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Stress vulnerability shapes disruption of motor cortical neuroplasticity
Chronic stress is a major cause of neuropsychiatric conditions such as depression. Stress vulnerability varies individually in mice and humans, measured by behavioral changes. In contrast to affective symptoms, motor retardation as a consequence of stress is not well understood. We repeatedly imaged...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897461/ https://www.ncbi.nlm.nih.gov/pubmed/35246507 http://dx.doi.org/10.1038/s41398-022-01855-8 |
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author | Gellner, Anne-Kathrin Sitter, Aileen Rackiewicz, Michal Sylvester, Marc Philipsen, Alexandra Zimmer, Andreas Stein, Valentin |
author_facet | Gellner, Anne-Kathrin Sitter, Aileen Rackiewicz, Michal Sylvester, Marc Philipsen, Alexandra Zimmer, Andreas Stein, Valentin |
author_sort | Gellner, Anne-Kathrin |
collection | PubMed |
description | Chronic stress is a major cause of neuropsychiatric conditions such as depression. Stress vulnerability varies individually in mice and humans, measured by behavioral changes. In contrast to affective symptoms, motor retardation as a consequence of stress is not well understood. We repeatedly imaged dendritic spines of the motor cortex in Thy1-GFP M mice before and after chronic social defeat stress. Susceptible and resilient phenotypes were discriminated by symptom load and their motor learning abilities were assessed by a gross and fine motor task. Stress phenotypes presented individual short- and long-term changes in the hypothalamic–pituitary–adrenal axis as well as distinct patterns of altered motor learning. Importantly, stress was generally accompanied by a marked reduction of spine density in the motor cortex and spine dynamics depended on the stress phenotype. We found astrogliosis and altered microglia morphology along with increased microglia-neuron interaction in the motor cortex of susceptible mice. In cerebrospinal fluid, proteomic fingerprints link the behavioral changes and structural alterations in the brain to neurodegenerative disorders and dysregulated synaptic homeostasis. Our work emphasizes the importance of synaptic integrity and the risk of neurodegeneration within depression as a threat to brain health. |
format | Online Article Text |
id | pubmed-8897461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88974612022-03-22 Stress vulnerability shapes disruption of motor cortical neuroplasticity Gellner, Anne-Kathrin Sitter, Aileen Rackiewicz, Michal Sylvester, Marc Philipsen, Alexandra Zimmer, Andreas Stein, Valentin Transl Psychiatry Article Chronic stress is a major cause of neuropsychiatric conditions such as depression. Stress vulnerability varies individually in mice and humans, measured by behavioral changes. In contrast to affective symptoms, motor retardation as a consequence of stress is not well understood. We repeatedly imaged dendritic spines of the motor cortex in Thy1-GFP M mice before and after chronic social defeat stress. Susceptible and resilient phenotypes were discriminated by symptom load and their motor learning abilities were assessed by a gross and fine motor task. Stress phenotypes presented individual short- and long-term changes in the hypothalamic–pituitary–adrenal axis as well as distinct patterns of altered motor learning. Importantly, stress was generally accompanied by a marked reduction of spine density in the motor cortex and spine dynamics depended on the stress phenotype. We found astrogliosis and altered microglia morphology along with increased microglia-neuron interaction in the motor cortex of susceptible mice. In cerebrospinal fluid, proteomic fingerprints link the behavioral changes and structural alterations in the brain to neurodegenerative disorders and dysregulated synaptic homeostasis. Our work emphasizes the importance of synaptic integrity and the risk of neurodegeneration within depression as a threat to brain health. Nature Publishing Group UK 2022-03-04 /pmc/articles/PMC8897461/ /pubmed/35246507 http://dx.doi.org/10.1038/s41398-022-01855-8 Text en © The Author(s) 2022 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 | Article Gellner, Anne-Kathrin Sitter, Aileen Rackiewicz, Michal Sylvester, Marc Philipsen, Alexandra Zimmer, Andreas Stein, Valentin Stress vulnerability shapes disruption of motor cortical neuroplasticity |
title | Stress vulnerability shapes disruption of motor cortical neuroplasticity |
title_full | Stress vulnerability shapes disruption of motor cortical neuroplasticity |
title_fullStr | Stress vulnerability shapes disruption of motor cortical neuroplasticity |
title_full_unstemmed | Stress vulnerability shapes disruption of motor cortical neuroplasticity |
title_short | Stress vulnerability shapes disruption of motor cortical neuroplasticity |
title_sort | stress vulnerability shapes disruption of motor cortical neuroplasticity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897461/ https://www.ncbi.nlm.nih.gov/pubmed/35246507 http://dx.doi.org/10.1038/s41398-022-01855-8 |
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