Cargando…

Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury

[Image: see text] Increasing evidence indicates that mitochondrial fission imbalance plays an important role in delayed neuronal cell death. Our previous study found that photobiomodulation improved the motor function of rats with spinal cord injury. However, the precise mechanism remains unclear. T...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Xin, Wang, Xuan-Kang, Zhu, Zhi-Jie, Liang, Zhuo-Wen, Li, Peng-Hui, Ma, Yang-Guang, Ding, Tan, Li, Kun, Zuo, Xiao-Shuang, Ju, Cheng, Zhang, Zhi-Hao, Song, Zhi-Wen, Quan, Hui-Lin, Zhang, Jia-Wei, Luo, Liang, Wang, Zhe, Hu, Xue-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233780/
https://www.ncbi.nlm.nih.gov/pubmed/36926726
http://dx.doi.org/10.4103/1673-5374.366491
_version_ 1785052332705185792
author Li, Xin
Wang, Xuan-Kang
Zhu, Zhi-Jie
Liang, Zhuo-Wen
Li, Peng-Hui
Ma, Yang-Guang
Ding, Tan
Li, Kun
Zuo, Xiao-Shuang
Ju, Cheng
Zhang, Zhi-Hao
Song, Zhi-Wen
Quan, Hui-Lin
Zhang, Jia-Wei
Luo, Liang
Wang, Zhe
Hu, Xue-Yu
author_facet Li, Xin
Wang, Xuan-Kang
Zhu, Zhi-Jie
Liang, Zhuo-Wen
Li, Peng-Hui
Ma, Yang-Guang
Ding, Tan
Li, Kun
Zuo, Xiao-Shuang
Ju, Cheng
Zhang, Zhi-Hao
Song, Zhi-Wen
Quan, Hui-Lin
Zhang, Jia-Wei
Luo, Liang
Wang, Zhe
Hu, Xue-Yu
author_sort Li, Xin
collection PubMed
description [Image: see text] Increasing evidence indicates that mitochondrial fission imbalance plays an important role in delayed neuronal cell death. Our previous study found that photobiomodulation improved the motor function of rats with spinal cord injury. However, the precise mechanism remains unclear. To investigate the effect of photobiomodulation on mitochondrial fission imbalance after spinal cord injury, in this study, we treated rat models of spinal cord injury with 60-minute photobiomodulation (810 nm, 150 mW) every day for 14 consecutive days. Transmission electron microscopy results confirmed the swollen and fragmented alterations of mitochondrial morphology in neurons in acute (1 day) and subacute (7 and 14 days) phases. Photobiomodulation alleviated mitochondrial fission imbalance in spinal cord tissue in the subacute phase, reduced neuronal cell death, and improved rat posterior limb motor function in a time-dependent manner. These findings suggest that photobiomodulation targets neuronal mitochondria, alleviates mitochondrial fission imbalance-induced neuronal apoptosis, and thereby promotes the motor function recovery of rats with spinal cord injury.
format Online
Article
Text
id pubmed-10233780
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-102337802023-06-02 Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury Li, Xin Wang, Xuan-Kang Zhu, Zhi-Jie Liang, Zhuo-Wen Li, Peng-Hui Ma, Yang-Guang Ding, Tan Li, Kun Zuo, Xiao-Shuang Ju, Cheng Zhang, Zhi-Hao Song, Zhi-Wen Quan, Hui-Lin Zhang, Jia-Wei Luo, Liang Wang, Zhe Hu, Xue-Yu Neural Regen Res Research Article [Image: see text] Increasing evidence indicates that mitochondrial fission imbalance plays an important role in delayed neuronal cell death. Our previous study found that photobiomodulation improved the motor function of rats with spinal cord injury. However, the precise mechanism remains unclear. To investigate the effect of photobiomodulation on mitochondrial fission imbalance after spinal cord injury, in this study, we treated rat models of spinal cord injury with 60-minute photobiomodulation (810 nm, 150 mW) every day for 14 consecutive days. Transmission electron microscopy results confirmed the swollen and fragmented alterations of mitochondrial morphology in neurons in acute (1 day) and subacute (7 and 14 days) phases. Photobiomodulation alleviated mitochondrial fission imbalance in spinal cord tissue in the subacute phase, reduced neuronal cell death, and improved rat posterior limb motor function in a time-dependent manner. These findings suggest that photobiomodulation targets neuronal mitochondria, alleviates mitochondrial fission imbalance-induced neuronal apoptosis, and thereby promotes the motor function recovery of rats with spinal cord injury. Wolters Kluwer - Medknow 2023-01-05 /pmc/articles/PMC10233780/ /pubmed/36926726 http://dx.doi.org/10.4103/1673-5374.366491 Text en Copyright: © 2023 Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons AttributionNonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Li, Xin
Wang, Xuan-Kang
Zhu, Zhi-Jie
Liang, Zhuo-Wen
Li, Peng-Hui
Ma, Yang-Guang
Ding, Tan
Li, Kun
Zuo, Xiao-Shuang
Ju, Cheng
Zhang, Zhi-Hao
Song, Zhi-Wen
Quan, Hui-Lin
Zhang, Jia-Wei
Luo, Liang
Wang, Zhe
Hu, Xue-Yu
Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury
title Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury
title_full Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury
title_fullStr Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury
title_full_unstemmed Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury
title_short Photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury
title_sort photobiomodulation provides neuroprotection through regulating mitochondrial fission imbalance in the subacute phase of spinal cord injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233780/
https://www.ncbi.nlm.nih.gov/pubmed/36926726
http://dx.doi.org/10.4103/1673-5374.366491
work_keys_str_mv AT lixin photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT wangxuankang photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT zhuzhijie photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT liangzhuowen photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT lipenghui photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT mayangguang photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT dingtan photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT likun photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT zuoxiaoshuang photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT jucheng photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT zhangzhihao photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT songzhiwen photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT quanhuilin photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT zhangjiawei photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT luoliang photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT wangzhe photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury
AT huxueyu photobiomodulationprovidesneuroprotectionthroughregulatingmitochondrialfissionimbalanceinthesubacutephaseofspinalcordinjury