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The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice
Hepatic fibrosis represents an important event in the progression of chronic liver injury to cirrhosis, and is characterized by excessive extracellular matrix proteins aggregation. Early fibrosis can be reversed by inhibiting hepatocyte injury, inflammation, or hepatic stellate cells activation, so...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8211319/ https://www.ncbi.nlm.nih.gov/pubmed/34149411 http://dx.doi.org/10.3389/fphar.2021.655531 |
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author | Ai, Yongqiang Shi, Wei Zuo, Xiaobin Sun, Xiaoming Chen, Yuanyuan Wang, Zhilei Li, Ruisheng Song, Xueai Dai, Wenzhang Mu, Wenqing Ding, Kaixin Li, Zhiyong Li, Qiang Xiao, Xiaohe Zhan, Xiaoyan Bai, Zhaofang |
author_facet | Ai, Yongqiang Shi, Wei Zuo, Xiaobin Sun, Xiaoming Chen, Yuanyuan Wang, Zhilei Li, Ruisheng Song, Xueai Dai, Wenzhang Mu, Wenqing Ding, Kaixin Li, Zhiyong Li, Qiang Xiao, Xiaohe Zhan, Xiaoyan Bai, Zhaofang |
author_sort | Ai, Yongqiang |
collection | PubMed |
description | Hepatic fibrosis represents an important event in the progression of chronic liver injury to cirrhosis, and is characterized by excessive extracellular matrix proteins aggregation. Early fibrosis can be reversed by inhibiting hepatocyte injury, inflammation, or hepatic stellate cells activation, so the development of antifibrotic drugs is important to reduce the incidence of hepatic cirrhosis or even hepatic carcinoma. Here we demonstrate that Schisandrol B (SolB), one of the major active constituents of traditional hepato-protective Chinese medicine, Schisandra sphenanthera, significantly protects against hepatocyte injury, while Wedelolactone (WeD) suppresses the TGF-β1/Smads signaling pathway in hepatic stellate cells (HSCs) and inflammation, the combination of the two reverses hepatic fibrosis in mice and the inhibitory effect of the combination on hepatic fibrosis is superior to that of SolB or WeD treatment alone. Combined pharmacotherapy represents a promising strategy for the prevention and treatment of liver fibrosis. |
format | Online Article Text |
id | pubmed-8211319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82113192021-06-18 The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice Ai, Yongqiang Shi, Wei Zuo, Xiaobin Sun, Xiaoming Chen, Yuanyuan Wang, Zhilei Li, Ruisheng Song, Xueai Dai, Wenzhang Mu, Wenqing Ding, Kaixin Li, Zhiyong Li, Qiang Xiao, Xiaohe Zhan, Xiaoyan Bai, Zhaofang Front Pharmacol Pharmacology Hepatic fibrosis represents an important event in the progression of chronic liver injury to cirrhosis, and is characterized by excessive extracellular matrix proteins aggregation. Early fibrosis can be reversed by inhibiting hepatocyte injury, inflammation, or hepatic stellate cells activation, so the development of antifibrotic drugs is important to reduce the incidence of hepatic cirrhosis or even hepatic carcinoma. Here we demonstrate that Schisandrol B (SolB), one of the major active constituents of traditional hepato-protective Chinese medicine, Schisandra sphenanthera, significantly protects against hepatocyte injury, while Wedelolactone (WeD) suppresses the TGF-β1/Smads signaling pathway in hepatic stellate cells (HSCs) and inflammation, the combination of the two reverses hepatic fibrosis in mice and the inhibitory effect of the combination on hepatic fibrosis is superior to that of SolB or WeD treatment alone. Combined pharmacotherapy represents a promising strategy for the prevention and treatment of liver fibrosis. Frontiers Media S.A. 2021-06-03 /pmc/articles/PMC8211319/ /pubmed/34149411 http://dx.doi.org/10.3389/fphar.2021.655531 Text en Copyright © 2021 Ai, Shi, Zuo, Sun, Chen, Wang, Li, Song, Dai, Mu, Ding, Li, Li, Xiao, Zhan and Bai. 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 Ai, Yongqiang Shi, Wei Zuo, Xiaobin Sun, Xiaoming Chen, Yuanyuan Wang, Zhilei Li, Ruisheng Song, Xueai Dai, Wenzhang Mu, Wenqing Ding, Kaixin Li, Zhiyong Li, Qiang Xiao, Xiaohe Zhan, Xiaoyan Bai, Zhaofang The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice |
title | The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice |
title_full | The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice |
title_fullStr | The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice |
title_full_unstemmed | The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice |
title_short | The Combination of Schisandrol B and Wedelolactone Synergistically Reverses Hepatic Fibrosis Via Modulating Multiple Signaling Pathways in Mice |
title_sort | combination of schisandrol b and wedelolactone synergistically reverses hepatic fibrosis via modulating multiple signaling pathways in mice |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8211319/ https://www.ncbi.nlm.nih.gov/pubmed/34149411 http://dx.doi.org/10.3389/fphar.2021.655531 |
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