Cargando…

Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation

Acute lung injury (ALI) is a common condition, particularly in the COVID-19 pandemic, which is distinguished by sudden onset of respiratory insufficiency with tachypnea, oxygen-refractory cyanosis, reduced lung compliance and diffuse infiltration of pulmonary alveoli. It is well-established that inc...

Descripción completa

Detalles Bibliográficos
Autores principales: Tang, Shun, Liang, Yuanjing, Wang, Minmin, Lei, Jiarong, Peng, Yuhui, Tao, Qiu, Ming, Tianqi, Yang, Wenyu, Zhang, Chuantao, Guo, Jinlin, Xu, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634205/
https://www.ncbi.nlm.nih.gov/pubmed/37954597
http://dx.doi.org/10.3389/fimmu.2023.1285550
_version_ 1785132782909915136
author Tang, Shun
Liang, Yuanjing
Wang, Minmin
Lei, Jiarong
Peng, Yuhui
Tao, Qiu
Ming, Tianqi
Yang, Wenyu
Zhang, Chuantao
Guo, Jinlin
Xu, Haibo
author_facet Tang, Shun
Liang, Yuanjing
Wang, Minmin
Lei, Jiarong
Peng, Yuhui
Tao, Qiu
Ming, Tianqi
Yang, Wenyu
Zhang, Chuantao
Guo, Jinlin
Xu, Haibo
author_sort Tang, Shun
collection PubMed
description Acute lung injury (ALI) is a common condition, particularly in the COVID-19 pandemic, which is distinguished by sudden onset of respiratory insufficiency with tachypnea, oxygen-refractory cyanosis, reduced lung compliance and diffuse infiltration of pulmonary alveoli. It is well-established that increasing activity of toll-like receptor 4 (TLR4)/nuclear factor kappa-B (NF-κB) signaling axis and the NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) inflammasome activation are associated with the pathogenesis of ALI. Since ALI poses a huge challenge to human health, it is urgent to tackle this affliction with therapeutic intervention. Qinhuo Shanggan oral solution (QHSG), a traditional Chinese herbal formula, is clinically used for effective medication of various lung diseases including ALI, with the action mechanism obscure. In the present study, with the rat model of lipopolysaccharide (LPS)-induced ALI, QHSG was unveiled to ameliorate ALI by alleviating the pathological features, reversing the alteration in white blood cell profile and impeding the production of inflammatory cytokines through down-regulation of TLR4/NF-κB signaling cascade and inhibition of NLRP3 inflammasome activation. In LPS-stimulated RAW264.7 mouse macrophages, QHSG was discovered to hinder the generation of inflammatory cytokines by lessening TLR4/NF-κB signaling pathway activity and weakening NLRP3 inflammasome activation. Taken together, QHSG may resolve acute lung injury, attributed to its anti-inflammation and immunoregulation by attenuation of TLR4/NF-κB signaling cascade and inhibition of NLRP3 inflammasome activation. Our findings provide a novel insight into the action mechanism of QHSG and lay a mechanistic foundation for therapeutic intervention in acute lung injury with QHSG in clinical practice.
format Online
Article
Text
id pubmed-10634205
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-106342052023-11-10 Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation Tang, Shun Liang, Yuanjing Wang, Minmin Lei, Jiarong Peng, Yuhui Tao, Qiu Ming, Tianqi Yang, Wenyu Zhang, Chuantao Guo, Jinlin Xu, Haibo Front Immunol Immunology Acute lung injury (ALI) is a common condition, particularly in the COVID-19 pandemic, which is distinguished by sudden onset of respiratory insufficiency with tachypnea, oxygen-refractory cyanosis, reduced lung compliance and diffuse infiltration of pulmonary alveoli. It is well-established that increasing activity of toll-like receptor 4 (TLR4)/nuclear factor kappa-B (NF-κB) signaling axis and the NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) inflammasome activation are associated with the pathogenesis of ALI. Since ALI poses a huge challenge to human health, it is urgent to tackle this affliction with therapeutic intervention. Qinhuo Shanggan oral solution (QHSG), a traditional Chinese herbal formula, is clinically used for effective medication of various lung diseases including ALI, with the action mechanism obscure. In the present study, with the rat model of lipopolysaccharide (LPS)-induced ALI, QHSG was unveiled to ameliorate ALI by alleviating the pathological features, reversing the alteration in white blood cell profile and impeding the production of inflammatory cytokines through down-regulation of TLR4/NF-κB signaling cascade and inhibition of NLRP3 inflammasome activation. In LPS-stimulated RAW264.7 mouse macrophages, QHSG was discovered to hinder the generation of inflammatory cytokines by lessening TLR4/NF-κB signaling pathway activity and weakening NLRP3 inflammasome activation. Taken together, QHSG may resolve acute lung injury, attributed to its anti-inflammation and immunoregulation by attenuation of TLR4/NF-κB signaling cascade and inhibition of NLRP3 inflammasome activation. Our findings provide a novel insight into the action mechanism of QHSG and lay a mechanistic foundation for therapeutic intervention in acute lung injury with QHSG in clinical practice. Frontiers Media S.A. 2023-10-25 /pmc/articles/PMC10634205/ /pubmed/37954597 http://dx.doi.org/10.3389/fimmu.2023.1285550 Text en Copyright © 2023 Tang, Liang, Wang, Lei, Peng, Tao, Ming, Yang, Zhang, Guo and Xu 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 Immunology
Tang, Shun
Liang, Yuanjing
Wang, Minmin
Lei, Jiarong
Peng, Yuhui
Tao, Qiu
Ming, Tianqi
Yang, Wenyu
Zhang, Chuantao
Guo, Jinlin
Xu, Haibo
Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation
title Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation
title_full Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation
title_fullStr Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation
title_full_unstemmed Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation
title_short Qinhuo Shanggan oral solution resolves acute lung injury by down-regulating TLR4/NF-κB signaling cascade and inhibiting NLRP3 inflammasome activation
title_sort qinhuo shanggan oral solution resolves acute lung injury by down-regulating tlr4/nf-κb signaling cascade and inhibiting nlrp3 inflammasome activation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634205/
https://www.ncbi.nlm.nih.gov/pubmed/37954597
http://dx.doi.org/10.3389/fimmu.2023.1285550
work_keys_str_mv AT tangshun qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT liangyuanjing qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT wangminmin qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT leijiarong qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT pengyuhui qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT taoqiu qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT mingtianqi qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT yangwenyu qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT zhangchuantao qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT guojinlin qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation
AT xuhaibo qinhuoshangganoralsolutionresolvesacutelunginjurybydownregulatingtlr4nfkbsignalingcascadeandinhibitingnlrp3inflammasomeactivation