Literature DB >> 11849827

Analysis of gene expression with cDNA microarrays in rat brain after 7 and 42 days of oral lithium administration.

Francesca Bosetti1, Ruth Seemann, Jane M Bell, Robert Zahorchak, Elliott Friedman, Stanley I Rapoport, Pachiappan Manickam.   

Abstract

The gene expression profile in rat brain was examined using microarrays in rats fed lithium chloride for 7 days (subacute) or 42 days (chronic). Brain lithium concentrations were 0.39 mM and 0.79 mM (therapeutically relevant), at 7 and 42 days, respectively. Of the 4132 genes represented in the microarrays, 25 genes were downregulated by at least twofold and none was upregulated after 7 days of treatment. Expression of 50 genes was downregulated by at least two-fold at 42 days, without any being upregulated. Lithium treatment for 7 days did not affect at a measurable extent expression of 37 of the 50 genes that were downregulated at 42 days. Genes whose expression was changed at 42 days coded for a number of receptors, protein kinases, transcription and translation factors, markers of energy metabolism, and signal transduction. Thus, chronic lithium at a therapeutically relevant concentration reduced expression of a large number of genes involved in multiple signaling and other pathways, without increasing expression at a comparable extent.

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Year:  2002        PMID: 11849827     DOI: 10.1016/s0361-9230(01)00744-4

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  22 in total

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2.  Downregulation in components of the mitochondrial electron transport chain in the postmortem frontal cortex of subjects with bipolar disorder.

Authors:  Xiujun Sun; Jun-Feng Wang; Michael Tseng; L Trevor Young
Journal:  J Psychiatry Neurosci       Date:  2006-05       Impact factor: 6.186

3.  Inositol-related gene knockouts mimic lithium's effect on mitochondrial function.

Authors:  Lilach Toker; Yuly Bersudsky; Inbar Plaschkes; Vered Chalifa-Caspi; Gerard T Berry; Roberto Buccafusca; Dieder Moechars; R H Belmaker; Galila Agam
Journal:  Neuropsychopharmacology       Date:  2013-08-08       Impact factor: 7.853

4.  Chronic lithium chloride administration to rats elevates glucose metabolism in wide areas of brain, while potentiating negative effects on metabolism of dopamine D2-like receptor stimulation.

Authors:  Mireille Basselin; Lisa Chang; Stanley I Rapoport
Journal:  Psychopharmacology (Berl)       Date:  2006-06-20       Impact factor: 4.530

5.  Effects of Lithium Monotherapy for Bipolar Disorder on Gene Expression in Peripheral Lymphocytes.

Authors:  Amit Anand; Jeanette N McClintick; Jill Murrell; Harish Karne; John I Nurnberger; Howard J Edenberg
Journal:  Mol Neuropsychiatry       Date:  2016-06-29

6.  Chronic lithium feeding reduces upregulated brain arachidonic acid metabolism in HIV-1 transgenic rat.

Authors:  Epolia Ramadan; Mireille Basselin; Lisa Chang; Mei Chen; Kaizong Ma; Stanley I Rapoport
Journal:  J Neuroimmune Pharmacol       Date:  2012-07-04       Impact factor: 4.147

7.  Lithium reverses increased rates of cerebral protein synthesis in a mouse model of fragile X syndrome.

Authors:  Zhong-Hua Liu; Tianjian Huang; Carolyn Beebe Smith
Journal:  Neurobiol Dis       Date:  2011-12-29       Impact factor: 5.996

8.  Pharmacogenomics of mood stabilizers in the treatment of bipolar disorder.

Authors:  Alessio Squassina; Mirko Manchia; Maria Del Zompo
Journal:  Hum Genomics Proteomics       Date:  2010-08-03

Review 9.  Gene-environment interaction and the genetics of depression.

Authors:  Klaus Peter Lesch
Journal:  J Psychiatry Neurosci       Date:  2004-05       Impact factor: 6.186

10.  Lithium: a key to the genetics of bipolar disorder.

Authors:  Cristiana Cruceanu; Martin Alda; Gustavo Turecki
Journal:  Genome Med       Date:  2009-08-19       Impact factor: 11.117

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