Cargando…

Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model

Rheumatoid arthritis (RA) is a chronic autoimmune disease that is primarily characterized by synovial inflammation. In this study, we found that a traditional Chinese decoction, Juanbi-Tang (JBT), JBT attenuated the symptoms of collagen-induced arthritis (CIA) mice and in tumor necrosis factor trans...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Tengteng, Jia, Qingyun, Chen, Tao, Yin, Hao, Tian, Xiaoting, Lin, Xi, Liu, Yang, Zhao, Yongjian, Wang, Yongjun, Shi, Qi, Huang, Chenggang, Xu, Hao, Liang, Qianqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033619/
https://www.ncbi.nlm.nih.gov/pubmed/32116720
http://dx.doi.org/10.3389/fphar.2020.00045
_version_ 1783499709595254784
author Wang, Tengteng
Jia, Qingyun
Chen, Tao
Yin, Hao
Tian, Xiaoting
Lin, Xi
Liu, Yang
Zhao, Yongjian
Wang, Yongjun
Shi, Qi
Huang, Chenggang
Xu, Hao
Liang, Qianqian
author_facet Wang, Tengteng
Jia, Qingyun
Chen, Tao
Yin, Hao
Tian, Xiaoting
Lin, Xi
Liu, Yang
Zhao, Yongjian
Wang, Yongjun
Shi, Qi
Huang, Chenggang
Xu, Hao
Liang, Qianqian
author_sort Wang, Tengteng
collection PubMed
description Rheumatoid arthritis (RA) is a chronic autoimmune disease that is primarily characterized by synovial inflammation. In this study, we found that a traditional Chinese decoction, Juanbi-Tang (JBT), JBT attenuated the symptoms of collagen-induced arthritis (CIA) mice and in tumor necrosis factor transgenic (TNF-Tg) mice by attenuating the arthritis index and hind paw thickness. According to histopathological staining of ankle sections, JBT significantly decreased the area of inflammation and reduced bone destruction of ankle joints in both these two types of mice. Moreover, decreased tartaric acid phosphatase-positive osteoclasts were observed in the JBT group compared with those found in the control group. We also revealed that JBT suppressed monocytes and T cells as well as the production of CCL2, CCR6, and CXCR3 ligands. We next used high-performance liquid chromatography to investigate the components and pharmacological properties of this classical herbal medicine in traditional Chinese medicine. Based on network pharmacology, we performed computational prediction simulation of the potential targets of JBT, which indicated the NF-kappa B pathway as its target, which was confirmed in vitro. JBT suppressed the production of pro-inflammatory cytokines including interleukin-6 (IL-6) and IL-8, and inhibited the expression of matrix metalloproteinase 1 in fibroblast-like synoviocytes derived from RA patients (MH7A cells). Furthermore, JBT also suppressed the phosphorylation of p38, JNK, and p65 in TNF-α-treated MH7A cells. In summary, this study proved that JBT could inhibit synovial inflammation and bone destruction, possibly by blocking the phosphorylation of NF-kappa B pathway-mediated production of proinflammatory effectors.
format Online
Article
Text
id pubmed-7033619
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70336192020-02-28 Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model Wang, Tengteng Jia, Qingyun Chen, Tao Yin, Hao Tian, Xiaoting Lin, Xi Liu, Yang Zhao, Yongjian Wang, Yongjun Shi, Qi Huang, Chenggang Xu, Hao Liang, Qianqian Front Pharmacol Pharmacology Rheumatoid arthritis (RA) is a chronic autoimmune disease that is primarily characterized by synovial inflammation. In this study, we found that a traditional Chinese decoction, Juanbi-Tang (JBT), JBT attenuated the symptoms of collagen-induced arthritis (CIA) mice and in tumor necrosis factor transgenic (TNF-Tg) mice by attenuating the arthritis index and hind paw thickness. According to histopathological staining of ankle sections, JBT significantly decreased the area of inflammation and reduced bone destruction of ankle joints in both these two types of mice. Moreover, decreased tartaric acid phosphatase-positive osteoclasts were observed in the JBT group compared with those found in the control group. We also revealed that JBT suppressed monocytes and T cells as well as the production of CCL2, CCR6, and CXCR3 ligands. We next used high-performance liquid chromatography to investigate the components and pharmacological properties of this classical herbal medicine in traditional Chinese medicine. Based on network pharmacology, we performed computational prediction simulation of the potential targets of JBT, which indicated the NF-kappa B pathway as its target, which was confirmed in vitro. JBT suppressed the production of pro-inflammatory cytokines including interleukin-6 (IL-6) and IL-8, and inhibited the expression of matrix metalloproteinase 1 in fibroblast-like synoviocytes derived from RA patients (MH7A cells). Furthermore, JBT also suppressed the phosphorylation of p38, JNK, and p65 in TNF-α-treated MH7A cells. In summary, this study proved that JBT could inhibit synovial inflammation and bone destruction, possibly by blocking the phosphorylation of NF-kappa B pathway-mediated production of proinflammatory effectors. Frontiers Media S.A. 2020-02-14 /pmc/articles/PMC7033619/ /pubmed/32116720 http://dx.doi.org/10.3389/fphar.2020.00045 Text en Copyright © 2020 Wang, Jia, Chen, Yin, Tian, Lin, Liu, Zhao, Wang, Shi, Huang, Xu and Liang 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, Tengteng
Jia, Qingyun
Chen, Tao
Yin, Hao
Tian, Xiaoting
Lin, Xi
Liu, Yang
Zhao, Yongjian
Wang, Yongjun
Shi, Qi
Huang, Chenggang
Xu, Hao
Liang, Qianqian
Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model
title Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model
title_full Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model
title_fullStr Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model
title_full_unstemmed Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model
title_short Alleviation of Synovial Inflammation of Juanbi-Tang on Collagen-Induced Arthritis and TNF-Tg Mice Model
title_sort alleviation of synovial inflammation of juanbi-tang on collagen-induced arthritis and tnf-tg mice model
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033619/
https://www.ncbi.nlm.nih.gov/pubmed/32116720
http://dx.doi.org/10.3389/fphar.2020.00045
work_keys_str_mv AT wangtengteng alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT jiaqingyun alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT chentao alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT yinhao alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT tianxiaoting alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT linxi alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT liuyang alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT zhaoyongjian alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT wangyongjun alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT shiqi alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT huangchenggang alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT xuhao alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel
AT liangqianqian alleviationofsynovialinflammationofjuanbitangoncollageninducedarthritisandtnftgmicemodel