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Cognitive functions and underlying parameters of human brain physiology are associated with chronotype
Circadian rhythms have natural relative variations among humans known as chronotype. Chronotype or being a morning or evening person, has a specific physiological, behavioural, and also genetic manifestation. Whether and how chronotype modulates human brain physiology and cognition is, however, not...
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/PMC8333420/ https://www.ncbi.nlm.nih.gov/pubmed/34344864 http://dx.doi.org/10.1038/s41467-021-24885-0 |
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author | Salehinejad, Mohammad Ali Wischnewski, Miles Ghanavati, Elham Mosayebi-Samani, Mohsen Kuo, Min-Fang Nitsche, Michael A. |
author_facet | Salehinejad, Mohammad Ali Wischnewski, Miles Ghanavati, Elham Mosayebi-Samani, Mohsen Kuo, Min-Fang Nitsche, Michael A. |
author_sort | Salehinejad, Mohammad Ali |
collection | PubMed |
description | Circadian rhythms have natural relative variations among humans known as chronotype. Chronotype or being a morning or evening person, has a specific physiological, behavioural, and also genetic manifestation. Whether and how chronotype modulates human brain physiology and cognition is, however, not well understood. Here we examine how cortical excitability, neuroplasticity, and cognition are associated with chronotype in early and late chronotype individuals. We monitor motor cortical excitability, brain stimulation-induced neuroplasticity, and examine motor learning and cognitive functions at circadian-preferred and non-preferred times of day in 32 individuals. Motor learning and cognitive performance (working memory, and attention) along with their electrophysiological components are significantly enhanced at the circadian-preferred, compared to the non-preferred time. This outperformance is associated with enhanced cortical excitability (prominent cortical facilitation, diminished cortical inhibition), and long-term potentiation/depression-like plasticity. Our data show convergent findings of how chronotype can modulate human brain functions from basic physiological mechanisms to behaviour and higher-order cognition. |
format | Online Article Text |
id | pubmed-8333420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83334202021-08-12 Cognitive functions and underlying parameters of human brain physiology are associated with chronotype Salehinejad, Mohammad Ali Wischnewski, Miles Ghanavati, Elham Mosayebi-Samani, Mohsen Kuo, Min-Fang Nitsche, Michael A. Nat Commun Article Circadian rhythms have natural relative variations among humans known as chronotype. Chronotype or being a morning or evening person, has a specific physiological, behavioural, and also genetic manifestation. Whether and how chronotype modulates human brain physiology and cognition is, however, not well understood. Here we examine how cortical excitability, neuroplasticity, and cognition are associated with chronotype in early and late chronotype individuals. We monitor motor cortical excitability, brain stimulation-induced neuroplasticity, and examine motor learning and cognitive functions at circadian-preferred and non-preferred times of day in 32 individuals. Motor learning and cognitive performance (working memory, and attention) along with their electrophysiological components are significantly enhanced at the circadian-preferred, compared to the non-preferred time. This outperformance is associated with enhanced cortical excitability (prominent cortical facilitation, diminished cortical inhibition), and long-term potentiation/depression-like plasticity. Our data show convergent findings of how chronotype can modulate human brain functions from basic physiological mechanisms to behaviour and higher-order cognition. Nature Publishing Group UK 2021-08-03 /pmc/articles/PMC8333420/ /pubmed/34344864 http://dx.doi.org/10.1038/s41467-021-24885-0 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 Salehinejad, Mohammad Ali Wischnewski, Miles Ghanavati, Elham Mosayebi-Samani, Mohsen Kuo, Min-Fang Nitsche, Michael A. Cognitive functions and underlying parameters of human brain physiology are associated with chronotype |
title | Cognitive functions and underlying parameters of human brain physiology are associated with chronotype |
title_full | Cognitive functions and underlying parameters of human brain physiology are associated with chronotype |
title_fullStr | Cognitive functions and underlying parameters of human brain physiology are associated with chronotype |
title_full_unstemmed | Cognitive functions and underlying parameters of human brain physiology are associated with chronotype |
title_short | Cognitive functions and underlying parameters of human brain physiology are associated with chronotype |
title_sort | cognitive functions and underlying parameters of human brain physiology are associated with chronotype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333420/ https://www.ncbi.nlm.nih.gov/pubmed/34344864 http://dx.doi.org/10.1038/s41467-021-24885-0 |
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