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An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model

BACKGROUND: Animal models suitable for investigating mechanisms behind radiation-induced muscle injury are lacking. We developed a tree shrew model of such injury and investigated pathological changes and mechanisms. METHODS: Animals were divided into control (n = 5), radiation-induced acute injury...

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Autores principales: Zhao, Pengcheng, Xia, Wei, Wei, Jianglian, Feng, Yiwei, Xie, Mao, Niu, Zhijie, Liu, Heng, Ke, Shenghui, Liu, Huayu, Tang, Anzhou, He, Guangyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961377/
https://www.ncbi.nlm.nih.gov/pubmed/35360454
http://dx.doi.org/10.1177/15593258221082878
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author Zhao, Pengcheng
Xia, Wei
Wei, Jianglian
Feng, Yiwei
Xie, Mao
Niu, Zhijie
Liu, Heng
Ke, Shenghui
Liu, Huayu
Tang, Anzhou
He, Guangyao
author_facet Zhao, Pengcheng
Xia, Wei
Wei, Jianglian
Feng, Yiwei
Xie, Mao
Niu, Zhijie
Liu, Heng
Ke, Shenghui
Liu, Huayu
Tang, Anzhou
He, Guangyao
author_sort Zhao, Pengcheng
collection PubMed
description BACKGROUND: Animal models suitable for investigating mechanisms behind radiation-induced muscle injury are lacking. We developed a tree shrew model of such injury and investigated pathological changes and mechanisms. METHODS: Animals were divided into control (n = 5), radiation-induced acute injury (n = 5), and radiation-induced chronic injury (n = 5) groups. Tensor veli palatini (TVP) muscles of acute injury and chronic injury groups were dissected under a microscope at 1 and 24 weeks after radiation therapy, respectively. TVP muscles were stained with HE and Masson to visualize pathological changes. ELISA was performed to measure oxidative injury. RT-qPCR and immunohistochemical staining was performed to measure expression levels of miR-206 and histone deacetylase 4 (HDAC4). RESULTS: Compared to the control group, acute injury group showed a significant decrease in miR-206 expression (.061 ± .38, P < .05) and a significant increase in HDAC4 expression (37.05 ± 20.68, P < .05). Chronic injury group showed a significant decrease in miR-206 expression (.23 ± .19, P < .05) and a significant increase in HDAC4 expression (9.66 ± 6.12, P < .05). DISCUSSION: A tree shrew model of radiation-induced muscle injury was established by exposing TVP muscle region to radiation of 20-Gy. Experimental results indicated that injury caused by radiation persisted despite gradual healing of the TVP muscle and miR-206 regulatory pathway plays a key role in regulating radiation-induced muscle injury.
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spelling pubmed-89613772022-03-30 An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model Zhao, Pengcheng Xia, Wei Wei, Jianglian Feng, Yiwei Xie, Mao Niu, Zhijie Liu, Heng Ke, Shenghui Liu, Huayu Tang, Anzhou He, Guangyao Dose Response Original Article BACKGROUND: Animal models suitable for investigating mechanisms behind radiation-induced muscle injury are lacking. We developed a tree shrew model of such injury and investigated pathological changes and mechanisms. METHODS: Animals were divided into control (n = 5), radiation-induced acute injury (n = 5), and radiation-induced chronic injury (n = 5) groups. Tensor veli palatini (TVP) muscles of acute injury and chronic injury groups were dissected under a microscope at 1 and 24 weeks after radiation therapy, respectively. TVP muscles were stained with HE and Masson to visualize pathological changes. ELISA was performed to measure oxidative injury. RT-qPCR and immunohistochemical staining was performed to measure expression levels of miR-206 and histone deacetylase 4 (HDAC4). RESULTS: Compared to the control group, acute injury group showed a significant decrease in miR-206 expression (.061 ± .38, P < .05) and a significant increase in HDAC4 expression (37.05 ± 20.68, P < .05). Chronic injury group showed a significant decrease in miR-206 expression (.23 ± .19, P < .05) and a significant increase in HDAC4 expression (9.66 ± 6.12, P < .05). DISCUSSION: A tree shrew model of radiation-induced muscle injury was established by exposing TVP muscle region to radiation of 20-Gy. Experimental results indicated that injury caused by radiation persisted despite gradual healing of the TVP muscle and miR-206 regulatory pathway plays a key role in regulating radiation-induced muscle injury. SAGE Publications 2022-03-26 /pmc/articles/PMC8961377/ /pubmed/35360454 http://dx.doi.org/10.1177/15593258221082878 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/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 Original Article
Zhao, Pengcheng
Xia, Wei
Wei, Jianglian
Feng, Yiwei
Xie, Mao
Niu, Zhijie
Liu, Heng
Ke, Shenghui
Liu, Huayu
Tang, Anzhou
He, Guangyao
An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model
title An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model
title_full An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model
title_fullStr An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model
title_full_unstemmed An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model
title_short An Investigation of the Mechanisms of Radiation-Induced Muscle Injury in a Tree Shrew (Tupaia belangeri) Model
title_sort investigation of the mechanisms of radiation-induced muscle injury in a tree shrew (tupaia belangeri) model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961377/
https://www.ncbi.nlm.nih.gov/pubmed/35360454
http://dx.doi.org/10.1177/15593258221082878
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