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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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