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Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis

Sepsis is a systemic inflammatory reaction caused by various infectious or noninfectious factors, which can lead to shock, multiple organ dysfunction syndrome, and death. It is one of the common complications and a main cause of death in critically ill patients. At present, the treatments of sepsis...

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Autores principales: Wu, Qi-, Yin, Chuan-hui, Li, Yi, Cai, Jie-qi, Yang, Han-yun, Huang, Ying-ying, Zheng, Yi-xu, Xiong, Ke, Yu, Hai-lang, Lu, Ai-ping, Wang, Ke-xin, Guan, Dao-gang, Chen, Yu-peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687625/
https://www.ncbi.nlm.nih.gov/pubmed/34938184
http://dx.doi.org/10.3389/fphar.2021.769190
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author Wu, Qi-
Yin, Chuan-hui
Li, Yi
Cai, Jie-qi
Yang, Han-yun
Huang, Ying-ying
Zheng, Yi-xu
Xiong, Ke
Yu, Hai-lang
Lu, Ai-ping
Wang, Ke-xin
Guan, Dao-gang
Chen, Yu-peng
author_facet Wu, Qi-
Yin, Chuan-hui
Li, Yi
Cai, Jie-qi
Yang, Han-yun
Huang, Ying-ying
Zheng, Yi-xu
Xiong, Ke
Yu, Hai-lang
Lu, Ai-ping
Wang, Ke-xin
Guan, Dao-gang
Chen, Yu-peng
author_sort Wu, Qi-
collection PubMed
description Sepsis is a systemic inflammatory reaction caused by various infectious or noninfectious factors, which can lead to shock, multiple organ dysfunction syndrome, and death. It is one of the common complications and a main cause of death in critically ill patients. At present, the treatments of sepsis are mainly focused on the controlling of inflammatory response and reduction of various organ function damage, including anti-infection, hormones, mechanical ventilation, nutritional support, and traditional Chinese medicine (TCM). Among them, Xuebijing injection (XBJI) is an important derivative of TCM, which is widely used in clinical research. However, the molecular mechanism of XBJI on sepsis is still not clear. The mechanism of treatment of “bacteria, poison and inflammation” and the effects of multi-ingredient, multi-target, and multi-pathway have still not been clarified. For solving this issue, we designed a new systems pharmacology strategy which combines target genes of XBJI and the pathogenetic genes of sepsis to construct functional response space (FRS). The key response proteins in the FRS were determined by using a novel node importance calculation method and were condensed by a dynamic programming strategy to conduct the critical functional ingredients group (CFIG). The results showed that enriched pathways of key response proteins selected from FRS could cover 95.83% of the enriched pathways of reference targets, which were defined as the intersections of ingredient targets and pathogenetic genes. The targets of the optimized CFIG with 60 ingredients could be enriched into 182 pathways which covered 81.58% of 152 pathways of 1,606 pathogenetic genes. The prediction of CFIG targets showed that the CFIG of XBJI could affect sepsis synergistically through genes such as TAK1, TNF-α, IL-1β, and MEK1 in the pathways of MAPK, NF-κB, PI3K-AKT, Toll-like receptor, and tumor necrosis factor signaling. Finally, the effects of apigenin, baicalein, and luteolin were evaluated by in vitro experiments and were proved to be effective in reducing the production of intracellular reactive oxygen species in lipopolysaccharide-stimulated RAW264.7 cells, significantly. These results indicate that the novel integrative model can promote reliability and accuracy on depicting the CFIGs in XBJI and figure out a methodological coordinate for simplicity, mechanism analysis, and secondary development of formulas in TCM.
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spelling pubmed-86876252021-12-21 Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis Wu, Qi- Yin, Chuan-hui Li, Yi Cai, Jie-qi Yang, Han-yun Huang, Ying-ying Zheng, Yi-xu Xiong, Ke Yu, Hai-lang Lu, Ai-ping Wang, Ke-xin Guan, Dao-gang Chen, Yu-peng Front Pharmacol Pharmacology Sepsis is a systemic inflammatory reaction caused by various infectious or noninfectious factors, which can lead to shock, multiple organ dysfunction syndrome, and death. It is one of the common complications and a main cause of death in critically ill patients. At present, the treatments of sepsis are mainly focused on the controlling of inflammatory response and reduction of various organ function damage, including anti-infection, hormones, mechanical ventilation, nutritional support, and traditional Chinese medicine (TCM). Among them, Xuebijing injection (XBJI) is an important derivative of TCM, which is widely used in clinical research. However, the molecular mechanism of XBJI on sepsis is still not clear. The mechanism of treatment of “bacteria, poison and inflammation” and the effects of multi-ingredient, multi-target, and multi-pathway have still not been clarified. For solving this issue, we designed a new systems pharmacology strategy which combines target genes of XBJI and the pathogenetic genes of sepsis to construct functional response space (FRS). The key response proteins in the FRS were determined by using a novel node importance calculation method and were condensed by a dynamic programming strategy to conduct the critical functional ingredients group (CFIG). The results showed that enriched pathways of key response proteins selected from FRS could cover 95.83% of the enriched pathways of reference targets, which were defined as the intersections of ingredient targets and pathogenetic genes. The targets of the optimized CFIG with 60 ingredients could be enriched into 182 pathways which covered 81.58% of 152 pathways of 1,606 pathogenetic genes. The prediction of CFIG targets showed that the CFIG of XBJI could affect sepsis synergistically through genes such as TAK1, TNF-α, IL-1β, and MEK1 in the pathways of MAPK, NF-κB, PI3K-AKT, Toll-like receptor, and tumor necrosis factor signaling. Finally, the effects of apigenin, baicalein, and luteolin were evaluated by in vitro experiments and were proved to be effective in reducing the production of intracellular reactive oxygen species in lipopolysaccharide-stimulated RAW264.7 cells, significantly. These results indicate that the novel integrative model can promote reliability and accuracy on depicting the CFIGs in XBJI and figure out a methodological coordinate for simplicity, mechanism analysis, and secondary development of formulas in TCM. Frontiers Media S.A. 2021-12-06 /pmc/articles/PMC8687625/ /pubmed/34938184 http://dx.doi.org/10.3389/fphar.2021.769190 Text en Copyright © 2021 Wu, Yin, Li, Cai, Yang, Huang, Zheng, Xiong, Yu, Lu, Wang, Guan and Chen. 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
Wu, Qi-
Yin, Chuan-hui
Li, Yi
Cai, Jie-qi
Yang, Han-yun
Huang, Ying-ying
Zheng, Yi-xu
Xiong, Ke
Yu, Hai-lang
Lu, Ai-ping
Wang, Ke-xin
Guan, Dao-gang
Chen, Yu-peng
Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis
title Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis
title_full Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis
title_fullStr Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis
title_full_unstemmed Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis
title_short Detecting Critical Functional Ingredients Group and Mechanism of Xuebijing Injection in Treating Sepsis
title_sort detecting critical functional ingredients group and mechanism of xuebijing injection in treating sepsis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687625/
https://www.ncbi.nlm.nih.gov/pubmed/34938184
http://dx.doi.org/10.3389/fphar.2021.769190
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