Cargando…

Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe

Memories are not stored in isolation. Insight into the relationship of initially unrelated events may trigger a flexible reconfiguration of the mnemonic representation of these events. Such representational changes allow the integration of events into coherent episodes and help to build up-to-date-m...

Descripción completa

Detalles Bibliográficos
Autores principales: Grob, Anna-Maria, Milivojevic, Branka, Alink, Arjen, Doeller, Christian F., Schwabe, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878442/
https://www.ncbi.nlm.nih.gov/pubmed/36503160
http://dx.doi.org/10.1016/j.neuroimage.2022.119804
_version_ 1784878485542535168
author Grob, Anna-Maria
Milivojevic, Branka
Alink, Arjen
Doeller, Christian F.
Schwabe, Lars
author_facet Grob, Anna-Maria
Milivojevic, Branka
Alink, Arjen
Doeller, Christian F.
Schwabe, Lars
author_sort Grob, Anna-Maria
collection PubMed
description Memories are not stored in isolation. Insight into the relationship of initially unrelated events may trigger a flexible reconfiguration of the mnemonic representation of these events. Such representational changes allow the integration of events into coherent episodes and help to build up-to-date-models of the world around us. This process is, however, frequently impaired in stress-related mental disorders resulting in symptoms such as fragmented memories in PTSD. Here, we combined a real life-like narrative-insight task, in which participants learned how initially separate events are linked, with fMRI-based representational similarity analysis to test if and how acute stress interferes with the insight-driven reconfiguration of memories. Our results showed that stress reduced the activity of medial temporal and prefrontal areas when participants gained insight into the link between events. Moreover, stress abolished the insight-related increase in representational dissimilarity for linked events in the anterior part of the hippocampus as well as its association with measures of subsequent memory that we observed in non-stressed controls. However, memory performance, as assessed in a forced-choice recognition test, was even enhanced in the stress group. Our findings suggest that acute stress impedes the neural integration of events into coherent episodes but promotes long-term memory for these integrated narratives and may thus have implications for understanding memory distortions in stress-related mental disorders.
format Online
Article
Text
id pubmed-9878442
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Academic Press
record_format MEDLINE/PubMed
spelling pubmed-98784422023-01-30 Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe Grob, Anna-Maria Milivojevic, Branka Alink, Arjen Doeller, Christian F. Schwabe, Lars Neuroimage Article Memories are not stored in isolation. Insight into the relationship of initially unrelated events may trigger a flexible reconfiguration of the mnemonic representation of these events. Such representational changes allow the integration of events into coherent episodes and help to build up-to-date-models of the world around us. This process is, however, frequently impaired in stress-related mental disorders resulting in symptoms such as fragmented memories in PTSD. Here, we combined a real life-like narrative-insight task, in which participants learned how initially separate events are linked, with fMRI-based representational similarity analysis to test if and how acute stress interferes with the insight-driven reconfiguration of memories. Our results showed that stress reduced the activity of medial temporal and prefrontal areas when participants gained insight into the link between events. Moreover, stress abolished the insight-related increase in representational dissimilarity for linked events in the anterior part of the hippocampus as well as its association with measures of subsequent memory that we observed in non-stressed controls. However, memory performance, as assessed in a forced-choice recognition test, was even enhanced in the stress group. Our findings suggest that acute stress impedes the neural integration of events into coherent episodes but promotes long-term memory for these integrated narratives and may thus have implications for understanding memory distortions in stress-related mental disorders. Academic Press 2023-01 /pmc/articles/PMC9878442/ /pubmed/36503160 http://dx.doi.org/10.1016/j.neuroimage.2022.119804 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Grob, Anna-Maria
Milivojevic, Branka
Alink, Arjen
Doeller, Christian F.
Schwabe, Lars
Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
title Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
title_full Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
title_fullStr Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
title_full_unstemmed Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
title_short Stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
title_sort stress disrupts insight-driven mnemonic reconfiguration in the medial temporal lobe
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878442/
https://www.ncbi.nlm.nih.gov/pubmed/36503160
http://dx.doi.org/10.1016/j.neuroimage.2022.119804
work_keys_str_mv AT grobannamaria stressdisruptsinsightdrivenmnemonicreconfigurationinthemedialtemporallobe
AT milivojevicbranka stressdisruptsinsightdrivenmnemonicreconfigurationinthemedialtemporallobe
AT alinkarjen stressdisruptsinsightdrivenmnemonicreconfigurationinthemedialtemporallobe
AT doellerchristianf stressdisruptsinsightdrivenmnemonicreconfigurationinthemedialtemporallobe
AT schwabelars stressdisruptsinsightdrivenmnemonicreconfigurationinthemedialtemporallobe