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Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation
Repetitive transcranial magnetic stimulation (TMS), when applied to the dorsolateral prefrontal cortex (dlPFC), treats depression. Therapeutic effects are hypothesized to arise from propagation of local dlPFC stimulation effects across distributed networks; however, the mechanisms of this remain unr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655825/ https://www.ncbi.nlm.nih.gov/pubmed/37982031 http://dx.doi.org/10.1038/s44220-023-00046-8 |
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author | Eldaief, Mark C. McMains, Stephanie Izquierdo-Garcia, David Daneshzand, Mohammad Nummenmaa, Aapo Braga, Rodrigo M. |
author_facet | Eldaief, Mark C. McMains, Stephanie Izquierdo-Garcia, David Daneshzand, Mohammad Nummenmaa, Aapo Braga, Rodrigo M. |
author_sort | Eldaief, Mark C. |
collection | PubMed |
description | Repetitive transcranial magnetic stimulation (TMS), when applied to the dorsolateral prefrontal cortex (dlPFC), treats depression. Therapeutic effects are hypothesized to arise from propagation of local dlPFC stimulation effects across distributed networks; however, the mechanisms of this remain unresolved. dlPFC contains representations of different networks. As such, dlPFC TMS may exert different effects depending on the network being stimulated. Here, to test this, we applied high-frequency TMS to two nearby dlPFC targets functionally embedded in distinct anti-correlated networks—the default and salience networks— in the same individuals in separate sessions. Local and distributed TMS effects were measured with combined (18)fluorodeoxyglucose positron emission tomography and functional magnetic resonance imaging. Identical TMS patterns caused opposing effects on local glucose metabolism: metabolism increased at the salience target following salience TMS but decreased at the default target following default TMS. At the distributed level, both conditions increased functional connectivity between the default and salience networks, with this effect being dramatically larger following default TMS. Metabolic and haemodynamic effects were also linked: across subjects, the magnitude of local metabolic changes correlated with the degree of functional connectivity changes. These results suggest that TMS effects upon dlPFC are network specific. They also invoke putative antidepressant mechanisms of TMS: network de-coupling. |
format | Online Article Text |
id | pubmed-10655825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-106558252023-11-17 Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation Eldaief, Mark C. McMains, Stephanie Izquierdo-Garcia, David Daneshzand, Mohammad Nummenmaa, Aapo Braga, Rodrigo M. Nat Ment Health Article Repetitive transcranial magnetic stimulation (TMS), when applied to the dorsolateral prefrontal cortex (dlPFC), treats depression. Therapeutic effects are hypothesized to arise from propagation of local dlPFC stimulation effects across distributed networks; however, the mechanisms of this remain unresolved. dlPFC contains representations of different networks. As such, dlPFC TMS may exert different effects depending on the network being stimulated. Here, to test this, we applied high-frequency TMS to two nearby dlPFC targets functionally embedded in distinct anti-correlated networks—the default and salience networks— in the same individuals in separate sessions. Local and distributed TMS effects were measured with combined (18)fluorodeoxyglucose positron emission tomography and functional magnetic resonance imaging. Identical TMS patterns caused opposing effects on local glucose metabolism: metabolism increased at the salience target following salience TMS but decreased at the default target following default TMS. At the distributed level, both conditions increased functional connectivity between the default and salience networks, with this effect being dramatically larger following default TMS. Metabolic and haemodynamic effects were also linked: across subjects, the magnitude of local metabolic changes correlated with the degree of functional connectivity changes. These results suggest that TMS effects upon dlPFC are network specific. They also invoke putative antidepressant mechanisms of TMS: network de-coupling. 2023-05 2023-05-01 /pmc/articles/PMC10655825/ /pubmed/37982031 http://dx.doi.org/10.1038/s44220-023-00046-8 Text en https://creativecommons.org/licenses/by/4.0/This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 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 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/) . Reprints and permissions information is available at www.nature.com/reprints (http://www.nature.com/reprints) . |
spellingShingle | Article Eldaief, Mark C. McMains, Stephanie Izquierdo-Garcia, David Daneshzand, Mohammad Nummenmaa, Aapo Braga, Rodrigo M. Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation |
title | Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation |
title_full | Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation |
title_fullStr | Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation |
title_full_unstemmed | Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation |
title_short | Network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation |
title_sort | network-specific metabolic and haemodynamic effects elicited by non-invasive brain stimulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655825/ https://www.ncbi.nlm.nih.gov/pubmed/37982031 http://dx.doi.org/10.1038/s44220-023-00046-8 |
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