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Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model
Deep-brain stimulation (DBS) is an effective treatment for patients suffering from otherwise therapy-resistant psychiatric disorders, including obsessive-compulsive disorder. Modulation of cortico-striatal circuits has been suggested as a mechanism of action. To gain mechanistic insight, we monitore...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477328/ https://www.ncbi.nlm.nih.gov/pubmed/37666830 http://dx.doi.org/10.1038/s41467-023-41026-x |
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author | van den Boom, Bastijn J. G. Elhazaz-Fernandez, Alfredo Rasmussen, Peter A. van Beest, Enny H. Parthasarathy, Aishwarya Denys, Damiaan Willuhn, Ingo |
author_facet | van den Boom, Bastijn J. G. Elhazaz-Fernandez, Alfredo Rasmussen, Peter A. van Beest, Enny H. Parthasarathy, Aishwarya Denys, Damiaan Willuhn, Ingo |
author_sort | van den Boom, Bastijn J. G. |
collection | PubMed |
description | Deep-brain stimulation (DBS) is an effective treatment for patients suffering from otherwise therapy-resistant psychiatric disorders, including obsessive-compulsive disorder. Modulation of cortico-striatal circuits has been suggested as a mechanism of action. To gain mechanistic insight, we monitored neuronal activity in cortico-striatal regions in a mouse model for compulsive behavior, while systematically varying clinically-relevant parameters of internal-capsule DBS. DBS showed dose-dependent effects on both brain and behavior: An increasing, yet balanced, number of excited and inhibited neurons was recruited, scattered throughout cortico-striatal regions, while excessive grooming decreased. Such neuronal recruitment did not alter basic brain function such as resting-state activity, and only occurred in awake animals, indicating a dependency on network activity. In addition to these widespread effects, we observed specific involvement of the medial orbitofrontal cortex in therapeutic outcomes, which was corroborated by optogenetic stimulation. Together, our findings provide mechanistic insight into how DBS exerts its therapeutic effects on compulsive behaviors. |
format | Online Article Text |
id | pubmed-10477328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104773282023-09-06 Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model van den Boom, Bastijn J. G. Elhazaz-Fernandez, Alfredo Rasmussen, Peter A. van Beest, Enny H. Parthasarathy, Aishwarya Denys, Damiaan Willuhn, Ingo Nat Commun Article Deep-brain stimulation (DBS) is an effective treatment for patients suffering from otherwise therapy-resistant psychiatric disorders, including obsessive-compulsive disorder. Modulation of cortico-striatal circuits has been suggested as a mechanism of action. To gain mechanistic insight, we monitored neuronal activity in cortico-striatal regions in a mouse model for compulsive behavior, while systematically varying clinically-relevant parameters of internal-capsule DBS. DBS showed dose-dependent effects on both brain and behavior: An increasing, yet balanced, number of excited and inhibited neurons was recruited, scattered throughout cortico-striatal regions, while excessive grooming decreased. Such neuronal recruitment did not alter basic brain function such as resting-state activity, and only occurred in awake animals, indicating a dependency on network activity. In addition to these widespread effects, we observed specific involvement of the medial orbitofrontal cortex in therapeutic outcomes, which was corroborated by optogenetic stimulation. Together, our findings provide mechanistic insight into how DBS exerts its therapeutic effects on compulsive behaviors. Nature Publishing Group UK 2023-09-04 /pmc/articles/PMC10477328/ /pubmed/37666830 http://dx.doi.org/10.1038/s41467-023-41026-x Text en © The Author(s) 2023 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 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 | Article van den Boom, Bastijn J. G. Elhazaz-Fernandez, Alfredo Rasmussen, Peter A. van Beest, Enny H. Parthasarathy, Aishwarya Denys, Damiaan Willuhn, Ingo Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model |
title | Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model |
title_full | Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model |
title_fullStr | Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model |
title_full_unstemmed | Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model |
title_short | Unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model |
title_sort | unraveling the mechanisms of deep-brain stimulation of the internal capsule in a mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477328/ https://www.ncbi.nlm.nih.gov/pubmed/37666830 http://dx.doi.org/10.1038/s41467-023-41026-x |
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