Pharmacopsychiatry 2015; 48(04/05): 145-149
DOI: 10.1055/s-0035-1549946
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Lithium-induced Clock Gene Expression in Lymphoblastoid Cells of Bipolar Affective Patients

S. Kittel-Schneider
1   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Frankfurt, Frankfurt, Germany
,
S. Schreck
2   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Würzburg, Würzburg, Germany
,
C. Ziegler
2   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Würzburg, Würzburg, Germany
,
L. Weißflog
1   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Frankfurt, Frankfurt, Germany
,
M. Hilscher
2   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Würzburg, Würzburg, Germany
,
R. Schwarz
2   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Würzburg, Würzburg, Germany
,
L. Schnetzler
1   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Frankfurt, Frankfurt, Germany
,
M. Neuner
3   Department of Psychiatry, Community Hospital of Lohr, Lohr am Main, Germany
,
A. Reif
1   Department of Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Frankfurt, Frankfurt, Germany
› Author Affiliations
Further Information

Publication History

received 15 February 2015
revised 06 April 2015

accepted 17 April 2015

Publication Date:
26 May 2015 (online)

Abstract

Introduction: Disturbances of circadian rhythms occur in all episodes of bipolar disorder (BD). Lithium, as gold-standard in the maintenance treatment of BD, is known to influence circadian processes.

Methods: In a pilot study lymphoblastoid cell lines (LCLs) were generated from 8 BD patients and 6 healthy controls. The LCLs were treated with lithiumchloride (LiCl) for 3 weeks. Cell cycles were then synchronized and expressional analysis by quantitative Real Time PCR was done.

Results: BD and controls differed in the period length regarding DBP (albumin D-box binding protein) expression and DBP expression was also influenced by lithium treatment. Furthermore, baseline DBP expression was significantly different between non-treated BD and healthy controls. None of the other analyzed circadian genes showed to be influenced by chronic lithium treatment or to be differentially regulated due to the diagnosis.

Discussion: We here show that chronic lithium treatment of LCLs leads to decreased expression of the clock gene DBP, rendering DBP a lithium-regulated gene. We could confirm the role of the circadian clock as well in lithium mode of action as in the pathomechanisms of BD although future studies with a greater number of participants and cell lines are needed.

Supporting Information

 
  • References

  • 1 Etain B, Milhiet V, Bellivier F, Leboyer M. Genetics of circadian rhythms and mood spectrum disorders. Eur Neuropsychopharmacol 2011; 21 (Suppl. 04) S676-S682
  • 2 Grandin LD, Alloy LB, Abramson LY. The social zeitgeber theory, circadian rhythms, and mood disorders: review and evaluation. Clin Psychol Rev 2006; 26: 679-694
  • 3 Geddes JR, Miklowitz DJ. Treatment of bipolar disorder. Lancet 2013; 381: 1672-1682
  • 4 Wehr TA, Turner EH, Shimada JM et al. Treatment of rapidly cycling bipolar patient by using extended bed rest and darkness to stabilize the timing and duration of sleep. Biol Psychiatry 1998; 43: 822-828
  • 5 Takahashi JS, Hong HK, Ko CH et al. The genetics of mammalian circadian order and disorder: implications for physiology and disease. Nat Rev Genet 2008; 9: 764-775
  • 6 Mansour HA, Talkowski ME, Wood J et al. Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia. Bipolar Disord 2009; 11: 701-710
  • 7 Soria V, Martinez-Amoros E, Escaramis G et al. Differential association of circadian genes with mood disorders: CRY1 and NPAS2 are associated with unipolar major depression and CLOCK and VIP with bipolar disorder. Neuropsychopharmacology 2010; 35: 1279-1289
  • 8 McGrath CL, Glatt SJ, Sklar P et al. Evidence for genetic association of RORB with bipolar disorder. BMC Psychiatry 2009; 9: 70
  • 9 Nievergelt CM, Kripke DF, Barrett TB et al. Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder. Am J Med Genet B Neuropsychiatr Genet 2006; 141B: 234-241
  • 10 Shi J, Wittke-Thompson JK et al. Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm. Am J Med Genet B Neuropsychiatr Genet 2008; 147B: 1047-1055
  • 11 Yatham LN, Kennedy SH, Parikh SV et al. Canadian Network for Mood and Anxiety Treatments (CANMAT) and International Society for. Bipolar Disorders (ISBD) collaborative update of CANMAT guidelines for the management of patients with bipolar disorder: update 2013. Bipolar Disord 2013; 15: 1-44
  • 12 Pfennig A, Bschor T, Falkai P et al. The diagnosis and treatment of bipolar disorder: recommendations from the current s3 guideline. Dtsch Arztebl Int 2013; 110: 92-100
  • 13 O’Donnell KC, Gould TD. The behavioral actions of lithium in rodent models: leads to develop novel therapeutics. Neurosci Biobehav Rev 2007; 31: 932-962
  • 14 Abe M, Herzog ED, Block GD. Lithium lengthens the circadian period of individual suprachiasmatic nucleus neurons. Neuroreport 2000; 11: 3261-3264
  • 15 Iitaka C, Miyazaki K, Akaike T et al. A role for glycogen synthase kinase-3beta in the mammalian circadian clock. J Biol Chem 2005; 280: 29397-29402
  • 16 Sahar S, Zocchi L, Kinoshita C et al. Regulation of BMAL1 protein stability and circadian function by GSK3beta-mediated phosphorylation. PLoS One 2010; 5: e8561
  • 17 Li J, Lu WQ, Beesley S et al. Lithium impacts on the amplitude and period of the molecular circadian clockwork. PLoS One 2012; 7: e33292
  • 18 Roybal K, Theobold D, Graham A et al. Mania-like behavior induced by disruption of CLOCK. Proc Natl Acad Sci USA 2007; 104: 6406-6411
  • 19 Rybakowski JK. Response to Lithium in Bipolar Disorder: Clinical and Genetic Findings. ACS Chem Neurosci 2014;
  • 20 Bamne MN, Ponder CA, Wood JA et al. Application of an ex vivo cellular model of circadian variation for bipolar disorder research: a proof of concept study. Bipolar Disord 2013; 15: 694-700
  • 21 Pagani L, Semenova EA, Moriggi E et al. The physiological period length of the human circadian clock in vivo is directly proportional to period in human fibroblasts. PLoS One 2010; 5: e13376
  • 22 Osland TM, Ferno J, Havik B et al. Lithium differentially affects clock gene expression in serum-shocked NIH-3T3 cells. J Psychopharmacol 2011; 25: 924-933
  • 23 Fähndrich ES. R.-D. ed. Leitfaden zur Erfassung des psychopathologischen Befundes. Halbstrukturiertes Interview anhand des AMDP-Systems. Berlin: Hogrefe; 2007
  • 24 Margraf J. Diagnostisches Kurzinterview bei psychischen Störungen: Mini-DIPS. Berlin Heidelberg New York: Springer Verlag; 1994
  • 25 Griefahn B, Künemund C, Bröde P et al. The Validity of a German Version of the Morningness-Eveningness-Questionnaire Developed by Horne and Östberg. Somnologie 2001; 5 71-80
  • 26 Horne JA, Ostberg O. A self-assessment questionnaire to determine morningness-eveningness in human circadian rhythms. Int J Chronobiol 1976; 4: 97-110
  • 27 Gachon F, Olela FF, Schaad O et al. The circadian PAR-domain basic leucine zipper transcription factors DBP, TEF, and HLF modulate basal and inducible xenobiotic detoxification. Cell Metab 2006; 4: 25-36
  • 28 Mueller CR, Maire P, Schibler U. DBP, a liver-enriched transcriptional activator, is expressed late in ontogeny and its tissue specificity is determined posttranscriptionally. Cell 1990; 61: 279-291
  • 29 Mitsui S, Yamaguchi S, Matsuo T et al. Antagonistic role of E4BP4 and PAR proteins in the circadian oscillatory mechanism. Genes Dev 2001; 15: 995-1006
  • 30 Kim SH, Yu HS, Park HG et al. Egr1 regulates lithium-induced transcription of the Period 2 (PER2) gene. Biochim Biophys Acta 2013; 1832: 1969-1979
  • 31 Yang S, Van Dongen HP, Wang K et al. Assessment of circadian function in fibroblasts of patients with bipolar disorder. Mol Psychiatry 2009; 14: 143-155
  • 32 McCarthy MJ, Wei H, Marnoy Z et al. Genetic and clinical factors predict lithium’s effects on PER2 gene expression rhythms in cells from bipolar disorder patients. Transl Psychiatry 2013; 3: e318