Cargando…
Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks
Memory formation and reinstatement are thought to lock to the hippocampal theta rhythm, predicting that encoding and retrieval processes appear rhythmic themselves. Here, we show that rhythmicity can be observed in behavioral responses from memory tasks, where participants indicate, using button pre...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639755/ https://www.ncbi.nlm.nih.gov/pubmed/34857748 http://dx.doi.org/10.1038/s41467-021-27323-3 |
_version_ | 1784609204288356352 |
---|---|
author | ter Wal, Marije Linde-Domingo, Juan Lifanov, Julia Roux, Frédéric Kolibius, Luca D. Gollwitzer, Stephanie Lang, Johannes Hamer, Hajo Rollings, David Sawlani, Vijay Chelvarajah, Ramesh Staresina, Bernhard Hanslmayr, Simon Wimber, Maria |
author_facet | ter Wal, Marije Linde-Domingo, Juan Lifanov, Julia Roux, Frédéric Kolibius, Luca D. Gollwitzer, Stephanie Lang, Johannes Hamer, Hajo Rollings, David Sawlani, Vijay Chelvarajah, Ramesh Staresina, Bernhard Hanslmayr, Simon Wimber, Maria |
author_sort | ter Wal, Marije |
collection | PubMed |
description | Memory formation and reinstatement are thought to lock to the hippocampal theta rhythm, predicting that encoding and retrieval processes appear rhythmic themselves. Here, we show that rhythmicity can be observed in behavioral responses from memory tasks, where participants indicate, using button presses, the timing of encoding and recall of cue-object associative memories. We find no evidence for rhythmicity in button presses for visual tasks using the same stimuli, or for questions about already retrieved objects. The oscillations for correctly remembered trials center in the slow theta frequency range (1-5 Hz). Using intracranial EEG recordings, we show that the memory task induces temporally extended phase consistency in hippocampal local field potentials at slow theta frequencies, but significantly more for remembered than forgotten trials, providing a potential mechanistic underpinning for the theta oscillations found in behavioral responses. |
format | Online Article Text |
id | pubmed-8639755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86397552021-12-15 Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks ter Wal, Marije Linde-Domingo, Juan Lifanov, Julia Roux, Frédéric Kolibius, Luca D. Gollwitzer, Stephanie Lang, Johannes Hamer, Hajo Rollings, David Sawlani, Vijay Chelvarajah, Ramesh Staresina, Bernhard Hanslmayr, Simon Wimber, Maria Nat Commun Article Memory formation and reinstatement are thought to lock to the hippocampal theta rhythm, predicting that encoding and retrieval processes appear rhythmic themselves. Here, we show that rhythmicity can be observed in behavioral responses from memory tasks, where participants indicate, using button presses, the timing of encoding and recall of cue-object associative memories. We find no evidence for rhythmicity in button presses for visual tasks using the same stimuli, or for questions about already retrieved objects. The oscillations for correctly remembered trials center in the slow theta frequency range (1-5 Hz). Using intracranial EEG recordings, we show that the memory task induces temporally extended phase consistency in hippocampal local field potentials at slow theta frequencies, but significantly more for remembered than forgotten trials, providing a potential mechanistic underpinning for the theta oscillations found in behavioral responses. Nature Publishing Group UK 2021-12-02 /pmc/articles/PMC8639755/ /pubmed/34857748 http://dx.doi.org/10.1038/s41467-021-27323-3 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 ter Wal, Marije Linde-Domingo, Juan Lifanov, Julia Roux, Frédéric Kolibius, Luca D. Gollwitzer, Stephanie Lang, Johannes Hamer, Hajo Rollings, David Sawlani, Vijay Chelvarajah, Ramesh Staresina, Bernhard Hanslmayr, Simon Wimber, Maria Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks |
title | Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks |
title_full | Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks |
title_fullStr | Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks |
title_full_unstemmed | Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks |
title_short | Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks |
title_sort | theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639755/ https://www.ncbi.nlm.nih.gov/pubmed/34857748 http://dx.doi.org/10.1038/s41467-021-27323-3 |
work_keys_str_mv | AT terwalmarije thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT lindedomingojuan thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT lifanovjulia thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT rouxfrederic thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT kolibiuslucad thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT gollwitzerstephanie thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT langjohannes thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT hamerhajo thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT rollingsdavid thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT sawlanivijay thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT chelvarajahramesh thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT staresinabernhard thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT hanslmayrsimon thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks AT wimbermaria thetarhythmicitygovernshumanbehaviorandhippocampalsignalsduringmemorydependenttasks |