Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Dependence-induced increase of alcohol self-administration and compulsive drinking mediated by the histone methyltransferase PRDM2

Title: Dependence-induced increase of alcohol self-administration and compulsive drinking mediated by the histone methyltransferase PRDM2
Authors: Barbier, Estelle; Johnstone, A. L.; Khomtchouk, B. B.; Tapocik, J. D.; Pitcairn, C.; Rehman, F.; Augier, Eric; Borich, A.; Schank, J. R.; Rienas, C. A.; Van Booven, D. J.; Sun, H.; Nätt, Daniel; Wahlestedt, C.; Heilig, Markus
Publisher Information: Linköpings universitet, Centrum för social och affektiv neurovetenskap; Linköpings universitet, Medicinska fakulteten; Region Östergötland, Psykiatriska kliniken; University of Miami, FL 33136 USA; NIAAA, MD USA; University of Georgia, GA 30602 USA; University of Miami, FL 33136 USA; University of Miami, FL 33136 USA; NATURE PUBLISHING GROUP
Publication Year: 2017
Collection: Linköping University Electronic Press (LiU E-Press)
Subject Terms: Neurosciences; Neurovetenskaper
Description: Epigenetic processes have been implicated in the pathophysiology of alcohol dependence, but the specific molecular mechanisms mediating dependence-induced neuroadaptations remain largely unknown. Here, we found that a history of alcohol dependence persistently decreased the expression of Prdm2, a histone methyltransferase that monomethylates histone 3 at the lysine 9 residue (H3K9me1), in the rat dorsomedial prefrontal cortex (dmPFC). Downregulation of Prdm2 was associated with decreased H3K9me1, supporting that changes in Prdm2 mRNA levels affected its activity. Chromatin immunoprecipitation followed by massively parallel DNA sequencing showed that genes involved in synaptic communication are epigenetically regulated by H3K9me1 in dependent rats. In non-dependent rats, viral-vector-mediated knockdown of Prdm2 in the dmPFC resulted in expression changes similar to those observed following a history of alcohol dependence. Prdm2 knockdown resulted in increased alcohol self-administration, increased aversion-resistant alcohol intake and enhanced stress-induced relapse to alcohol seeking, a phenocopy of postdependent rats. Collectively, these results identify a novel epigenetic mechanism that contributes to the development of alcohol-seeking behavior following a history of dependence. ; Funding Agencies|NIAAA division of Intramural Research; Swedish Research Council; NIAAA R01 [1R01AA023781-01A1]; United States Department of Defense (DoD), through the National Defense Science and Engineering Graduate Fellowship (NDSEG) Program; US National Institute of Health [DA035592, MH084880, NS071674]; DoD; Army Research Office (ARO); National Defense Science and Engineering Graduate (NDSEG) Fellowship [32 CFR 168a]
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: Molecular Psychiatry, 1359-4184, 2017, 22:12, s. 1746-1758; PMID 27573876; ISI:000416224100011
DOI: 10.1038/mp.2016.131
Availability: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-143625; https://doi.org/10.1038/mp.2016.131
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.2FFF270C
Database: BASE