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Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression
Mood disorders are associated with elevated inflammation, and the reduction of symptoms after multiple treatments is often accompanied by pro-inflammation restoration. A variety of neuromodulation techniques that regulate regional brain activities have been used to treat refractory mood disorders. H...
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/PMC9829236/ https://www.ncbi.nlm.nih.gov/pubmed/36624089 http://dx.doi.org/10.1038/s41398-022-02297-y |
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author | Guo, Bingqi Zhang, Mengyao Hao, Wensi Wang, Yuping Zhang, Tingting Liu, Chunyan |
author_facet | Guo, Bingqi Zhang, Mengyao Hao, Wensi Wang, Yuping Zhang, Tingting Liu, Chunyan |
author_sort | Guo, Bingqi |
collection | PubMed |
description | Mood disorders are associated with elevated inflammation, and the reduction of symptoms after multiple treatments is often accompanied by pro-inflammation restoration. A variety of neuromodulation techniques that regulate regional brain activities have been used to treat refractory mood disorders. However, their efficacy varies from person to person and lack reliable indicator. This review summarizes clinical and animal studies on inflammation in neural circuits related to anxiety and depression and the evidence that neuromodulation therapies regulate neuroinflammation in the treatment of neurological diseases. Neuromodulation therapies, including transcranial magnetic stimulation (TMS), transcranial electrical stimulation (TES), electroconvulsive therapy (ECT), photobiomodulation (PBM), transcranial ultrasound stimulation (TUS), deep brain stimulation (DBS), and vagus nerve stimulation (VNS), all have been reported to attenuate neuroinflammation and reduce the release of pro-inflammatory factors, which may be one of the reasons for mood improvement. This review provides a better understanding of the effective mechanism of neuromodulation therapies and indicates that inflammatory biomarkers may serve as a reference for the assessment of pathological conditions and treatment options in anxiety and depression. |
format | Online Article Text |
id | pubmed-9829236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98292362023-01-10 Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression Guo, Bingqi Zhang, Mengyao Hao, Wensi Wang, Yuping Zhang, Tingting Liu, Chunyan Transl Psychiatry Review Article Mood disorders are associated with elevated inflammation, and the reduction of symptoms after multiple treatments is often accompanied by pro-inflammation restoration. A variety of neuromodulation techniques that regulate regional brain activities have been used to treat refractory mood disorders. However, their efficacy varies from person to person and lack reliable indicator. This review summarizes clinical and animal studies on inflammation in neural circuits related to anxiety and depression and the evidence that neuromodulation therapies regulate neuroinflammation in the treatment of neurological diseases. Neuromodulation therapies, including transcranial magnetic stimulation (TMS), transcranial electrical stimulation (TES), electroconvulsive therapy (ECT), photobiomodulation (PBM), transcranial ultrasound stimulation (TUS), deep brain stimulation (DBS), and vagus nerve stimulation (VNS), all have been reported to attenuate neuroinflammation and reduce the release of pro-inflammatory factors, which may be one of the reasons for mood improvement. This review provides a better understanding of the effective mechanism of neuromodulation therapies and indicates that inflammatory biomarkers may serve as a reference for the assessment of pathological conditions and treatment options in anxiety and depression. Nature Publishing Group UK 2023-01-09 /pmc/articles/PMC9829236/ /pubmed/36624089 http://dx.doi.org/10.1038/s41398-022-02297-y 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 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 | Review Article Guo, Bingqi Zhang, Mengyao Hao, Wensi Wang, Yuping Zhang, Tingting Liu, Chunyan Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression |
title | Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression |
title_full | Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression |
title_fullStr | Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression |
title_full_unstemmed | Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression |
title_short | Neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression |
title_sort | neuroinflammation mechanisms of neuromodulation therapies for anxiety and depression |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9829236/ https://www.ncbi.nlm.nih.gov/pubmed/36624089 http://dx.doi.org/10.1038/s41398-022-02297-y |
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