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The effect of mild hypothermia plus rutin on the treatment of spinal cord injury and inflammatory factors by repressing TGF-β/smad pathway
PURPOSE: To probe the mechanism of mild hypothermia combined with rutin in the treatment of spinal cord injury (SCI). METHODS: Thirty rats were randomized into the following groups: control, sham, model, mild hypothermia (MH), and mild hypothermia plus rutin (MH+Rutin). We used modified Allen’s meth...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112105/ https://www.ncbi.nlm.nih.gov/pubmed/33978063 http://dx.doi.org/10.1590/ACB360307 |
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author | Yao, Shudan Wang, Lihang Chen, Qiling Lu, Tingsheng Pu, Xingwei Luo, Chunshan |
author_facet | Yao, Shudan Wang, Lihang Chen, Qiling Lu, Tingsheng Pu, Xingwei Luo, Chunshan |
author_sort | Yao, Shudan |
collection | PubMed |
description | PURPOSE: To probe the mechanism of mild hypothermia combined with rutin in the treatment of spinal cord injury (SCI). METHODS: Thirty rats were randomized into the following groups: control, sham, model, mild hypothermia (MH), and mild hypothermia plus rutin (MH+Rutin). We used modified Allen’s method to injure the spinal cord (T10) in rats, and then treated it with MH or/and rutin immediately. BBB scores were performed on all rats. We used HE staining for observing the injured spinal cord tissue; ELISA for assaying TNF-α, IL-1β, IL-8, Myeloperoxidase (MPO), and Malondialdehyde (MDA) contents; Dihydroethidium (DHE) for measuring the reactive oxygen species (ROS) content; flow cytometry for detecting apoptosis; and both RT-qPCR and Western blot for determining the expression levels of TGF-β/Smad pathway related proteins (TGF-β, Smad2, and Smad3). RESULTS: In comparison with model group, the BBB score of MH increased to a certain extent and MH+Rutin group increased more than MH group (p < 0.05). After treatment with MH and MH+Rutin, the inflammatory infiltration diminished. MH and MH+Rutin tellingly dwindled TNF-β, MDA and ROS contents (p < 0.01), and minified spinal cord cell apoptosis. MH and MH+Rutin could patently diminished TGF-β1, Smad2, and Smad3 expression (p < 0.01). CONCLUSIONS: MH+Rutin can suppress the activation of TGF-β/Smad pathway, hence repressing the cellular inflammatory response after SCI. |
format | Online Article Text |
id | pubmed-8112105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia |
record_format | MEDLINE/PubMed |
spelling | pubmed-81121052021-05-17 The effect of mild hypothermia plus rutin on the treatment of spinal cord injury and inflammatory factors by repressing TGF-β/smad pathway Yao, Shudan Wang, Lihang Chen, Qiling Lu, Tingsheng Pu, Xingwei Luo, Chunshan Acta Cir Bras Original Article PURPOSE: To probe the mechanism of mild hypothermia combined with rutin in the treatment of spinal cord injury (SCI). METHODS: Thirty rats were randomized into the following groups: control, sham, model, mild hypothermia (MH), and mild hypothermia plus rutin (MH+Rutin). We used modified Allen’s method to injure the spinal cord (T10) in rats, and then treated it with MH or/and rutin immediately. BBB scores were performed on all rats. We used HE staining for observing the injured spinal cord tissue; ELISA for assaying TNF-α, IL-1β, IL-8, Myeloperoxidase (MPO), and Malondialdehyde (MDA) contents; Dihydroethidium (DHE) for measuring the reactive oxygen species (ROS) content; flow cytometry for detecting apoptosis; and both RT-qPCR and Western blot for determining the expression levels of TGF-β/Smad pathway related proteins (TGF-β, Smad2, and Smad3). RESULTS: In comparison with model group, the BBB score of MH increased to a certain extent and MH+Rutin group increased more than MH group (p < 0.05). After treatment with MH and MH+Rutin, the inflammatory infiltration diminished. MH and MH+Rutin tellingly dwindled TNF-β, MDA and ROS contents (p < 0.01), and minified spinal cord cell apoptosis. MH and MH+Rutin could patently diminished TGF-β1, Smad2, and Smad3 expression (p < 0.01). CONCLUSIONS: MH+Rutin can suppress the activation of TGF-β/Smad pathway, hence repressing the cellular inflammatory response after SCI. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2021-05-07 /pmc/articles/PMC8112105/ /pubmed/33978063 http://dx.doi.org/10.1590/ACB360307 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yao, Shudan Wang, Lihang Chen, Qiling Lu, Tingsheng Pu, Xingwei Luo, Chunshan The effect of mild hypothermia plus rutin on the treatment of spinal cord injury and inflammatory factors by repressing TGF-β/smad pathway |
title | The effect of mild hypothermia plus rutin on the treatment of spinal
cord injury and inflammatory factors by repressing TGF-β/smad
pathway |
title_full | The effect of mild hypothermia plus rutin on the treatment of spinal
cord injury and inflammatory factors by repressing TGF-β/smad
pathway |
title_fullStr | The effect of mild hypothermia plus rutin on the treatment of spinal
cord injury and inflammatory factors by repressing TGF-β/smad
pathway |
title_full_unstemmed | The effect of mild hypothermia plus rutin on the treatment of spinal
cord injury and inflammatory factors by repressing TGF-β/smad
pathway |
title_short | The effect of mild hypothermia plus rutin on the treatment of spinal
cord injury and inflammatory factors by repressing TGF-β/smad
pathway |
title_sort | effect of mild hypothermia plus rutin on the treatment of spinal
cord injury and inflammatory factors by repressing tgf-β/smad
pathway |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112105/ https://www.ncbi.nlm.nih.gov/pubmed/33978063 http://dx.doi.org/10.1590/ACB360307 |
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