Literature DB >> 18405950

Differential gene expression in the nucleus accumbens with ethanol self-administration in inbred alcohol-preferring rats.

Zachary A Rodd1, Mark W Kimpel, Howard J Edenberg, Richard L Bell, Wendy N Strother, Jeanette N McClintick, Lucinda G Carr, Tiebing Liang, William J McBride.   

Abstract

The current study examined the effects of operant ethanol (EtOH) self-administration on gene expression kin the nucleus accumbens (ACB) and amygdala (AMYG) of inbred alcohol-preferring (iP) rats. Rats self-trained on a standard two-lever operant paradigm to administer either water-water, EtOH (15% v/v)-water, or saccharin (SAC; 0.0125% g/v)-water. Animals were killed 24 h after the last operant session, and the ACB and AMYG dissected; RNA was extracted and purified for microarray analysis. For the ACB, there were 513 significant differences at the p<0.01 level in named genes: 55 between SAC and water; 215 between EtOH and water, and 243 between EtOH and SAC. In the case of the AMYG (p<0.01), there were 48 between SAC and water, 23 between EtOH and water, and 63 between EtOH and SAC group. Gene Ontology (GO) analysis indicated that differences in the ACB between the EtOH and SAC groups could be grouped into 15 significant (p<0.05) categories, which included major categories such as synaptic transmission, cell and ion homeostasis, and neurogenesis, whereas differences between the EtOH and water groups had only 4 categories, which also included homeostasis and synaptic transmission. Several genes were in common between the EtOH and both the SAC and water groups in the synaptic transmission (e.g., Cav2, Nrxn3, Gabrb2, Gad1, Homer1) and homeostasis (S100b, Prkca, Ftl1) categories. Overall, the results suggest that changes in gene expression in the ACB of iP rats are associated with the reinforcing effects of EtOH.

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Year:  2008        PMID: 18405950      PMCID: PMC4516281          DOI: 10.1016/j.pbb.2008.01.023

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  35 in total

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2.  The Gene Ontology (GO) database and informatics resource.

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Journal:  Alcohol Clin Exp Res       Date:  2001-08       Impact factor: 3.455

Review 10.  Neurocircuitry targets in ethanol reward and dependence.

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6.  Genome-wide gene expression analysis identifies K-ras as a regulator of alcohol intake.

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7.  Candidate genes for alcohol preference identified by expression profiling in alcohol-preferring and -nonpreferring reciprocal congenic rats.

Authors:  Tiebing Liang; Mark W Kimpel; Jeanette N McClintick; Ashley R Skillman; Kevin McCall; Howard J Edenberg; Lucinda G Carr
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8.  Changes in gene expression within the ventral tegmental area following repeated excessive binge-like alcohol drinking by alcohol-preferring (P) rats.

Authors:  William J McBride; Mark W Kimpel; Jeanette N McClintick; Zheng-Ming Ding; Sheketha R Hauser; Howard J Edenberg; Richard L Bell; Zachary A Rodd
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9.  Homer2 within the nucleus accumbens core bidirectionally regulates alcohol intake by both P and Wistar rats.

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10.  Ethanol is self-administered into the nucleus accumbens shell, but not the core: evidence of genetic sensitivity.

Authors:  Eric A Engleman; Zheng-Ming Ding; Scott M Oster; Jamie E Toalston; Richard L Bell; James M Murphy; William J McBride; Zachary A Rodd
Journal:  Alcohol Clin Exp Res       Date:  2009-09-17       Impact factor: 3.455

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