Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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
_version_ 1782424488611151872
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
work_keys_str_mv AT cuiwanchang anonhumanprimatemodelofradiationinducedcachexia
AT bennettalexanderw anonhumanprimatemodelofradiationinducedcachexia
AT zhangpei anonhumanprimatemodelofradiationinducedcachexia
AT barrowkoryr anonhumanprimatemodelofradiationinducedcachexia
AT kearneyseanr anonhumanprimatemodelofradiationinducedcachexia
AT hankeykimg anonhumanprimatemodelofradiationinducedcachexia
AT taylorhowellcheryl anonhumanprimatemodelofradiationinducedcachexia
AT gibbsallisonm anonhumanprimatemodelofradiationinducedcachexia
AT smithcassandrap anonhumanprimatemodelofradiationinducedcachexia
AT macvittiethomasj anonhumanprimatemodelofradiationinducedcachexia
AT cuiwanchang nonhumanprimatemodelofradiationinducedcachexia
AT bennettalexanderw nonhumanprimatemodelofradiationinducedcachexia
AT zhangpei nonhumanprimatemodelofradiationinducedcachexia
AT barrowkoryr nonhumanprimatemodelofradiationinducedcachexia
AT kearneyseanr nonhumanprimatemodelofradiationinducedcachexia
AT hankeykimg nonhumanprimatemodelofradiationinducedcachexia
AT taylorhowellcheryl nonhumanprimatemodelofradiationinducedcachexia
AT gibbsallisonm nonhumanprimatemodelofradiationinducedcachexia
AT smithcassandrap nonhumanprimatemodelofradiationinducedcachexia
AT macvittiethomasj nonhumanprimatemodelofradiationinducedcachexia