{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Repunte-Canonigo V"],"funding":["NIDA NIH HHS","NIDDK NIH HHS","Medical Research Council","Department of Health","NIAAA NIH HHS"],"pagination":["1-10"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2925131"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["1339"],"pubmed_abstract":["Adaptations in the anterior cingulate cortex (ACC) have been implicated in alcohol and drug addiction. To identify genes that may contribute to excessive drinking, here we performed microarray analyses in laser microdissected rat ACC after a single or repeated administration of an intoxicating dose of alcohol (3 g/kg). Expression of the small G protein K-ras was differentially regulated following both single and repeated alcohol administration. We also observed that voluntary alcohol intake in K-ras heterozygous null mice (K-ras(+/-)) did not increase after withdrawal from repeated cycles of intermittent ethanol vapor exposure, unlike in their wild-type littermates. To identify K-ras regulated pathways, we then profiled gene expression in the ACC of K-ras(+/-), heterozygous null mice for the K-ras negative regulator Nf1 (Nf1(+/-)) and wild-type mice following repeated administration of an intoxicating dose of alcohol. Pathway analysis showed that alcohol differentially affected various pathways in a K-ras dependent manner - some of which previously shown to be regulated by alcohol - including the insulin/PI3K pathway, the NF-kappaB, the phosphodiesterases (PDEs) pathway, the Jak/Stat and the adipokine signaling pathways. Altogether, the data implicate K-ras-regulated pathways in the regulation of excessive alcohol drinking after a history of dependence."],"journal":["Brain research"],"pubmed_title":["Genome-wide gene expression analysis identifies K-ras as a regulator of alcohol intake."],"pmcid":["PMC2925131"],"funding_grant_id":["U01 AA013523","K99 AA016731","AA017371","AA01319","R01 AA017371-04","P50 AA006420","DA027129","G9817803B","R01 AA013191-05","AA013523","AA016731","R21 DA027129","R21 DK077616","AA006420","P50 AA006420-190014","R01 AA013191","DK077616","R00 AA016731","R01 AA017371"],"pubmed_authors":["Wagner U","Sanna PP","van der Stap LD","Roberts AJ","Chen J","Sabino V","Zorrilla EP","Repunte-Canonigo V","Schumann G"],"additional_accession":[]},"is_claimable":false,"name":"Genome-wide gene expression analysis identifies K-ras as a regulator of alcohol intake.","description":"Adaptations in the anterior cingulate cortex (ACC) have been implicated in alcohol and drug addiction. To identify genes that may contribute to excessive drinking, here we performed microarray analyses in laser microdissected rat ACC after a single or repeated administration of an intoxicating dose of alcohol (3 g/kg). Expression of the small G protein K-ras was differentially regulated following both single and repeated alcohol administration. We also observed that voluntary alcohol intake in K-ras heterozygous null mice (K-ras(+/-)) did not increase after withdrawal from repeated cycles of intermittent ethanol vapor exposure, unlike in their wild-type littermates. To identify K-ras regulated pathways, we then profiled gene expression in the ACC of K-ras(+/-), heterozygous null mice for the K-ras negative regulator Nf1 (Nf1(+/-)) and wild-type mice following repeated administration of an intoxicating dose of alcohol. Pathway analysis showed that alcohol differentially affected various pathways in a K-ras dependent manner - some of which previously shown to be regulated by alcohol - including the insulin/PI3K pathway, the NF-kappaB, the phosphodiesterases (PDEs) pathway, the Jak/Stat and the adipokine signaling pathways. Altogether, the data implicate K-ras-regulated pathways in the regulation of excessive alcohol drinking after a history of dependence.","dates":{"release":"2010-01-01T00:00:00Z","publication":"2010 Jun","modification":"2021-02-20T16:58:49Z","creation":"2019-03-27T00:33:28Z"},"accession":"S-EPMC2925131","cross_references":{"pubmed":["20388501"],"doi":["10.1016/j.brainres.2010.03.063"]}}