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A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway
Idiopathic pulmonary fibrosis (IPF) is a devastating and common chronic lung disease pathologically characterized by loss of epithelial cells and activation of fibroblasts and myofibroblasts. The etiology of IPF remains unclear and the disease pathology is poorly understood with no known efficacious...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237877/ https://www.ncbi.nlm.nih.gov/pubmed/30443024 http://dx.doi.org/10.1038/s41598-018-35320-8 |
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author | Kim, Kyung Hwa Lee, Sujin Lee, Hyunji Shin, Dasom Min, Daeun Kim, Miran Ryu, Byeol Kim, Hyeon Woo Bae, Hyunsu |
author_facet | Kim, Kyung Hwa Lee, Sujin Lee, Hyunji Shin, Dasom Min, Daeun Kim, Miran Ryu, Byeol Kim, Hyeon Woo Bae, Hyunsu |
author_sort | Kim, Kyung Hwa |
collection | PubMed |
description | Idiopathic pulmonary fibrosis (IPF) is a devastating and common chronic lung disease pathologically characterized by loss of epithelial cells and activation of fibroblasts and myofibroblasts. The etiology of IPF remains unclear and the disease pathology is poorly understood with no known efficacious therapy. PM014 is an herbal extract that has been shown to have beneficial effects in pulmonary diseases, which are likely to exert anti-inflammatory bioactions. In the present study, we observed that bleomycin (BLM) caused increased inflammatory infiltration as well as collagen deposition in lungs of mice on day 14 after treatment. Administration of PM014 suppressed BLM-induced inflammatory responses and fibrotic changes in dose-dependent manner in mice. Additionally, we provided in vitro evidence suggesting that PM014 inhibited TGF-β1-induced epithelial-mesenchymal transition (EMT) and fibroblast activation in alveolar epithelial cells and human lung fibroblasts from healthy donor and IPF patients. PM014 appeared to target TGF-β1 signaling via Smad-dependent pathways and p38 mitogen-activated protein kinases (MAPKs) pathways. Taken together, our data suggest that PM014 administration exerts a protective effect against lung fibrosis and highlight PM014 as a viable treatment option that may bring benefits to patient with IPF. |
format | Online Article Text |
id | pubmed-6237877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62378772018-11-23 A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway Kim, Kyung Hwa Lee, Sujin Lee, Hyunji Shin, Dasom Min, Daeun Kim, Miran Ryu, Byeol Kim, Hyeon Woo Bae, Hyunsu Sci Rep Article Idiopathic pulmonary fibrosis (IPF) is a devastating and common chronic lung disease pathologically characterized by loss of epithelial cells and activation of fibroblasts and myofibroblasts. The etiology of IPF remains unclear and the disease pathology is poorly understood with no known efficacious therapy. PM014 is an herbal extract that has been shown to have beneficial effects in pulmonary diseases, which are likely to exert anti-inflammatory bioactions. In the present study, we observed that bleomycin (BLM) caused increased inflammatory infiltration as well as collagen deposition in lungs of mice on day 14 after treatment. Administration of PM014 suppressed BLM-induced inflammatory responses and fibrotic changes in dose-dependent manner in mice. Additionally, we provided in vitro evidence suggesting that PM014 inhibited TGF-β1-induced epithelial-mesenchymal transition (EMT) and fibroblast activation in alveolar epithelial cells and human lung fibroblasts from healthy donor and IPF patients. PM014 appeared to target TGF-β1 signaling via Smad-dependent pathways and p38 mitogen-activated protein kinases (MAPKs) pathways. Taken together, our data suggest that PM014 administration exerts a protective effect against lung fibrosis and highlight PM014 as a viable treatment option that may bring benefits to patient with IPF. Nature Publishing Group UK 2018-11-15 /pmc/articles/PMC6237877/ /pubmed/30443024 http://dx.doi.org/10.1038/s41598-018-35320-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Kyung Hwa Lee, Sujin Lee, Hyunji Shin, Dasom Min, Daeun Kim, Miran Ryu, Byeol Kim, Hyeon Woo Bae, Hyunsu A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway |
title | A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway |
title_full | A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway |
title_fullStr | A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway |
title_full_unstemmed | A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway |
title_short | A standardized herbal extract PM014 ameliorates pulmonary fibrosis by suppressing the TGF-β1 pathway |
title_sort | standardized herbal extract pm014 ameliorates pulmonary fibrosis by suppressing the tgf-β1 pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237877/ https://www.ncbi.nlm.nih.gov/pubmed/30443024 http://dx.doi.org/10.1038/s41598-018-35320-8 |
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