Cargando…
Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines
In comparison to conventional repetitive transcranial magnetic stimulation (rTMS), theta burst stimulation is stronger and more effective as a brain stimulation approach within short periods. Although this deep rTMS technique is being applied in treating neuropsychiatric disorders, few animal studie...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674917/ https://www.ncbi.nlm.nih.gov/pubmed/33250722 http://dx.doi.org/10.3389/fnint.2020.556839 |
_version_ | 1783611611356856320 |
---|---|
author | Yang, Liu Su, Yawen Guo, Fannv Zhang, Handi Zhao, Yinglin Huang, Qinjun Xu, Haiyun |
author_facet | Yang, Liu Su, Yawen Guo, Fannv Zhang, Handi Zhao, Yinglin Huang, Qinjun Xu, Haiyun |
author_sort | Yang, Liu |
collection | PubMed |
description | In comparison to conventional repetitive transcranial magnetic stimulation (rTMS), theta burst stimulation is stronger and more effective as a brain stimulation approach within short periods. Although this deep rTMS technique is being applied in treating neuropsychiatric disorders, few animal studies have attempted to clarify the neurobiological mechanisms underlying its beneficial effects. This animal study examined the effects of deep rTMS on the cuprizone-induced neuropathologic and behavioral anomalies and explored the underlying mechanism. Adolescent male C57BL/6 mice were fed a rodent chow without or with cuprizone (CPZ; 0.2% w/w) for 5 weeks. Another two groups of mice were subjected to deep rTMS or sham rTMS once a day during weeks 2–5 of the CPZ-feeding period. The behaviors of all mice were assessed after the withdrawal of CPZ before neuropathological and immunological analyses. Compared to the CNT group, mice in CPZ and CPZ + Sham groups showed deficits in social recognition and spatial working memory as well as anxiety-like behavior, in addition to myelin breakdown and OL loss in the corpus callosum (CC), caudate putamen, cerebral cortex, and hippocampus of the brain. Deep rTMS effectively reduced behavioral anomalies and blocked myelin breakdown and OL loss in CPZ-fed mice. Besides, it also dampened microglia activation at lesion sites and rectified cytokines levels (IL-1β, IL-6, and IL-10) in CPZ-affected regions. The most significant effect was seen in the cerebral cortex where alleviated neuropathology co-existed with less microglia activation and higher IL-10 level. These data provided experimental evidence for the beneficial effects of deep rTMS in CPZ-fed mice and revealed a neurobiological mechanism of the modality. |
format | Online Article Text |
id | pubmed-7674917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76749172020-11-26 Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines Yang, Liu Su, Yawen Guo, Fannv Zhang, Handi Zhao, Yinglin Huang, Qinjun Xu, Haiyun Front Integr Neurosci Neuroscience In comparison to conventional repetitive transcranial magnetic stimulation (rTMS), theta burst stimulation is stronger and more effective as a brain stimulation approach within short periods. Although this deep rTMS technique is being applied in treating neuropsychiatric disorders, few animal studies have attempted to clarify the neurobiological mechanisms underlying its beneficial effects. This animal study examined the effects of deep rTMS on the cuprizone-induced neuropathologic and behavioral anomalies and explored the underlying mechanism. Adolescent male C57BL/6 mice were fed a rodent chow without or with cuprizone (CPZ; 0.2% w/w) for 5 weeks. Another two groups of mice were subjected to deep rTMS or sham rTMS once a day during weeks 2–5 of the CPZ-feeding period. The behaviors of all mice were assessed after the withdrawal of CPZ before neuropathological and immunological analyses. Compared to the CNT group, mice in CPZ and CPZ + Sham groups showed deficits in social recognition and spatial working memory as well as anxiety-like behavior, in addition to myelin breakdown and OL loss in the corpus callosum (CC), caudate putamen, cerebral cortex, and hippocampus of the brain. Deep rTMS effectively reduced behavioral anomalies and blocked myelin breakdown and OL loss in CPZ-fed mice. Besides, it also dampened microglia activation at lesion sites and rectified cytokines levels (IL-1β, IL-6, and IL-10) in CPZ-affected regions. The most significant effect was seen in the cerebral cortex where alleviated neuropathology co-existed with less microglia activation and higher IL-10 level. These data provided experimental evidence for the beneficial effects of deep rTMS in CPZ-fed mice and revealed a neurobiological mechanism of the modality. Frontiers Media S.A. 2020-11-05 /pmc/articles/PMC7674917/ /pubmed/33250722 http://dx.doi.org/10.3389/fnint.2020.556839 Text en Copyright © 2020 Yang, Su, Guo, Zhang, Zhao, Huang and Xu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Yang, Liu Su, Yawen Guo, Fannv Zhang, Handi Zhao, Yinglin Huang, Qinjun Xu, Haiyun Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines |
title | Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines |
title_full | Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines |
title_fullStr | Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines |
title_full_unstemmed | Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines |
title_short | Deep rTMS Mitigates Behavioral and Neuropathologic Anomalies in Cuprizone-Exposed Mice Through Reducing Microglial Proinflammatory Cytokines |
title_sort | deep rtms mitigates behavioral and neuropathologic anomalies in cuprizone-exposed mice through reducing microglial proinflammatory cytokines |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674917/ https://www.ncbi.nlm.nih.gov/pubmed/33250722 http://dx.doi.org/10.3389/fnint.2020.556839 |
work_keys_str_mv | AT yangliu deeprtmsmitigatesbehavioralandneuropathologicanomaliesincuprizoneexposedmicethroughreducingmicroglialproinflammatorycytokines AT suyawen deeprtmsmitigatesbehavioralandneuropathologicanomaliesincuprizoneexposedmicethroughreducingmicroglialproinflammatorycytokines AT guofannv deeprtmsmitigatesbehavioralandneuropathologicanomaliesincuprizoneexposedmicethroughreducingmicroglialproinflammatorycytokines AT zhanghandi deeprtmsmitigatesbehavioralandneuropathologicanomaliesincuprizoneexposedmicethroughreducingmicroglialproinflammatorycytokines AT zhaoyinglin deeprtmsmitigatesbehavioralandneuropathologicanomaliesincuprizoneexposedmicethroughreducingmicroglialproinflammatorycytokines AT huangqinjun deeprtmsmitigatesbehavioralandneuropathologicanomaliesincuprizoneexposedmicethroughreducingmicroglialproinflammatorycytokines AT xuhaiyun deeprtmsmitigatesbehavioralandneuropathologicanomaliesincuprizoneexposedmicethroughreducingmicroglialproinflammatorycytokines |