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Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans
Appetitive memories play a crucial role in learning and behavior, but under certain circumstances, such memories become maladaptive and play a vital role in addiction and other psychopathologies. Recent scientific research has demonstrated that memories can be modified following their reactivation t...
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/PMC6592881/ https://www.ncbi.nlm.nih.gov/pubmed/31239475 http://dx.doi.org/10.1038/s41598-019-45492-6 |
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author | Gera, Rani Barak, Segev Schonberg, Tom |
author_facet | Gera, Rani Barak, Segev Schonberg, Tom |
author_sort | Gera, Rani |
collection | PubMed |
description | Appetitive memories play a crucial role in learning and behavior, but under certain circumstances, such memories become maladaptive and play a vital role in addiction and other psychopathologies. Recent scientific research has demonstrated that memories can be modified following their reactivation through memory retrieval in a process termed memory reconsolidation. Several nonpharmacological behavioral manipulations yielded mixed results in their capacity to alter maladaptive memories in humans. Here, we aimed to translate the promising findings observed in rodents to humans. We constructed a novel three-day procedure using aversive counterconditioning to alter appetitive memories after short memory retrieval. On the first day, we used appetitive conditioning to form appetitive memories. On the second day, we retrieved these appetitive memories in one group (Retrieval group) but not in a second group. Subsequently, all participants underwent counterconditioning. On the third day, we attempted to reinstate the appetitive memories from day one. We observed a significant reduction in the reinstatement of the original appetitive memory when counterconditioning was induced following memory retrieval. Here, we provide a novel human paradigm that models several memory processes and demonstrate memory attenuation when counterconditioned after its retrieval. This paradigm can be used to study complex appetitive memory dynamics, e.g., memory reconsolidation and its underlying brain mechanisms. |
format | Online Article Text |
id | pubmed-6592881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65928812019-07-03 Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans Gera, Rani Barak, Segev Schonberg, Tom Sci Rep Article Appetitive memories play a crucial role in learning and behavior, but under certain circumstances, such memories become maladaptive and play a vital role in addiction and other psychopathologies. Recent scientific research has demonstrated that memories can be modified following their reactivation through memory retrieval in a process termed memory reconsolidation. Several nonpharmacological behavioral manipulations yielded mixed results in their capacity to alter maladaptive memories in humans. Here, we aimed to translate the promising findings observed in rodents to humans. We constructed a novel three-day procedure using aversive counterconditioning to alter appetitive memories after short memory retrieval. On the first day, we used appetitive conditioning to form appetitive memories. On the second day, we retrieved these appetitive memories in one group (Retrieval group) but not in a second group. Subsequently, all participants underwent counterconditioning. On the third day, we attempted to reinstate the appetitive memories from day one. We observed a significant reduction in the reinstatement of the original appetitive memory when counterconditioning was induced following memory retrieval. Here, we provide a novel human paradigm that models several memory processes and demonstrate memory attenuation when counterconditioned after its retrieval. This paradigm can be used to study complex appetitive memory dynamics, e.g., memory reconsolidation and its underlying brain mechanisms. Nature Publishing Group UK 2019-06-25 /pmc/articles/PMC6592881/ /pubmed/31239475 http://dx.doi.org/10.1038/s41598-019-45492-6 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 Gera, Rani Barak, Segev Schonberg, Tom Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans |
title | Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans |
title_full | Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans |
title_fullStr | Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans |
title_full_unstemmed | Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans |
title_short | Counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans |
title_sort | counterconditioning following memory retrieval diminishes the reinstatement of appetitive memories in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592881/ https://www.ncbi.nlm.nih.gov/pubmed/31239475 http://dx.doi.org/10.1038/s41598-019-45492-6 |
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