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Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms
Previous history of activity and learning modulates synaptic plasticity and can lead to saturation of synaptic connections. According to the synaptic homeostasis hypothesis, neural oscillations during slow-wave sleep play an important role in restoring plasticity within a functional range. However,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587974/ https://www.ncbi.nlm.nih.gov/pubmed/36173425 http://dx.doi.org/10.1007/s00221-022-06462-z |
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author | Bradley, Claire Elliott, Jessica Dudley, Samuel Kieseker, Genevieve A. Mattingley, Jason B. Sale, Martin V. |
author_facet | Bradley, Claire Elliott, Jessica Dudley, Samuel Kieseker, Genevieve A. Mattingley, Jason B. Sale, Martin V. |
author_sort | Bradley, Claire |
collection | PubMed |
description | Previous history of activity and learning modulates synaptic plasticity and can lead to saturation of synaptic connections. According to the synaptic homeostasis hypothesis, neural oscillations during slow-wave sleep play an important role in restoring plasticity within a functional range. However, it is not known whether slow-wave oscillations—without the concomitant requirement of sleep—play a causal role in human synaptic homeostasis. Here, we aimed to answer this question using transcranial alternating current stimulation (tACS) to induce slow-oscillatory activity in awake human participants. tACS was interleaved between two plasticity-inducing interventions: motor learning, and paired associative stimulation (PAS). The hypothesis tested was that slow-oscillatory tACS would prevent homeostatic interference between motor learning and PAS, and facilitate plasticity from these successive interventions. Thirty-six participants received sham and active fronto-motor tACS in two separate sessions, along with electroencephalography (EEG) recordings, while a further 38 participants received tACS through a control montage. Motor evoked potentials (MEPs) were recorded throughout the session to quantify plasticity changes after the different interventions, and the data were analysed with Bayesian statistics. As expected, there was converging evidence that motor training led to excitatory plasticity. Importantly, we found moderate evidence against an effect of active tACS in restoring PAS plasticity, and no evidence of lasting entrainment of slow oscillations in the EEG. This suggests that, under the conditions tested here, slow-oscillatory tACS does not modulate synaptic homeostasis in the motor system of awake humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00221-022-06462-z. |
format | Online Article Text |
id | pubmed-9587974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-95879742022-10-24 Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms Bradley, Claire Elliott, Jessica Dudley, Samuel Kieseker, Genevieve A. Mattingley, Jason B. Sale, Martin V. Exp Brain Res Research Article Previous history of activity and learning modulates synaptic plasticity and can lead to saturation of synaptic connections. According to the synaptic homeostasis hypothesis, neural oscillations during slow-wave sleep play an important role in restoring plasticity within a functional range. However, it is not known whether slow-wave oscillations—without the concomitant requirement of sleep—play a causal role in human synaptic homeostasis. Here, we aimed to answer this question using transcranial alternating current stimulation (tACS) to induce slow-oscillatory activity in awake human participants. tACS was interleaved between two plasticity-inducing interventions: motor learning, and paired associative stimulation (PAS). The hypothesis tested was that slow-oscillatory tACS would prevent homeostatic interference between motor learning and PAS, and facilitate plasticity from these successive interventions. Thirty-six participants received sham and active fronto-motor tACS in two separate sessions, along with electroencephalography (EEG) recordings, while a further 38 participants received tACS through a control montage. Motor evoked potentials (MEPs) were recorded throughout the session to quantify plasticity changes after the different interventions, and the data were analysed with Bayesian statistics. As expected, there was converging evidence that motor training led to excitatory plasticity. Importantly, we found moderate evidence against an effect of active tACS in restoring PAS plasticity, and no evidence of lasting entrainment of slow oscillations in the EEG. This suggests that, under the conditions tested here, slow-oscillatory tACS does not modulate synaptic homeostasis in the motor system of awake humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00221-022-06462-z. Springer Berlin Heidelberg 2022-09-29 2022 /pmc/articles/PMC9587974/ /pubmed/36173425 http://dx.doi.org/10.1007/s00221-022-06462-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Bradley, Claire Elliott, Jessica Dudley, Samuel Kieseker, Genevieve A. Mattingley, Jason B. Sale, Martin V. Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms |
title | Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms |
title_full | Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms |
title_fullStr | Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms |
title_full_unstemmed | Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms |
title_short | Slow-oscillatory tACS does not modulate human motor cortical response to repeated plasticity paradigms |
title_sort | slow-oscillatory tacs does not modulate human motor cortical response to repeated plasticity paradigms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587974/ https://www.ncbi.nlm.nih.gov/pubmed/36173425 http://dx.doi.org/10.1007/s00221-022-06462-z |
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