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Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice
Radiation therapy is widely used for thoracic cancers. However, it occasionally causes radiation-induced lung injuries, including pneumonitis and fibrosis. Chung-Sang-Bo-Ha-Tang (CSBHT) has been traditionally used to treat chronic pulmonary disease in Korea. PM014, a modified herbal formula derived...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359558/ https://www.ncbi.nlm.nih.gov/pubmed/28322297 http://dx.doi.org/10.1038/srep45001 |
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author | Kim, Jee-Youn Shin, Dasom Lee, Gihyun Kim, Jin-Mo Kim, Dongwook An, Yong-Min Yoo, Byung Rok Chang, Hanna Kim, Miran Cho, Jaeho Bae, Hyunsu |
author_facet | Kim, Jee-Youn Shin, Dasom Lee, Gihyun Kim, Jin-Mo Kim, Dongwook An, Yong-Min Yoo, Byung Rok Chang, Hanna Kim, Miran Cho, Jaeho Bae, Hyunsu |
author_sort | Kim, Jee-Youn |
collection | PubMed |
description | Radiation therapy is widely used for thoracic cancers. However, it occasionally causes radiation-induced lung injuries, including pneumonitis and fibrosis. Chung-Sang-Bo-Ha-Tang (CSBHT) has been traditionally used to treat chronic pulmonary disease in Korea. PM014, a modified herbal formula derived from CSBHT, contains medicinal herbs of seven species. In our previous studies, PM014 exhibited anti-inflammatory effects in a chronic obstructive pulmonary disease model. In this study, we have evaluated the effects of PM014 on radiation-induced lung inflammation. Mice in the treatment group were orally administered PM014 six times for 2 weeks. Effects of PM014 on radiation pneumonitis were evaluated based on histological findings and differential cell count in bronchoalveolar lavage fluid. PM014 treatment significantly inhibited immune cell recruitment and collagen deposition in lung tissue. Normal lung volume, evaluated by radiological analysis, in PM014-treated mice was higher compared to that in irradiated control mice. PM014-treated mice exhibited significant changes in inspiratory capacity, compliance and tissue damping and elastance. Additionally, PM014 treatment resulted in the downregulation of inflammatory cytokines, chemokines, and fibrosis-related genes and a reduction in the transforming growth factor-β1-positive cell population in lung tissue. Thus, PM014 is a potent therapeutic agent for radiation-induced lung fibrosis and inflammation. |
format | Online Article Text |
id | pubmed-5359558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53595582017-03-22 Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice Kim, Jee-Youn Shin, Dasom Lee, Gihyun Kim, Jin-Mo Kim, Dongwook An, Yong-Min Yoo, Byung Rok Chang, Hanna Kim, Miran Cho, Jaeho Bae, Hyunsu Sci Rep Article Radiation therapy is widely used for thoracic cancers. However, it occasionally causes radiation-induced lung injuries, including pneumonitis and fibrosis. Chung-Sang-Bo-Ha-Tang (CSBHT) has been traditionally used to treat chronic pulmonary disease in Korea. PM014, a modified herbal formula derived from CSBHT, contains medicinal herbs of seven species. In our previous studies, PM014 exhibited anti-inflammatory effects in a chronic obstructive pulmonary disease model. In this study, we have evaluated the effects of PM014 on radiation-induced lung inflammation. Mice in the treatment group were orally administered PM014 six times for 2 weeks. Effects of PM014 on radiation pneumonitis were evaluated based on histological findings and differential cell count in bronchoalveolar lavage fluid. PM014 treatment significantly inhibited immune cell recruitment and collagen deposition in lung tissue. Normal lung volume, evaluated by radiological analysis, in PM014-treated mice was higher compared to that in irradiated control mice. PM014-treated mice exhibited significant changes in inspiratory capacity, compliance and tissue damping and elastance. Additionally, PM014 treatment resulted in the downregulation of inflammatory cytokines, chemokines, and fibrosis-related genes and a reduction in the transforming growth factor-β1-positive cell population in lung tissue. Thus, PM014 is a potent therapeutic agent for radiation-induced lung fibrosis and inflammation. Nature Publishing Group 2017-03-21 /pmc/articles/PMC5359558/ /pubmed/28322297 http://dx.doi.org/10.1038/srep45001 Text en Copyright © 2017, The Author(s) 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 Kim, Jee-Youn Shin, Dasom Lee, Gihyun Kim, Jin-Mo Kim, Dongwook An, Yong-Min Yoo, Byung Rok Chang, Hanna Kim, Miran Cho, Jaeho Bae, Hyunsu Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice |
title | Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice |
title_full | Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice |
title_fullStr | Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice |
title_full_unstemmed | Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice |
title_short | Standardized Herbal Formula PM014 Inhibits Radiation-Induced Pulmonary Inflammation in Mice |
title_sort | standardized herbal formula pm014 inhibits radiation-induced pulmonary inflammation in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5359558/ https://www.ncbi.nlm.nih.gov/pubmed/28322297 http://dx.doi.org/10.1038/srep45001 |
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