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Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway
The nuclear factor (NF)-κB signaling pathway plays an important role in the initialization and development phase of inflammatory injuries, including inflammatory bowel disease (IBD). Sishen Wan (SSW) is a classic Chinese patent medicine listed in the Chinese Pharmacopoeia, which is usually used to t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414459/ https://www.ncbi.nlm.nih.gov/pubmed/30894816 http://dx.doi.org/10.3389/fphar.2019.00170 |
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author | Wang, Hai-Yan Zhao, Hai-Mei Wang, Yao Liu, Yi Lu, Xiu-Yun Liu, Xue-Ke Chen, Fang Ge, Wei Zuo, Zheng-Yun Liu, Duan-Yong |
author_facet | Wang, Hai-Yan Zhao, Hai-Mei Wang, Yao Liu, Yi Lu, Xiu-Yun Liu, Xue-Ke Chen, Fang Ge, Wei Zuo, Zheng-Yun Liu, Duan-Yong |
author_sort | Wang, Hai-Yan |
collection | PubMed |
description | The nuclear factor (NF)-κB signaling pathway plays an important role in the initialization and development phase of inflammatory injuries, including inflammatory bowel disease (IBD). Sishen Wan (SSW) is a classic Chinese patent medicine listed in the Chinese Pharmacopoeia, which is usually used to treat chronic colitis; however, it is unclear whether SSW can treat IBD via the NF-κB signaling pathway. In the present study, the therapeutic effect of SSW was demonstrated by the decreased index of colonic weight, macroscopic and microscopic score, and pathological observation in chronic colitis induced by trinitrobenzene sulfonic acid. In colonic mucosa of rats with chronic colitis, SSW reduced the levels of calprotectin and eliminated oxidative lesions; downregulated expression of interferon-γ, interleukin (IL)-1β and IL-17; increased expression of IL-4; and suppressed expression of NF-κB p65, and NF-κB essential modulator (NEMO)-like kinase (NLK). Furthermore, SSW inhibited ubiquitinated NEMO, ubiquitin-activated enzyme, and E2i activation, and phosphorylation of downstream proteins (cylindromatosis protein, transforming growth factor-β-activated kinase and P38). These results show that the therapeutic effects of SSW in chronic colitis were mediated by inhibiting the NEMO/NLK signaling pathway to suppress NF-κB activation. |
format | Online Article Text |
id | pubmed-6414459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64144592019-03-20 Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway Wang, Hai-Yan Zhao, Hai-Mei Wang, Yao Liu, Yi Lu, Xiu-Yun Liu, Xue-Ke Chen, Fang Ge, Wei Zuo, Zheng-Yun Liu, Duan-Yong Front Pharmacol Pharmacology The nuclear factor (NF)-κB signaling pathway plays an important role in the initialization and development phase of inflammatory injuries, including inflammatory bowel disease (IBD). Sishen Wan (SSW) is a classic Chinese patent medicine listed in the Chinese Pharmacopoeia, which is usually used to treat chronic colitis; however, it is unclear whether SSW can treat IBD via the NF-κB signaling pathway. In the present study, the therapeutic effect of SSW was demonstrated by the decreased index of colonic weight, macroscopic and microscopic score, and pathological observation in chronic colitis induced by trinitrobenzene sulfonic acid. In colonic mucosa of rats with chronic colitis, SSW reduced the levels of calprotectin and eliminated oxidative lesions; downregulated expression of interferon-γ, interleukin (IL)-1β and IL-17; increased expression of IL-4; and suppressed expression of NF-κB p65, and NF-κB essential modulator (NEMO)-like kinase (NLK). Furthermore, SSW inhibited ubiquitinated NEMO, ubiquitin-activated enzyme, and E2i activation, and phosphorylation of downstream proteins (cylindromatosis protein, transforming growth factor-β-activated kinase and P38). These results show that the therapeutic effects of SSW in chronic colitis were mediated by inhibiting the NEMO/NLK signaling pathway to suppress NF-κB activation. Frontiers Media S.A. 2019-03-06 /pmc/articles/PMC6414459/ /pubmed/30894816 http://dx.doi.org/10.3389/fphar.2019.00170 Text en Copyright © 2019 Wang, Zhao, Wang, Liu, Lu, Liu, Chen, Ge, Zuo and Liu. http://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 Wang, Hai-Yan Zhao, Hai-Mei Wang, Yao Liu, Yi Lu, Xiu-Yun Liu, Xue-Ke Chen, Fang Ge, Wei Zuo, Zheng-Yun Liu, Duan-Yong Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway |
title | Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway |
title_full | Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway |
title_fullStr | Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway |
title_full_unstemmed | Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway |
title_short | Sishen Wan(®) Ameliorated Trinitrobenzene-Sulfonic-Acid-Induced Chronic Colitis via NEMO/NLK Signaling Pathway |
title_sort | sishen wan(®) ameliorated trinitrobenzene-sulfonic-acid-induced chronic colitis via nemo/nlk signaling pathway |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414459/ https://www.ncbi.nlm.nih.gov/pubmed/30894816 http://dx.doi.org/10.3389/fphar.2019.00170 |
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