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Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome

Corticosteroids have been proved to be ineffective for Guillain-Barré syndrome, but the mechanism remains unknown. In a rabbit model of axonal Guillain-Barré syndrome, treatment with corticosteroids significantly reduced macrophage infiltration in the spinal ventral roots and the survival rate as we...

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Autores principales: Wang, Yu-Zhong, Lv, Hui, Shi, Qi-Guang, Fan, Xu-Tao, Li, Lei, Yi Wong, Anna Hiu, Hao, Yan-Lei, Si, Chuan-Ping, Li, Cui-Lan, Yuki, Nobuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565078/
https://www.ncbi.nlm.nih.gov/pubmed/26355080
http://dx.doi.org/10.1038/srep13931
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author Wang, Yu-Zhong
Lv, Hui
Shi, Qi-Guang
Fan, Xu-Tao
Li, Lei
Yi Wong, Anna Hiu
Hao, Yan-Lei
Si, Chuan-Ping
Li, Cui-Lan
Yuki, Nobuhiro
author_facet Wang, Yu-Zhong
Lv, Hui
Shi, Qi-Guang
Fan, Xu-Tao
Li, Lei
Yi Wong, Anna Hiu
Hao, Yan-Lei
Si, Chuan-Ping
Li, Cui-Lan
Yuki, Nobuhiro
author_sort Wang, Yu-Zhong
collection PubMed
description Corticosteroids have been proved to be ineffective for Guillain-Barré syndrome, but the mechanism remains unknown. In a rabbit model of axonal Guillain-Barré syndrome, treatment with corticosteroids significantly reduced macrophage infiltration in the spinal ventral roots and the survival rate as well as clinical improvement. On 30(th) day after onset, there was significantly higher frequency of axonal degeneration in the corticosteroids-treated rabbits than saline-treated rabbits. Corticosteroids may reduce the scavengers that play a crucial role for nerve regeneration, thus delay the recovery of this disease.
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spelling pubmed-45650782015-09-15 Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome Wang, Yu-Zhong Lv, Hui Shi, Qi-Guang Fan, Xu-Tao Li, Lei Yi Wong, Anna Hiu Hao, Yan-Lei Si, Chuan-Ping Li, Cui-Lan Yuki, Nobuhiro Sci Rep Article Corticosteroids have been proved to be ineffective for Guillain-Barré syndrome, but the mechanism remains unknown. In a rabbit model of axonal Guillain-Barré syndrome, treatment with corticosteroids significantly reduced macrophage infiltration in the spinal ventral roots and the survival rate as well as clinical improvement. On 30(th) day after onset, there was significantly higher frequency of axonal degeneration in the corticosteroids-treated rabbits than saline-treated rabbits. Corticosteroids may reduce the scavengers that play a crucial role for nerve regeneration, thus delay the recovery of this disease. Nature Publishing Group 2015-09-10 /pmc/articles/PMC4565078/ /pubmed/26355080 http://dx.doi.org/10.1038/srep13931 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wang, Yu-Zhong
Lv, Hui
Shi, Qi-Guang
Fan, Xu-Tao
Li, Lei
Yi Wong, Anna Hiu
Hao, Yan-Lei
Si, Chuan-Ping
Li, Cui-Lan
Yuki, Nobuhiro
Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome
title Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome
title_full Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome
title_fullStr Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome
title_full_unstemmed Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome
title_short Action mechanism of corticosteroids to aggravate Guillain-Barré syndrome
title_sort action mechanism of corticosteroids to aggravate guillain-barré syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565078/
https://www.ncbi.nlm.nih.gov/pubmed/26355080
http://dx.doi.org/10.1038/srep13931
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