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Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury

OBJECTIVES: Spinal cord injury (SCI) is a disabling central nervous system disorder. This study aimed to explore the effects of repetitive trans-spinal magnetic stimulation (rTSMS) of different spinal cord segments on movement function and growth-associated protein-43 (GAP43) and 5-hydroxytryptamine...

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Autores principales: Liu, Hao, Xiong, Deqi, Pang, Rizhao, Deng, Qian, Sun, Nianyi, Zheng, Jinqi, Liu, Jiancheng, Xiang, Wu, Chen, Zhesi, Lu, Jiachun, Wang, Wenchun, Zhang, Anren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783896/
https://www.ncbi.nlm.nih.gov/pubmed/33356694
http://dx.doi.org/10.1177/0300060520970765
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author Liu, Hao
Xiong, Deqi
Pang, Rizhao
Deng, Qian
Sun, Nianyi
Zheng, Jinqi
Liu, Jiancheng
Xiang, Wu
Chen, Zhesi
Lu, Jiachun
Wang, Wenchun
Zhang, Anren
author_facet Liu, Hao
Xiong, Deqi
Pang, Rizhao
Deng, Qian
Sun, Nianyi
Zheng, Jinqi
Liu, Jiancheng
Xiang, Wu
Chen, Zhesi
Lu, Jiachun
Wang, Wenchun
Zhang, Anren
author_sort Liu, Hao
collection PubMed
description OBJECTIVES: Spinal cord injury (SCI) is a disabling central nervous system disorder. This study aimed to explore the effects of repetitive trans-spinal magnetic stimulation (rTSMS) of different spinal cord segments on movement function and growth-associated protein-43 (GAP43) and 5-hydroxytryptamine (5-HT) expression in rats after acute SCI and to preliminarily discuss the optimal rTSMS treatment site to provide a theoretical foundation and experimental evidence for clinical application of rTSMS in SCI. METHODS: A rat T10 laminectomy SCI model produced by transient application of an aneurysm clip was used in the study. The rats were divided into group A (sham surgery), group B (acute SCI without stimulation), group C (T6 segment stimulation), group D (T10 segment stimulation), and group E (L2 segment stimulation). RESULTS: In vivo magnetic stimulation protected motor function, alleviated myelin sheath damage, decreased NgR and Nogo-A expression levels, increased GAP43 and 5-HT expression levels, and inhibited terminal deoxynucleotidyl transferase dUTP nick end labeling-positive cells and apoptosis-related protein expression in rats at 8 weeks after the surgery. CONCLUSIONS: This study suggests that rTSMS can promote GAP43 and 5-HT expression and axonal regeneration in the spinal cord, which is beneficial to motor function recovery after acute SCI.
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spelling pubmed-77838962021-01-14 Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury Liu, Hao Xiong, Deqi Pang, Rizhao Deng, Qian Sun, Nianyi Zheng, Jinqi Liu, Jiancheng Xiang, Wu Chen, Zhesi Lu, Jiachun Wang, Wenchun Zhang, Anren J Int Med Res Pre-Clinical Research Report OBJECTIVES: Spinal cord injury (SCI) is a disabling central nervous system disorder. This study aimed to explore the effects of repetitive trans-spinal magnetic stimulation (rTSMS) of different spinal cord segments on movement function and growth-associated protein-43 (GAP43) and 5-hydroxytryptamine (5-HT) expression in rats after acute SCI and to preliminarily discuss the optimal rTSMS treatment site to provide a theoretical foundation and experimental evidence for clinical application of rTSMS in SCI. METHODS: A rat T10 laminectomy SCI model produced by transient application of an aneurysm clip was used in the study. The rats were divided into group A (sham surgery), group B (acute SCI without stimulation), group C (T6 segment stimulation), group D (T10 segment stimulation), and group E (L2 segment stimulation). RESULTS: In vivo magnetic stimulation protected motor function, alleviated myelin sheath damage, decreased NgR and Nogo-A expression levels, increased GAP43 and 5-HT expression levels, and inhibited terminal deoxynucleotidyl transferase dUTP nick end labeling-positive cells and apoptosis-related protein expression in rats at 8 weeks after the surgery. CONCLUSIONS: This study suggests that rTSMS can promote GAP43 and 5-HT expression and axonal regeneration in the spinal cord, which is beneficial to motor function recovery after acute SCI. SAGE Publications 2020-12-27 /pmc/articles/PMC7783896/ /pubmed/33356694 http://dx.doi.org/10.1177/0300060520970765 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Pre-Clinical Research Report
Liu, Hao
Xiong, Deqi
Pang, Rizhao
Deng, Qian
Sun, Nianyi
Zheng, Jinqi
Liu, Jiancheng
Xiang, Wu
Chen, Zhesi
Lu, Jiachun
Wang, Wenchun
Zhang, Anren
Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury
title Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury
title_full Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury
title_fullStr Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury
title_full_unstemmed Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury
title_short Effects of repetitive magnetic stimulation on motor function and GAP43 and 5-HT expression in rats with spinal cord injury
title_sort effects of repetitive magnetic stimulation on motor function and gap43 and 5-ht expression in rats with spinal cord injury
topic Pre-Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783896/
https://www.ncbi.nlm.nih.gov/pubmed/33356694
http://dx.doi.org/10.1177/0300060520970765
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