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A non-human primate model of radiation-induced cachexia
Cachexia, or muscle wasting, is a serious health threat to victims of radiological accidents or patients receiving radiotherapy. Here, we propose a non-human primate (NHP) radiation-induced cachexia model based on clinical and molecular pathology findings. NHP exposed to potentially lethal partial-b...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814846/ https://www.ncbi.nlm.nih.gov/pubmed/27029502 http://dx.doi.org/10.1038/srep23612 |
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author | Cui, Wanchang Bennett, Alexander W. Zhang, Pei Barrow, Kory R. Kearney, Sean R. Hankey, Kim G. Taylor-Howell, Cheryl Gibbs, Allison M. Smith, Cassandra P. MacVittie, Thomas J. |
author_facet | Cui, Wanchang Bennett, Alexander W. Zhang, Pei Barrow, Kory R. Kearney, Sean R. Hankey, Kim G. Taylor-Howell, Cheryl Gibbs, Allison M. Smith, Cassandra P. MacVittie, Thomas J. |
author_sort | Cui, Wanchang |
collection | PubMed |
description | Cachexia, or muscle wasting, is a serious health threat to victims of radiological accidents or patients receiving radiotherapy. Here, we propose a non-human primate (NHP) radiation-induced cachexia model based on clinical and molecular pathology findings. NHP exposed to potentially lethal partial-body irradiation developed symptoms of cachexia such as body weight loss in a time- and dose-dependent manner. Severe body weight loss as high as 20–25% was observed which was refractory to nutritional intervention. Radiographic imaging indicated that cachectic NHP lost as much as 50% of skeletal muscle. Histological analysis of muscle tissues showed abnormalities such as presence of central nuclei, inflammation, fatty replacement of skeletal muscle, and muscle fiber degeneration. Biochemical parameters such as hemoglobin and albumin levels decreased after radiation exposure. Levels of FBXO32 (Atrogin-1), ActRIIB and myostatin were significantly changed in the irradiated cachectic NHP compared to the non-irradiated NHP. Our data suggest NHP that have been exposed to high dose radiation manifest cachexia-like symptoms in a time- and dose-dependent manner. This model provides a unique opportunity to study the mechanism of radiation-induced cachexia and will aid in efficacy studies of mitigators of this disease. |
format | Online Article Text |
id | pubmed-4814846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48148462016-04-04 A non-human primate model of radiation-induced cachexia Cui, Wanchang Bennett, Alexander W. Zhang, Pei Barrow, Kory R. Kearney, Sean R. Hankey, Kim G. Taylor-Howell, Cheryl Gibbs, Allison M. Smith, Cassandra P. MacVittie, Thomas J. Sci Rep Article Cachexia, or muscle wasting, is a serious health threat to victims of radiological accidents or patients receiving radiotherapy. Here, we propose a non-human primate (NHP) radiation-induced cachexia model based on clinical and molecular pathology findings. NHP exposed to potentially lethal partial-body irradiation developed symptoms of cachexia such as body weight loss in a time- and dose-dependent manner. Severe body weight loss as high as 20–25% was observed which was refractory to nutritional intervention. Radiographic imaging indicated that cachectic NHP lost as much as 50% of skeletal muscle. Histological analysis of muscle tissues showed abnormalities such as presence of central nuclei, inflammation, fatty replacement of skeletal muscle, and muscle fiber degeneration. Biochemical parameters such as hemoglobin and albumin levels decreased after radiation exposure. Levels of FBXO32 (Atrogin-1), ActRIIB and myostatin were significantly changed in the irradiated cachectic NHP compared to the non-irradiated NHP. Our data suggest NHP that have been exposed to high dose radiation manifest cachexia-like symptoms in a time- and dose-dependent manner. This model provides a unique opportunity to study the mechanism of radiation-induced cachexia and will aid in efficacy studies of mitigators of this disease. Nature Publishing Group 2016-03-31 /pmc/articles/PMC4814846/ /pubmed/27029502 http://dx.doi.org/10.1038/srep23612 Text en Copyright © 2016, 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 Cui, Wanchang Bennett, Alexander W. Zhang, Pei Barrow, Kory R. Kearney, Sean R. Hankey, Kim G. Taylor-Howell, Cheryl Gibbs, Allison M. Smith, Cassandra P. MacVittie, Thomas J. A non-human primate model of radiation-induced cachexia |
title | A non-human primate model of radiation-induced cachexia |
title_full | A non-human primate model of radiation-induced cachexia |
title_fullStr | A non-human primate model of radiation-induced cachexia |
title_full_unstemmed | A non-human primate model of radiation-induced cachexia |
title_short | A non-human primate model of radiation-induced cachexia |
title_sort | non-human primate model of radiation-induced cachexia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814846/ https://www.ncbi.nlm.nih.gov/pubmed/27029502 http://dx.doi.org/10.1038/srep23612 |
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