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Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues
Drug addiction is a chronic relapsing disorder of compulsive drug use. Studies of the neurobehavioral factors that promote drug relapse have yet to produce an effective treatment. Here we take a different approach and examine the factors that suppress—rather than promote—relapse. Adapting Pavlovian...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718661/ https://www.ncbi.nlm.nih.gov/pubmed/31477694 http://dx.doi.org/10.1038/s41467-019-11799-1 |
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author | Laque, Amanda L. De Ness, Genna Wagner, Grant E. Nedelescu, Hermina Carroll, Ayla Watry, Debbie M. Kerr, Tony Koya, Eisuke Hope, Bruce T. Weiss, Friedbert Elmer, Greg I. Suto, Nobuyoshi |
author_facet | Laque, Amanda L. De Ness, Genna Wagner, Grant E. Nedelescu, Hermina Carroll, Ayla Watry, Debbie M. Kerr, Tony Koya, Eisuke Hope, Bruce T. Weiss, Friedbert Elmer, Greg I. Suto, Nobuyoshi |
author_sort | Laque, Amanda |
collection | PubMed |
description | Drug addiction is a chronic relapsing disorder of compulsive drug use. Studies of the neurobehavioral factors that promote drug relapse have yet to produce an effective treatment. Here we take a different approach and examine the factors that suppress—rather than promote—relapse. Adapting Pavlovian procedures to suppress operant drug response, we determined the anti-relapse action of environmental cues that signal drug omission (unavailability) in rats. Under laboratory conditions linked to compulsive drug use and heightened relapse risk, drug omission cues suppressed three major modes of relapse-promotion (drug-predictive cues, stress, and drug exposure) for cocaine and alcohol. This relapse-suppression is, in part, driven by omission cue-reactive neurons, which constitute small subsets of glutamatergic and GABAergic cells, in the infralimbic cortex. Future studies of such neural activity-based cellular units (neuronal ensembles/memory engram cells) for relapse-suppression can be used to identify alternate targets for addiction medicine through functional characterization of anti-relapse mechanisms. |
format | Online Article Text |
id | pubmed-6718661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67186612019-09-04 Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues Laque, Amanda L. De Ness, Genna Wagner, Grant E. Nedelescu, Hermina Carroll, Ayla Watry, Debbie M. Kerr, Tony Koya, Eisuke Hope, Bruce T. Weiss, Friedbert Elmer, Greg I. Suto, Nobuyoshi Nat Commun Article Drug addiction is a chronic relapsing disorder of compulsive drug use. Studies of the neurobehavioral factors that promote drug relapse have yet to produce an effective treatment. Here we take a different approach and examine the factors that suppress—rather than promote—relapse. Adapting Pavlovian procedures to suppress operant drug response, we determined the anti-relapse action of environmental cues that signal drug omission (unavailability) in rats. Under laboratory conditions linked to compulsive drug use and heightened relapse risk, drug omission cues suppressed three major modes of relapse-promotion (drug-predictive cues, stress, and drug exposure) for cocaine and alcohol. This relapse-suppression is, in part, driven by omission cue-reactive neurons, which constitute small subsets of glutamatergic and GABAergic cells, in the infralimbic cortex. Future studies of such neural activity-based cellular units (neuronal ensembles/memory engram cells) for relapse-suppression can be used to identify alternate targets for addiction medicine through functional characterization of anti-relapse mechanisms. Nature Publishing Group UK 2019-09-02 /pmc/articles/PMC6718661/ /pubmed/31477694 http://dx.doi.org/10.1038/s41467-019-11799-1 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 Laque, Amanda L. De Ness, Genna Wagner, Grant E. Nedelescu, Hermina Carroll, Ayla Watry, Debbie M. Kerr, Tony Koya, Eisuke Hope, Bruce T. Weiss, Friedbert Elmer, Greg I. Suto, Nobuyoshi Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues |
title | Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues |
title_full | Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues |
title_fullStr | Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues |
title_full_unstemmed | Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues |
title_short | Anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues |
title_sort | anti-relapse neurons in the infralimbic cortex of rats drive relapse-suppression by drug omission cues |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718661/ https://www.ncbi.nlm.nih.gov/pubmed/31477694 http://dx.doi.org/10.1038/s41467-019-11799-1 |
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