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Noradrenergic arousal after encoding reverses the course of systems consolidation in humans
It is commonly assumed that episodic memories undergo a time-dependent systems consolidation process, during which hippocampus-dependent memories eventually become reliant on neocortical areas. Here we show that systems consolidation dynamics can be experimentally manipulated and even reversed. We c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523710/ https://www.ncbi.nlm.nih.gov/pubmed/34663784 http://dx.doi.org/10.1038/s41467-021-26250-7 |
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author | Krenz, Valentina Sommer, Tobias Alink, Arjen Roozendaal, Benno Schwabe, Lars |
author_facet | Krenz, Valentina Sommer, Tobias Alink, Arjen Roozendaal, Benno Schwabe, Lars |
author_sort | Krenz, Valentina |
collection | PubMed |
description | It is commonly assumed that episodic memories undergo a time-dependent systems consolidation process, during which hippocampus-dependent memories eventually become reliant on neocortical areas. Here we show that systems consolidation dynamics can be experimentally manipulated and even reversed. We combined a single pharmacological elevation of post-encoding noradrenergic activity through the α(2)-adrenoceptor antagonist yohimbine with fMRI scanning both during encoding and recognition testing either 1 or 28 days later. We show that yohimbine administration, in contrast to placebo, leads to a time-dependent increase in hippocampal activity and multivariate encoding-retrieval pattern similarity, an indicator of episodic reinstatement, between 1 and 28 days. This is accompanied by a time-dependent decrease in neocortical activity. Behaviorally, these neural changes are linked to a reduced memory decline over time after yohimbine intake. These findings indicate that noradrenergic activity shortly after encoding may alter and even reverse systems consolidation in humans, thus maintaining vividness of memories over time. |
format | Online Article Text |
id | pubmed-8523710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85237102021-11-15 Noradrenergic arousal after encoding reverses the course of systems consolidation in humans Krenz, Valentina Sommer, Tobias Alink, Arjen Roozendaal, Benno Schwabe, Lars Nat Commun Article It is commonly assumed that episodic memories undergo a time-dependent systems consolidation process, during which hippocampus-dependent memories eventually become reliant on neocortical areas. Here we show that systems consolidation dynamics can be experimentally manipulated and even reversed. We combined a single pharmacological elevation of post-encoding noradrenergic activity through the α(2)-adrenoceptor antagonist yohimbine with fMRI scanning both during encoding and recognition testing either 1 or 28 days later. We show that yohimbine administration, in contrast to placebo, leads to a time-dependent increase in hippocampal activity and multivariate encoding-retrieval pattern similarity, an indicator of episodic reinstatement, between 1 and 28 days. This is accompanied by a time-dependent decrease in neocortical activity. Behaviorally, these neural changes are linked to a reduced memory decline over time after yohimbine intake. These findings indicate that noradrenergic activity shortly after encoding may alter and even reverse systems consolidation in humans, thus maintaining vividness of memories over time. Nature Publishing Group UK 2021-10-18 /pmc/articles/PMC8523710/ /pubmed/34663784 http://dx.doi.org/10.1038/s41467-021-26250-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Krenz, Valentina Sommer, Tobias Alink, Arjen Roozendaal, Benno Schwabe, Lars Noradrenergic arousal after encoding reverses the course of systems consolidation in humans |
title | Noradrenergic arousal after encoding reverses the course of systems consolidation in humans |
title_full | Noradrenergic arousal after encoding reverses the course of systems consolidation in humans |
title_fullStr | Noradrenergic arousal after encoding reverses the course of systems consolidation in humans |
title_full_unstemmed | Noradrenergic arousal after encoding reverses the course of systems consolidation in humans |
title_short | Noradrenergic arousal after encoding reverses the course of systems consolidation in humans |
title_sort | noradrenergic arousal after encoding reverses the course of systems consolidation in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523710/ https://www.ncbi.nlm.nih.gov/pubmed/34663784 http://dx.doi.org/10.1038/s41467-021-26250-7 |
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