted 18 August 2010. published online 21 October 2010.

Abstract 

There is increasing evidence that mood disorders may derive from the impact of environmental pressure on genetically susceptible individuals. Stress-induced hippocampal plasticity has been implicated in depression. We studied hippocampal transcriptomes in strains of mice that display high (HA) and low (LA) swim stress-induced analgesia and that differ in emotional behaviors and responses to different classes of antidepressants. Chronic mild stress (CMS) affected expression of a number of genes common for both strains. CMS also produced strain specific changes in expression suggesting that hippocampal responses to stress depend on genotype. Considerably larger number of genes, biological processes, molecular functions, biochemical pathways, and gene networks were affected by CMS in LA than in HA mice. The results suggest that potential drug targets against detrimental effects of stress include glutamate transporters, and cholinergic, cholecystokinin (CCK), glucocorticoids, and thyroid hormones receptors. Furthermore, some biological processes evoked by stress and different between the strains, such as apoptosis, neurogenesis and chromatin modifications, may be responsible for the long-term, irreversible effects of stress and suggest a role for epigenetic regulation of mood related stress responses.

Keywords: Depression, Chronic stress, Hippocampus, Analgesia, Pain, Nociception, Gene expression, Microarrays, Mice

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PII: S0924-977X(10)00182-3

doi:10.1016/j.euroneuro.2010.08.004

European Neuropsychopharmacology
Volume 21, Issue 1 , Pages 45-62, January 2011