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Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect
BACKGROUND: Sepsis is a life-threatening organ dysfunction caused by dysregulated host responses to infection, for which effective therapeutic strategies are still absent. Shengjiang San (SJS), a well-known Traditional Chinese Medicine formula, has been widely used clinically. However, its role in s...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108513/ https://www.ncbi.nlm.nih.gov/pubmed/37062835 http://dx.doi.org/10.1186/s13020-023-00744-6 |
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author | Yan, Shifan Jiang, Yu Yu, Ting Hou, Changmiao Xiao, Wen Xu, Jing Wen, Huili Wang, Jingjing Li, Shutong Chen, Fang Li, Shentang Liu, Xiehong Tan, Hao Zou, Lianhong Liu, Yanjuan Zhu, Yimin |
author_facet | Yan, Shifan Jiang, Yu Yu, Ting Hou, Changmiao Xiao, Wen Xu, Jing Wen, Huili Wang, Jingjing Li, Shutong Chen, Fang Li, Shentang Liu, Xiehong Tan, Hao Zou, Lianhong Liu, Yanjuan Zhu, Yimin |
author_sort | Yan, Shifan |
collection | PubMed |
description | BACKGROUND: Sepsis is a life-threatening organ dysfunction caused by dysregulated host responses to infection, for which effective therapeutic strategies are still absent. Shengjiang San (SJS), a well-known Traditional Chinese Medicine formula, has been widely used clinically. However, its role in sepsis-induced lung injury remains unclear. METHODS: To explore its specific mechanism, we firstly established a sepsis animal model using cecal ligation and puncture (CLP) and treated MH-S cells with LPS plus ATP. Then, UPLC/Q-TOF–MS/MS was utilized to identify its active ingredients. Network pharmacology analysis was performed to uncover the potential mechanism. HE staining and biochemical analysis were conducted to validate its therapeutic effect. ELISA was applied to detect the release of pro-inflammatory and anti-inflammatory cytokines. Western blot was utilized to detect the protein levels of GSDMD, NLRP3, P65, ASC and caspase-1. RESULTS: SJS could dramatically increase the survival rate of sepsis. In addition, it is able to inhibit the pro-inflammatory cytokines release at day 1 post CLP while promote their production at day 7, indicating SJS could attenuate uncontrolled inflammatory response in the early stage and improve immunosuppression in the late phase. Network pharmacology analysis showed that pyroptosis is the crucial action SJS exerted in the protection of sepsis-induced lung injury. Western blot data implicated SJS could attenuate pyroptosis in early sepsis while enhance in the late phase. CONCLUSIONS: SJS acted to alleviate sepsis-induced lung injury through its bidirectional regulatory effect. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-023-00744-6. |
format | Online Article Text |
id | pubmed-10108513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101085132023-04-18 Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect Yan, Shifan Jiang, Yu Yu, Ting Hou, Changmiao Xiao, Wen Xu, Jing Wen, Huili Wang, Jingjing Li, Shutong Chen, Fang Li, Shentang Liu, Xiehong Tan, Hao Zou, Lianhong Liu, Yanjuan Zhu, Yimin Chin Med Research BACKGROUND: Sepsis is a life-threatening organ dysfunction caused by dysregulated host responses to infection, for which effective therapeutic strategies are still absent. Shengjiang San (SJS), a well-known Traditional Chinese Medicine formula, has been widely used clinically. However, its role in sepsis-induced lung injury remains unclear. METHODS: To explore its specific mechanism, we firstly established a sepsis animal model using cecal ligation and puncture (CLP) and treated MH-S cells with LPS plus ATP. Then, UPLC/Q-TOF–MS/MS was utilized to identify its active ingredients. Network pharmacology analysis was performed to uncover the potential mechanism. HE staining and biochemical analysis were conducted to validate its therapeutic effect. ELISA was applied to detect the release of pro-inflammatory and anti-inflammatory cytokines. Western blot was utilized to detect the protein levels of GSDMD, NLRP3, P65, ASC and caspase-1. RESULTS: SJS could dramatically increase the survival rate of sepsis. In addition, it is able to inhibit the pro-inflammatory cytokines release at day 1 post CLP while promote their production at day 7, indicating SJS could attenuate uncontrolled inflammatory response in the early stage and improve immunosuppression in the late phase. Network pharmacology analysis showed that pyroptosis is the crucial action SJS exerted in the protection of sepsis-induced lung injury. Western blot data implicated SJS could attenuate pyroptosis in early sepsis while enhance in the late phase. CONCLUSIONS: SJS acted to alleviate sepsis-induced lung injury through its bidirectional regulatory effect. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-023-00744-6. BioMed Central 2023-04-17 /pmc/articles/PMC10108513/ /pubmed/37062835 http://dx.doi.org/10.1186/s13020-023-00744-6 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yan, Shifan Jiang, Yu Yu, Ting Hou, Changmiao Xiao, Wen Xu, Jing Wen, Huili Wang, Jingjing Li, Shutong Chen, Fang Li, Shentang Liu, Xiehong Tan, Hao Zou, Lianhong Liu, Yanjuan Zhu, Yimin Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect |
title | Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect |
title_full | Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect |
title_fullStr | Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect |
title_full_unstemmed | Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect |
title_short | Shengjiang San alleviated sepsis-induced lung injury through its bidirectional regulatory effect |
title_sort | shengjiang san alleviated sepsis-induced lung injury through its bidirectional regulatory effect |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108513/ https://www.ncbi.nlm.nih.gov/pubmed/37062835 http://dx.doi.org/10.1186/s13020-023-00744-6 |
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