Methylation of OPRL1 mediates the effect of psychosocial stress on binge drinking in adolescents
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Beitragende
- King's College London (KCL)
- Medical Research Council (MRC)
- University of Camerino
- Universität Heidelberg
- Trinity College Dublin
- Universität Hamburg
- University of Montreal
- Commissariat à l’énergie atomique et aux énergies alternatives (CEA)
- Charité – Universitätsmedizin Berlin
- University of Vermont
- University of Nottingham
- Physikalisch-Technische Bundesanstalt
- INSERM - Institut national de la santé et de la recherche médicale
- University of Toronto
- Child Mind Institute, Inc.
- University College Dublin
- Uppsala University
Abstract
Background: Nociceptin is a key regulator linking environmental stress and alcohol drinking. In a genome-wide methylation analysis, we recently identified an association of a methylated region in the OPRL1 gene with alcohol-use disorders. Methods: Here, we investigate the biological basis of this observation by analysing psychosocial stressors, methylation of the OPRL1 gene, brain response during reward anticipation and alcohol drinking in 660 fourteen-year-old adolescents of the IMAGEN study. We validate our findings in marchigian sardinian (msP) alcohol-preferring rats that are genetically selected for increased alcohol drinking and stress sensitivity. Results: We found that low methylation levels in intron 1 of OPRL1 are associated with higher psychosocial stress and higher frequency of binge drinking, an effect mediated by OPRL1 methylation. In individuals with low methylation of OPRL1, frequency of binge drinking is associated with stronger BOLD response in the ventral striatum during reward anticipation. In msP rats, we found that stress results in increased alcohol intake and decreased methylation of OPRL1 in the nucleus accumbens. Conclusions: Our findings describe an epigenetic mechanism that helps to explain how psychosocial stress influences risky alcohol consumption and reward processing, thus contributing to the elucidation of biological mechanisms underlying risk for substance abuse.
Details
Originalsprache | Englisch |
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Seiten (von - bis) | 650-658 |
Seitenumfang | 9 |
Fachzeitschrift | Journal of Child Psychology and Psychiatry and Allied Disciplines |
Jahrgang | 59 |
Ausgabenummer | 6 |
Publikationsstatus | Elektronische Veröffentlichung vor Drucklegung - 2 Dez. 2017 |
Peer-Review-Status | Ja |
Externe IDs
PubMed | 29197086 |
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ORCID | /0000-0003-1477-5395/work/161409609 |
ORCID | /0000-0001-5398-5569/work/161409049 |
Schlagworte
ASJC Scopus Sachgebiete
Schlagwörter
- adolescence, binge drinking, nucleus accumbens, OPRL1 methylation, stressful life events