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Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway
Idiopathic pulmonary fibrosis is a progressive lung disease with high mortality and limited therapy that is characterized by epithelial cell damage and fibroblast activation. Ellagic acid is a natural polyphenol compound widely found in fruits and nuts that has multiple pharmacological activities. I...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072668/ https://www.ncbi.nlm.nih.gov/pubmed/33912053 http://dx.doi.org/10.3389/fphar.2021.639574 |
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author | Li, Xiaohe Huang, Kai Liu, Xiaowei Ruan, Hao Ma, Ling Liang, Jingjing Cui, Yunyao Wang, Yanhua Wu, Shuyang Li, Hailong Wei, Yuli Li, Zeping Gao, Jingjing Yang, Bo Li, Xiaoping Yang, Guang Zhou, Honggang Yang, Cheng |
author_facet | Li, Xiaohe Huang, Kai Liu, Xiaowei Ruan, Hao Ma, Ling Liang, Jingjing Cui, Yunyao Wang, Yanhua Wu, Shuyang Li, Hailong Wei, Yuli Li, Zeping Gao, Jingjing Yang, Bo Li, Xiaoping Yang, Guang Zhou, Honggang Yang, Cheng |
author_sort | Li, Xiaohe |
collection | PubMed |
description | Idiopathic pulmonary fibrosis is a progressive lung disease with high mortality and limited therapy that is characterized by epithelial cell damage and fibroblast activation. Ellagic acid is a natural polyphenol compound widely found in fruits and nuts that has multiple pharmacological activities. In this study, we explored the potential effects and mechanisms of Ellagic acid on pulmonary fibrosis in vivo and in vitro. In vivo studies showed that Ellagic acid significantly alleviated bleomycin (BLM)-induced pulmonary fibrosis in mice. In vitro experiments indicated that Ellagic acid could suppress Wnt signaling and attenuate Wnt3a-induced myofibroblast activation and the phosphorylation of Erk2 and Akt. Further studies showed that Ellagic acid could induce autophagy formation in myofibroblasts mainly by suppressing mTOR signaling and promoting apoptosis of myofibroblasts. In vivo experiments revealed that Ellagic acid significantly inhibited myofibroblast activation and promoted autophagy formation. Taken together, our results show that Ellagic acid effectively attenuates BLM-induced pulmonary fibrosis in mice by suppressing myofibroblast activation and promoting autophagy and apoptosis of myofibroblasts by inhibiting the Wnt signaling pathway. |
format | Online Article Text |
id | pubmed-8072668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80726682021-04-27 Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway Li, Xiaohe Huang, Kai Liu, Xiaowei Ruan, Hao Ma, Ling Liang, Jingjing Cui, Yunyao Wang, Yanhua Wu, Shuyang Li, Hailong Wei, Yuli Li, Zeping Gao, Jingjing Yang, Bo Li, Xiaoping Yang, Guang Zhou, Honggang Yang, Cheng Front Pharmacol Pharmacology Idiopathic pulmonary fibrosis is a progressive lung disease with high mortality and limited therapy that is characterized by epithelial cell damage and fibroblast activation. Ellagic acid is a natural polyphenol compound widely found in fruits and nuts that has multiple pharmacological activities. In this study, we explored the potential effects and mechanisms of Ellagic acid on pulmonary fibrosis in vivo and in vitro. In vivo studies showed that Ellagic acid significantly alleviated bleomycin (BLM)-induced pulmonary fibrosis in mice. In vitro experiments indicated that Ellagic acid could suppress Wnt signaling and attenuate Wnt3a-induced myofibroblast activation and the phosphorylation of Erk2 and Akt. Further studies showed that Ellagic acid could induce autophagy formation in myofibroblasts mainly by suppressing mTOR signaling and promoting apoptosis of myofibroblasts. In vivo experiments revealed that Ellagic acid significantly inhibited myofibroblast activation and promoted autophagy formation. Taken together, our results show that Ellagic acid effectively attenuates BLM-induced pulmonary fibrosis in mice by suppressing myofibroblast activation and promoting autophagy and apoptosis of myofibroblasts by inhibiting the Wnt signaling pathway. Frontiers Media S.A. 2021-04-12 /pmc/articles/PMC8072668/ /pubmed/33912053 http://dx.doi.org/10.3389/fphar.2021.639574 Text en Copyright © 2021 Li, Huang, Liu, Ruan, Ma, Liang, Cui, Wang, Wu, Li, Wei, Li, Gao, Yang, Li, Yang, Zhou and Yang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Li, Xiaohe Huang, Kai Liu, Xiaowei Ruan, Hao Ma, Ling Liang, Jingjing Cui, Yunyao Wang, Yanhua Wu, Shuyang Li, Hailong Wei, Yuli Li, Zeping Gao, Jingjing Yang, Bo Li, Xiaoping Yang, Guang Zhou, Honggang Yang, Cheng Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway |
title | Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway |
title_full | Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway |
title_fullStr | Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway |
title_full_unstemmed | Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway |
title_short | Ellagic Acid Attenuates BLM-Induced Pulmonary Fibrosis via Inhibiting Wnt Signaling Pathway |
title_sort | ellagic acid attenuates blm-induced pulmonary fibrosis via inhibiting wnt signaling pathway |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072668/ https://www.ncbi.nlm.nih.gov/pubmed/33912053 http://dx.doi.org/10.3389/fphar.2021.639574 |
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