Literature DB >> 16710313

Identifying genes in monoamine nuclei that may determine stress vulnerability and depressive behavior in Wistar-Kyoto rats.

Kimberly A Pearson1, Alisson Stephen, Sheryl G Beck, Rita J Valentino.   

Abstract

The Wistar-Kyoto (WKY) rat is stress sensitive and exhibits depressive-like behavior. The locus coeruleus (LC)-norepinephrine and dorsal raphe (DR)-serotonin systems mediate certain aspects of the stress response and have been implicated in depression. Microarray technology was used to identify gene expression differences in the LC and DR between WKY vs Sprague-Dawley (SD) rats that might account for the WKY phenotype. RNA was isolated from microdissected LC and DR, amplified, and hybridized to microarrays (1 array/subject, n = 4/group). Significance of microarray (SAM) analysis revealed increased expression of 66 genes in the LC and 19 genes in the DR and decreased expression of 33 genes in the DR of WKY rats. Hierarchical clustering identified differences in gene expression profiles of WKY vs SD rats that generally concurred with SAM. Notably, genes that encoded for enzymes involved in norepinephrine turnover, amino-acid receptors, and certain G-protein-coupled receptors were elevated in the LC of WKY rats. The DR of WKY rats showed decreased expression of genes encoding several potassium channels and neurofilament genes. The chromosomal locations of 15 genes that were differentially expressed in WKY rats were near loci identified as contributing to depressive-like behaviors in the rat. The specific genes revealed by the present analysis as being differentially expressed in WKY rats may contribute to their unique behavioral profile and suggest targets that confer susceptibility to stress-related psychiatric disorders.

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Year:  2006        PMID: 16710313      PMCID: PMC2836184          DOI: 10.1038/sj.npp.1301100

Source DB:  PubMed          Journal:  Neuropsychopharmacology        ISSN: 0893-133X            Impact factor:   7.853


  71 in total

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4.  Learning behavior, escape behavior, and depression in an ulcer susceptible rat strain.

Authors:  W P Paré
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10.  Effect of repeated novel stressors on depressive behavior and brain norepinephrine receptor system in Sprague-Dawley and Wistar Kyoto (WKY) rats.

Authors:  S M Tejani-Butt; W P Paré; J Yang
Journal:  Brain Res       Date:  1994-06-27       Impact factor: 3.252

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  19 in total

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Review 7.  Gene expression studies in major depression.

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8.  Expression profiling of a genetic animal model of depression reveals novel molecular pathways underlying depressive-like behaviours.

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9.  Antidepressant-like effects of kappa-opioid receptor antagonists in Wistar Kyoto rats.

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10.  Sleep active cortical neurons expressing neuronal nitric oxide synthase are active after both acute sleep deprivation and chronic sleep restriction.

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