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A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence

Alcohol use disorder is characterized by a high risk of relapse during periods of abstinence. Relapse is often triggered by retrieval of persistent alcohol memories upon exposure to alcohol-associated environmental cues, but little is known about the neuronal circuitry that supports the long-term st...

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Autores principales: Visser, Esther, Matos, Mariana R., van der Loo, Rolinka J., Marchant, Nathan J., de Vries, Taco J., Smit, August B., van den Oever, Michel C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202866/
https://www.ncbi.nlm.nih.gov/pubmed/32494694
http://dx.doi.org/10.1126/sciadv.aax7060
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author Visser, Esther
Matos, Mariana R.
van der Loo, Rolinka J.
Marchant, Nathan J.
de Vries, Taco J.
Smit, August B.
van den Oever, Michel C.
author_facet Visser, Esther
Matos, Mariana R.
van der Loo, Rolinka J.
Marchant, Nathan J.
de Vries, Taco J.
Smit, August B.
van den Oever, Michel C.
author_sort Visser, Esther
collection PubMed
description Alcohol use disorder is characterized by a high risk of relapse during periods of abstinence. Relapse is often triggered by retrieval of persistent alcohol memories upon exposure to alcohol-associated environmental cues, but little is known about the neuronal circuitry that supports the long-term storage of alcohol cue associations. We found that a small ensemble of neurons in the medial prefrontal cortex (mPFC) of mice was activated during cue-paired alcohol self-administration (SA) and that selective suppression of these neurons 1 month later attenuated cue-induced relapse to alcohol seeking. Inhibition of alcohol seeking was specific to these neurons as suppression of a non–alcohol-related or sucrose SA–activated mPFC ensemble did not affect relapse behavior. Hence, the mPFC neuronal ensemble activated during cue-paired alcohol consumption functions as a lasting memory trace that mediates cue-evoked relapse long after cessation of alcohol intake, thereby providing a potential target for treatment of alcohol relapse vulnerability.
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spelling pubmed-72028662020-06-02 A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence Visser, Esther Matos, Mariana R. van der Loo, Rolinka J. Marchant, Nathan J. de Vries, Taco J. Smit, August B. van den Oever, Michel C. Sci Adv Research Articles Alcohol use disorder is characterized by a high risk of relapse during periods of abstinence. Relapse is often triggered by retrieval of persistent alcohol memories upon exposure to alcohol-associated environmental cues, but little is known about the neuronal circuitry that supports the long-term storage of alcohol cue associations. We found that a small ensemble of neurons in the medial prefrontal cortex (mPFC) of mice was activated during cue-paired alcohol self-administration (SA) and that selective suppression of these neurons 1 month later attenuated cue-induced relapse to alcohol seeking. Inhibition of alcohol seeking was specific to these neurons as suppression of a non–alcohol-related or sucrose SA–activated mPFC ensemble did not affect relapse behavior. Hence, the mPFC neuronal ensemble activated during cue-paired alcohol consumption functions as a lasting memory trace that mediates cue-evoked relapse long after cessation of alcohol intake, thereby providing a potential target for treatment of alcohol relapse vulnerability. American Association for the Advancement of Science 2020-05-06 /pmc/articles/PMC7202866/ /pubmed/32494694 http://dx.doi.org/10.1126/sciadv.aax7060 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Visser, Esther
Matos, Mariana R.
van der Loo, Rolinka J.
Marchant, Nathan J.
de Vries, Taco J.
Smit, August B.
van den Oever, Michel C.
A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence
title A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence
title_full A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence
title_fullStr A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence
title_full_unstemmed A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence
title_short A persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence
title_sort persistent alcohol cue memory trace drives relapse to alcohol seeking after prolonged abstinence
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202866/
https://www.ncbi.nlm.nih.gov/pubmed/32494694
http://dx.doi.org/10.1126/sciadv.aax7060
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