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A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder
Although epidemiological research has shown an increase in drinking following stressors and trauma, limited paradigms have been validated to study the relationship between stress and drinking in the human laboratory. The current study developed a progressive ratio (PR) operant procedure to examine t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645206/ https://www.ncbi.nlm.nih.gov/pubmed/28419649 http://dx.doi.org/10.1111/adb.12511 |
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author | McCaul, Mary E. Wand, Gary S. Weerts, Elise M. Xu, Xiaoqiang |
author_facet | McCaul, Mary E. Wand, Gary S. Weerts, Elise M. Xu, Xiaoqiang |
author_sort | McCaul, Mary E. |
collection | PubMed |
description | Although epidemiological research has shown an increase in drinking following stressors and trauma, limited paradigms have been validated to study the relationship between stress and drinking in the human laboratory. The current study developed a progressive ratio (PR) operant procedure to examine the effects of psychosocial stress on alcohol craving and several alcohol‐motivated behaviors in persons with alcohol use disorder. Current heavy, nontreatment‐seeking drinkers (N = 30) were media‐recruited and completed a comprehensive assessment of recent drinking, mood and health. Participants were admitted to the clinical research unit and underwent 4‐day, physician‐monitored alcohol abstinence. On days 4 and 5, participants underwent the Trier Social Stress Test or a neutral session in random order followed by the alcohol‐motivated response (AMR) procedure in which subjects worked for money or alcohol under a PR operant procedure. Subjects received earned money vouchers or alcohol at the conclusion of the session. The Trier Social Stress Test increased alcohol craving and rate of responding and decreased the number of changeovers between alcohol versus money reinforcers on the PR schedule. There was a positive relationship between alcohol craving and drinks earned during the stress session. This novel paradigm provides an experimental platform to examine motivation to drink without confounding by actual alcohol ingestion during the work session, thereby setting the stage for future studies of alcohol interventions. |
format | Online Article Text |
id | pubmed-5645206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56452062018-03-12 A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder McCaul, Mary E. Wand, Gary S. Weerts, Elise M. Xu, Xiaoqiang Addict Biol Human Experimental Study Although epidemiological research has shown an increase in drinking following stressors and trauma, limited paradigms have been validated to study the relationship between stress and drinking in the human laboratory. The current study developed a progressive ratio (PR) operant procedure to examine the effects of psychosocial stress on alcohol craving and several alcohol‐motivated behaviors in persons with alcohol use disorder. Current heavy, nontreatment‐seeking drinkers (N = 30) were media‐recruited and completed a comprehensive assessment of recent drinking, mood and health. Participants were admitted to the clinical research unit and underwent 4‐day, physician‐monitored alcohol abstinence. On days 4 and 5, participants underwent the Trier Social Stress Test or a neutral session in random order followed by the alcohol‐motivated response (AMR) procedure in which subjects worked for money or alcohol under a PR operant procedure. Subjects received earned money vouchers or alcohol at the conclusion of the session. The Trier Social Stress Test increased alcohol craving and rate of responding and decreased the number of changeovers between alcohol versus money reinforcers on the PR schedule. There was a positive relationship between alcohol craving and drinks earned during the stress session. This novel paradigm provides an experimental platform to examine motivation to drink without confounding by actual alcohol ingestion during the work session, thereby setting the stage for future studies of alcohol interventions. John Wiley and Sons Inc. 2017-04-17 2018-03 /pmc/articles/PMC5645206/ /pubmed/28419649 http://dx.doi.org/10.1111/adb.12511 Text en © 2017 The Authors.Addiction Biology published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Human Experimental Study McCaul, Mary E. Wand, Gary S. Weerts, Elise M. Xu, Xiaoqiang A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder |
title | A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder |
title_full | A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder |
title_fullStr | A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder |
title_full_unstemmed | A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder |
title_short | A paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder |
title_sort | paradigm for examining stress effects on alcohol‐motivated behaviors in participants with alcohol use disorder |
topic | Human Experimental Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645206/ https://www.ncbi.nlm.nih.gov/pubmed/28419649 http://dx.doi.org/10.1111/adb.12511 |
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