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Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by cognitive decline and brain neuronal loss. A pioneering field of research in AD is brain stimulation via electromagnetic fields (EMFs), which may produce clinical benefits. Noninvasive brain stimulation techniques, such a...

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Autores principales: Bashir, Shahid, Uzair, Mohammad, Abualait, Turki, Arshad, Muhammad, Khallaf, Roaa A., Niaz, Asim, Thani, Ziyad, Yoo, Woo-Kyoung, Túnez, Isaac, Demirtas-Tatlidede, Asli, Meo, Sultan Ayoub
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845030/
https://www.ncbi.nlm.nih.gov/pubmed/35119081
http://dx.doi.org/10.3892/mmr.2022.12625
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author Bashir, Shahid
Uzair, Mohammad
Abualait, Turki
Arshad, Muhammad
Khallaf, Roaa A.
Niaz, Asim
Thani, Ziyad
Yoo, Woo-Kyoung
Túnez, Isaac
Demirtas-Tatlidede, Asli
Meo, Sultan Ayoub
author_facet Bashir, Shahid
Uzair, Mohammad
Abualait, Turki
Arshad, Muhammad
Khallaf, Roaa A.
Niaz, Asim
Thani, Ziyad
Yoo, Woo-Kyoung
Túnez, Isaac
Demirtas-Tatlidede, Asli
Meo, Sultan Ayoub
author_sort Bashir, Shahid
collection PubMed
description Alzheimer's disease (AD) is a neurodegenerative disorder characterized by cognitive decline and brain neuronal loss. A pioneering field of research in AD is brain stimulation via electromagnetic fields (EMFs), which may produce clinical benefits. Noninvasive brain stimulation techniques, such as transcranial magnetic stimulation (TMS), have been developed to treat neurological and psychiatric disorders. The purpose of the present review is to identify neurobiological changes, including inflammatory, neurodegenerative, apoptotic, neuroprotective and genetic changes, which are associated with repetitive TMS (rTMS) treatment in patients with AD. Furthermore, it aims to evaluate the effect of TMS treatment in patients with AD and to identify the associated mechanisms. The present review highlights the changes in inflammatory and apoptotic mechanisms, mitochondrial enzymatic activities, and modulation of gene expression (microRNA expression profiles) associated with rTMS or sham procedures. At the molecular level, it has been suggested that EMFs generated by TMS may affect the cell redox status and amyloidogenic processes. TMS may also modulate gene expression by acting on both transcriptional and post-transcriptional regulatory mechanisms. TMS may increase brain cortical excitability, induce specific potentiation phenomena, and promote synaptic plasticity and recovery of impaired functions; thus, it may re-establish cognitive performance in patients with AD.
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spelling pubmed-88450302022-03-02 Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease Bashir, Shahid Uzair, Mohammad Abualait, Turki Arshad, Muhammad Khallaf, Roaa A. Niaz, Asim Thani, Ziyad Yoo, Woo-Kyoung Túnez, Isaac Demirtas-Tatlidede, Asli Meo, Sultan Ayoub Mol Med Rep Review Alzheimer's disease (AD) is a neurodegenerative disorder characterized by cognitive decline and brain neuronal loss. A pioneering field of research in AD is brain stimulation via electromagnetic fields (EMFs), which may produce clinical benefits. Noninvasive brain stimulation techniques, such as transcranial magnetic stimulation (TMS), have been developed to treat neurological and psychiatric disorders. The purpose of the present review is to identify neurobiological changes, including inflammatory, neurodegenerative, apoptotic, neuroprotective and genetic changes, which are associated with repetitive TMS (rTMS) treatment in patients with AD. Furthermore, it aims to evaluate the effect of TMS treatment in patients with AD and to identify the associated mechanisms. The present review highlights the changes in inflammatory and apoptotic mechanisms, mitochondrial enzymatic activities, and modulation of gene expression (microRNA expression profiles) associated with rTMS or sham procedures. At the molecular level, it has been suggested that EMFs generated by TMS may affect the cell redox status and amyloidogenic processes. TMS may also modulate gene expression by acting on both transcriptional and post-transcriptional regulatory mechanisms. TMS may increase brain cortical excitability, induce specific potentiation phenomena, and promote synaptic plasticity and recovery of impaired functions; thus, it may re-establish cognitive performance in patients with AD. D.A. Spandidos 2022-04 2022-02-01 /pmc/articles/PMC8845030/ /pubmed/35119081 http://dx.doi.org/10.3892/mmr.2022.12625 Text en Copyright: © Bashir et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Bashir, Shahid
Uzair, Mohammad
Abualait, Turki
Arshad, Muhammad
Khallaf, Roaa A.
Niaz, Asim
Thani, Ziyad
Yoo, Woo-Kyoung
Túnez, Isaac
Demirtas-Tatlidede, Asli
Meo, Sultan Ayoub
Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease
title Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease
title_full Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease
title_fullStr Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease
title_full_unstemmed Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease
title_short Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease
title_sort effects of transcranial magnetic stimulation on neurobiological changes in alzheimer's disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845030/
https://www.ncbi.nlm.nih.gov/pubmed/35119081
http://dx.doi.org/10.3892/mmr.2022.12625
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