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The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis

Huanglian Jiedu Decoction (HJD) is used for treating sepsis in China. Active components from HJD refer to various active ingredients of HJD, while active component formulation (ACF) refers to the combination of palmatine, berberine, baicalin, and geniposide from HJD according to the quantity of HJD....

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Autores principales: Chen, Guirong, Wang, Xiaobo, Liu, Chang, Zhang, Mingbo, Han, Xueying, Xu, Yubin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500189/
https://www.ncbi.nlm.nih.gov/pubmed/36160407
http://dx.doi.org/10.3389/fphar.2022.947095
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author Chen, Guirong
Wang, Xiaobo
Liu, Chang
Zhang, Mingbo
Han, Xueying
Xu, Yubin
author_facet Chen, Guirong
Wang, Xiaobo
Liu, Chang
Zhang, Mingbo
Han, Xueying
Xu, Yubin
author_sort Chen, Guirong
collection PubMed
description Huanglian Jiedu Decoction (HJD) is used for treating sepsis in China. Active components from HJD refer to various active ingredients of HJD, while active component formulation (ACF) refers to the combination of palmatine, berberine, baicalin, and geniposide from HJD according to the quantity of HJD. The detailed mechanisms of the active components from HJD and ACF in sepsis treatment are unclear. Molecular docking, surface plasmon resonance (SPR), ELISA, RT-qPCR, and Western blotting were used to assay the possible mechanism in vitro. The efficacy and mechanism of ACF and HJD were assessed by pharmacodynamics and metabolomics analyses, respectively. The results revealed that palmatine, berberine, baicalin, and geniposide showed good binding capacity to MD-2; decreased the release of NO, TNF-α, IL-6, and IL-1β; inhibited the mRNA expression of iNOS, TNF-α, IL-6, IL-1β, and COX-2; and downregulated the protein expressions of MD-2, MyD88, p-p65, and iNOS induced by LPS; which indicated that they can inactivate the LPS-TLR4/MD-2-NF-κB pathway. Thus, ACF was formed, and the pharmacodynamics assay suggested that ACF can reduce inflammatory cell infiltration and organ damage in accordance with HJD. Furthermore, 39 metabolites were selected and identified and the regulatory effect of these metabolites by ACF and HJD was almost consistent, but ACF might alleviate physical damage caused by HJD through regulating metabolites, such as 3-hydroxyanthranilic acid. ACF could represent HJD as a new formulation to treat sepsis.
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spelling pubmed-95001892022-09-24 The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis Chen, Guirong Wang, Xiaobo Liu, Chang Zhang, Mingbo Han, Xueying Xu, Yubin Front Pharmacol Pharmacology Huanglian Jiedu Decoction (HJD) is used for treating sepsis in China. Active components from HJD refer to various active ingredients of HJD, while active component formulation (ACF) refers to the combination of palmatine, berberine, baicalin, and geniposide from HJD according to the quantity of HJD. The detailed mechanisms of the active components from HJD and ACF in sepsis treatment are unclear. Molecular docking, surface plasmon resonance (SPR), ELISA, RT-qPCR, and Western blotting were used to assay the possible mechanism in vitro. The efficacy and mechanism of ACF and HJD were assessed by pharmacodynamics and metabolomics analyses, respectively. The results revealed that palmatine, berberine, baicalin, and geniposide showed good binding capacity to MD-2; decreased the release of NO, TNF-α, IL-6, and IL-1β; inhibited the mRNA expression of iNOS, TNF-α, IL-6, IL-1β, and COX-2; and downregulated the protein expressions of MD-2, MyD88, p-p65, and iNOS induced by LPS; which indicated that they can inactivate the LPS-TLR4/MD-2-NF-κB pathway. Thus, ACF was formed, and the pharmacodynamics assay suggested that ACF can reduce inflammatory cell infiltration and organ damage in accordance with HJD. Furthermore, 39 metabolites were selected and identified and the regulatory effect of these metabolites by ACF and HJD was almost consistent, but ACF might alleviate physical damage caused by HJD through regulating metabolites, such as 3-hydroxyanthranilic acid. ACF could represent HJD as a new formulation to treat sepsis. Frontiers Media S.A. 2022-09-09 /pmc/articles/PMC9500189/ /pubmed/36160407 http://dx.doi.org/10.3389/fphar.2022.947095 Text en Copyright © 2022 Chen, Wang, Liu, Zhang, Han 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 Pharmacology
Chen, Guirong
Wang, Xiaobo
Liu, Chang
Zhang, Mingbo
Han, Xueying
Xu, Yubin
The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis
title The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis
title_full The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis
title_fullStr The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis
title_full_unstemmed The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis
title_short The interaction of MD-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis
title_sort interaction of md-2 with small molecules in huanglian jiedu decoction play a critical role in the treatment of sepsis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500189/
https://www.ncbi.nlm.nih.gov/pubmed/36160407
http://dx.doi.org/10.3389/fphar.2022.947095
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