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Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories
Maladaptive reward memories (MRMs) are involved in the development and maintenance of acquired overconsumption disorders, such as harmful alcohol and drug use. The process of memory reconsolidation - where stored memories become briefly labile upon retrieval - may offer a means to disrupt MRMs and p...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879579/ https://www.ncbi.nlm.nih.gov/pubmed/31772157 http://dx.doi.org/10.1038/s41467-019-13162-w |
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author | Das, Ravi K. Gale, Grace Walsh, Katie Hennessy, Vanessa E. Iskandar, Georges Mordecai, Luke A. Brandner, Brigitta Kindt, Merel Curran, H. Valerie Kamboj, Sunjeev K. |
author_facet | Das, Ravi K. Gale, Grace Walsh, Katie Hennessy, Vanessa E. Iskandar, Georges Mordecai, Luke A. Brandner, Brigitta Kindt, Merel Curran, H. Valerie Kamboj, Sunjeev K. |
author_sort | Das, Ravi K. |
collection | PubMed |
description | Maladaptive reward memories (MRMs) are involved in the development and maintenance of acquired overconsumption disorders, such as harmful alcohol and drug use. The process of memory reconsolidation - where stored memories become briefly labile upon retrieval - may offer a means to disrupt MRMs and prevent relapse. However, reliable means for pharmacologically weakening MRMs in humans remain elusive. Here we demonstrate that the N-methyl D-aspartate (NMDA) antagonist ketamine is able to disrupt MRMs in hazardous drinkers when administered immediately after their retrieval. MRM retrieval + ketamine (RET + KET) effectively reduced the reinforcing effects of alcohol and long-term drinking levels, compared to ketamine or retrieval alone. Blood concentrations of ketamine and its metabolites during the critical ‘reconsolidation window’ predicted beneficial changes only following MRM reactivation. Pharmacological reconsolidation interference may provide a means to rapidly rewrite maladaptive memory and should be further pursued in alcohol and drug use disorders. |
format | Online Article Text |
id | pubmed-6879579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68795792019-11-29 Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories Das, Ravi K. Gale, Grace Walsh, Katie Hennessy, Vanessa E. Iskandar, Georges Mordecai, Luke A. Brandner, Brigitta Kindt, Merel Curran, H. Valerie Kamboj, Sunjeev K. Nat Commun Article Maladaptive reward memories (MRMs) are involved in the development and maintenance of acquired overconsumption disorders, such as harmful alcohol and drug use. The process of memory reconsolidation - where stored memories become briefly labile upon retrieval - may offer a means to disrupt MRMs and prevent relapse. However, reliable means for pharmacologically weakening MRMs in humans remain elusive. Here we demonstrate that the N-methyl D-aspartate (NMDA) antagonist ketamine is able to disrupt MRMs in hazardous drinkers when administered immediately after their retrieval. MRM retrieval + ketamine (RET + KET) effectively reduced the reinforcing effects of alcohol and long-term drinking levels, compared to ketamine or retrieval alone. Blood concentrations of ketamine and its metabolites during the critical ‘reconsolidation window’ predicted beneficial changes only following MRM reactivation. Pharmacological reconsolidation interference may provide a means to rapidly rewrite maladaptive memory and should be further pursued in alcohol and drug use disorders. Nature Publishing Group UK 2019-11-26 /pmc/articles/PMC6879579/ /pubmed/31772157 http://dx.doi.org/10.1038/s41467-019-13162-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Das, Ravi K. Gale, Grace Walsh, Katie Hennessy, Vanessa E. Iskandar, Georges Mordecai, Luke A. Brandner, Brigitta Kindt, Merel Curran, H. Valerie Kamboj, Sunjeev K. Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories |
title | Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories |
title_full | Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories |
title_fullStr | Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories |
title_full_unstemmed | Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories |
title_short | Ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories |
title_sort | ketamine can reduce harmful drinking by pharmacologically rewriting drinking memories |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879579/ https://www.ncbi.nlm.nih.gov/pubmed/31772157 http://dx.doi.org/10.1038/s41467-019-13162-w |
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