Journal of Affective Disorders
Volume 65, Issue 2 , Pages 117-122, July 2001

Is lithium response related to Gsα levels in transformed lymphoblasts from subjects with bipolar disorder?

  • Martin Alda

      Affiliations

    • Department of Psychiatry, Dalhousie University, Halifax, Canada
    • Department of Psychiatry, University of Ottawa, Ottawa, Canada
  • ,
  • Dan Keller

      Affiliations

    • Department of Psychiatry and Behavioural Neurosciences, McMaster University, HSC-4N77A, 1200 Main St. W., Hamilton, Ontario, Canada
  • ,
  • Eva Grof

      Affiliations

    • Department of Psychiatry, University of Ottawa, Ottawa, Canada
  • ,
  • Gustavo Turecki

      Affiliations

    • Centre for Research in Neuroscience, McGill University, Montreal, Canada
  • ,
  • Patrizia Cavazzoni

      Affiliations

    • Department of Psychiatry, University of Ottawa, Ottawa, Canada
  • ,
  • Anne Duffy

      Affiliations

    • Department of Psychiatry, Dalhousie University, Halifax, Canada
  • ,
  • Guy A Rouleau

      Affiliations

    • Centre for Research in Neuroscience, McGill University, Montreal, Canada
  • ,
  • Paul Grof

      Affiliations

    • Department of Psychiatry, University of Ottawa, Ottawa, Canada
  • ,
  • L.Trevor Young

      Affiliations

    • Department of Psychiatry and Behavioural Neurosciences, McMaster University, HSC-4N77A, 1200 Main St. W., Hamilton, Ontario, Canada
    • Corresponding Author InformationCorresponding author. Tel.: +1-905-525-9140, ext. 22501; fax: +1-905-522-8804

Received 1 October 1999; accepted 5 January 2000.

Abstract 

Background: A series of studies from independent laboratories have found increased levels of Gsα in bipolar disorder in postmortem brain and peripheral blood cells. Long-term lithium administration blunts G-protein coupled cAMP signaling and may regulate Gsα levels. Methods: We measured Gsα in transformed lymphoblasts obtained from subjects with bipolar disorder and compared the findings with 23 age- and sex-matched controls. To reduce patient heterogeneity, we included only patients with an excellent response to lithium prophylaxis. Results: We found no differences in Gsα protein levels measured with immunoblotting. Gsα levels did not correlate with age, age of onset or duration of lithium therapy. Limitations: This study made use of transformed lymphoblasts, which may not fully represent changes that occur in regionalized brain tissue. Furthermore, the transformed lymphoblasts used in this study were acquired from a select group of bipolar disorder subjects that responded to lithium treatment. Lastly, consideration has to be given to the small sample size of the study. Conclusions: These results are consistent with recent observations suggesting that mood state and treatment effects may account at least in part for increased Gsα levels in bipolar disorder. Clinical relevance: This study suggests a need to further characterize biological phenotypes in subjects with mood disorders to enhance genetic studies.

Keywords:  Bipolar disorder, Lithium, G protein, Signal transduction, Biological marker

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PII: S0165-0327(00)00166-X

Journal of Affective Disorders
Volume 65, Issue 2 , Pages 117-122, July 2001