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Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats

BACKGROUND: Jinlian Xiaodu Decoction (JXD) was reported to have anti-inflammatory and lung protection effects. This study aimed to explore the role and mechanism of JXD on bleomycin (BLM)-induced pulmonary fibrosis (PF). METHODS: The UHPLC-Q/TOF-MS system was applied to analyze JXD composition. The...

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Autores principales: Wu, Zhiqiang, He, Qin, Tao, Feibao, Ye, Xuxing, Wang, Saibin, Zhu, Yijun, Zhu, Liang, Xu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246571/
https://www.ncbi.nlm.nih.gov/pubmed/35783517
http://dx.doi.org/10.1155/2022/4206364
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author Wu, Zhiqiang
He, Qin
Tao, Feibao
Ye, Xuxing
Wang, Saibin
Zhu, Yijun
Zhu, Liang
Xu, Bin
author_facet Wu, Zhiqiang
He, Qin
Tao, Feibao
Ye, Xuxing
Wang, Saibin
Zhu, Yijun
Zhu, Liang
Xu, Bin
author_sort Wu, Zhiqiang
collection PubMed
description BACKGROUND: Jinlian Xiaodu Decoction (JXD) was reported to have anti-inflammatory and lung protection effects. This study aimed to explore the role and mechanism of JXD on bleomycin (BLM)-induced pulmonary fibrosis (PF). METHODS: The UHPLC-Q/TOF-MS system was applied to analyze JXD composition. The PF model was established by BLM intratracheal administration in Wistar rats. Subsequently, BLM-treated rats were intragastrically administered with dexamethasone (DXM, 1 g/kg/d) or JXD (3.5, 7 or 14 g/kg/d). Next, the lung coefficient was calculated; H&E, Masson, and TUNEL staining were used for lung morphological analysis and apoptosis assessment. Bronchoalveolar lavage fluid (BALF) biochemical analysis was conducted to count the inflammatory cell number. The expression of inflammatory factors mRNA in the lung tissue and BALF were measured by qRT-PCR. The content and activity of oxidative stress-related proteins were detected. The expression of PF-related, apoptosis-related, and TGF-β1 pathway-related protein were assessed by immunohistochemistry or Western blot. RESULTS: Twenty-six compounds were identified from JXD in both negative and positive ion modes. In BLM-induced rats, JXD reduced the lung coefficient and alleviated PF injury. JXD decreased inflammatory cell count and TNF-α, IL-1β, IL-6, and MCP-1 content. Meanwhile, JXD blunted BLM-induced oxidative stress and a high level of HYP. Furthermore, TUNEL analysis found that JXD inhibited cell apoptosis and increased Bcl-2/Bax ratio in BLM-induced lung. Moreover, JXD relieved the role of BLM on α-SMA, TGF-β1, collagen I, fibronectin, E-cadherin protein expression, and the phosphorylation of Smad2/3 in PF rat. CONCLUSION: This study revealed the protective effect and possible element of JXD on BLM-caused PF.
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spelling pubmed-92465712022-07-01 Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats Wu, Zhiqiang He, Qin Tao, Feibao Ye, Xuxing Wang, Saibin Zhu, Yijun Zhu, Liang Xu, Bin Evid Based Complement Alternat Med Research Article BACKGROUND: Jinlian Xiaodu Decoction (JXD) was reported to have anti-inflammatory and lung protection effects. This study aimed to explore the role and mechanism of JXD on bleomycin (BLM)-induced pulmonary fibrosis (PF). METHODS: The UHPLC-Q/TOF-MS system was applied to analyze JXD composition. The PF model was established by BLM intratracheal administration in Wistar rats. Subsequently, BLM-treated rats were intragastrically administered with dexamethasone (DXM, 1 g/kg/d) or JXD (3.5, 7 or 14 g/kg/d). Next, the lung coefficient was calculated; H&E, Masson, and TUNEL staining were used for lung morphological analysis and apoptosis assessment. Bronchoalveolar lavage fluid (BALF) biochemical analysis was conducted to count the inflammatory cell number. The expression of inflammatory factors mRNA in the lung tissue and BALF were measured by qRT-PCR. The content and activity of oxidative stress-related proteins were detected. The expression of PF-related, apoptosis-related, and TGF-β1 pathway-related protein were assessed by immunohistochemistry or Western blot. RESULTS: Twenty-six compounds were identified from JXD in both negative and positive ion modes. In BLM-induced rats, JXD reduced the lung coefficient and alleviated PF injury. JXD decreased inflammatory cell count and TNF-α, IL-1β, IL-6, and MCP-1 content. Meanwhile, JXD blunted BLM-induced oxidative stress and a high level of HYP. Furthermore, TUNEL analysis found that JXD inhibited cell apoptosis and increased Bcl-2/Bax ratio in BLM-induced lung. Moreover, JXD relieved the role of BLM on α-SMA, TGF-β1, collagen I, fibronectin, E-cadherin protein expression, and the phosphorylation of Smad2/3 in PF rat. CONCLUSION: This study revealed the protective effect and possible element of JXD on BLM-caused PF. Hindawi 2022-06-23 /pmc/articles/PMC9246571/ /pubmed/35783517 http://dx.doi.org/10.1155/2022/4206364 Text en Copyright © 2022 Zhiqiang Wu et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wu, Zhiqiang
He, Qin
Tao, Feibao
Ye, Xuxing
Wang, Saibin
Zhu, Yijun
Zhu, Liang
Xu, Bin
Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats
title Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats
title_full Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats
title_fullStr Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats
title_full_unstemmed Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats
title_short Jinlian Xiaodu Decoction Protects against Bleomycin-Induced Pulmonary Fibrosis in Rats
title_sort jinlian xiaodu decoction protects against bleomycin-induced pulmonary fibrosis in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246571/
https://www.ncbi.nlm.nih.gov/pubmed/35783517
http://dx.doi.org/10.1155/2022/4206364
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