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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...

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Autores principales: Kim, Kyung Hwa, Lee, Sujin, Lee, Hyunji, Shin, Dasom, Min, Daeun, Kim, Miran, Ryu, Byeol, Kim, Hyeon Woo, Bae, Hyunsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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