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Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex
The neural mechanisms underlying the effects of continuous Theta-Burst Stimulation (cTBS) in humans are poorly understood. Animal studies can clarify the effects of cTBS on individual neurons, but behavioral evidence is necessary to demonstrate the validity of the animal model. We investigated the b...
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/PMC7904760/ https://www.ncbi.nlm.nih.gov/pubmed/33627702 http://dx.doi.org/10.1038/s41598-021-83904-8 |
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author | Merken, Lara Davare, Marco Janssen, Peter Romero, Maria C. |
author_facet | Merken, Lara Davare, Marco Janssen, Peter Romero, Maria C. |
author_sort | Merken, Lara |
collection | PubMed |
description | The neural mechanisms underlying the effects of continuous Theta-Burst Stimulation (cTBS) in humans are poorly understood. Animal studies can clarify the effects of cTBS on individual neurons, but behavioral evidence is necessary to demonstrate the validity of the animal model. We investigated the behavioral effect of cTBS applied over parietal cortex in rhesus monkeys performing a visually-guided grasping task with two differently sized objects, which required either a power grip or a pad-to-side grip. We used Fitts’ law, predicting shorter grasping times (GT) for large compared to small objects, to investigate cTBS effects on two different grip types. cTBS induced long-lasting object-specific and dose-dependent changes in GT that remained present for up to two hours. High-intensity cTBS increased GTs for a power grip, but shortened GTs for a pad-to-side grip. Thus, high-intensity stimulation strongly reduced the natural GT difference between objects (i.e. the Fitts’ law effect). In contrast, low-intensity cTBS induced the opposite effects on GT. Modifying the coil orientation from the standard 45-degree to a 30-degree angle induced opposite cTBS effects on GT. These findings represent behavioral evidence for the validity of the nonhuman primate model to study the neural underpinnings of non-invasive brain stimulation. |
format | Online Article Text |
id | pubmed-7904760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79047602021-02-25 Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex Merken, Lara Davare, Marco Janssen, Peter Romero, Maria C. Sci Rep Article The neural mechanisms underlying the effects of continuous Theta-Burst Stimulation (cTBS) in humans are poorly understood. Animal studies can clarify the effects of cTBS on individual neurons, but behavioral evidence is necessary to demonstrate the validity of the animal model. We investigated the behavioral effect of cTBS applied over parietal cortex in rhesus monkeys performing a visually-guided grasping task with two differently sized objects, which required either a power grip or a pad-to-side grip. We used Fitts’ law, predicting shorter grasping times (GT) for large compared to small objects, to investigate cTBS effects on two different grip types. cTBS induced long-lasting object-specific and dose-dependent changes in GT that remained present for up to two hours. High-intensity cTBS increased GTs for a power grip, but shortened GTs for a pad-to-side grip. Thus, high-intensity stimulation strongly reduced the natural GT difference between objects (i.e. the Fitts’ law effect). In contrast, low-intensity cTBS induced the opposite effects on GT. Modifying the coil orientation from the standard 45-degree to a 30-degree angle induced opposite cTBS effects on GT. These findings represent behavioral evidence for the validity of the nonhuman primate model to study the neural underpinnings of non-invasive brain stimulation. Nature Publishing Group UK 2021-02-24 /pmc/articles/PMC7904760/ /pubmed/33627702 http://dx.doi.org/10.1038/s41598-021-83904-8 Text en © The Author(s) 2021 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 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/. |
spellingShingle | Article Merken, Lara Davare, Marco Janssen, Peter Romero, Maria C. Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex |
title | Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex |
title_full | Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex |
title_fullStr | Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex |
title_full_unstemmed | Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex |
title_short | Behavioral effects of continuous theta-burst stimulation in macaque parietal cortex |
title_sort | behavioral effects of continuous theta-burst stimulation in macaque parietal cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904760/ https://www.ncbi.nlm.nih.gov/pubmed/33627702 http://dx.doi.org/10.1038/s41598-021-83904-8 |
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