A traditional herbal formula, Deng-Shi-Qing-Mai-Tang, regulates TLR4/NF-κB signaling pathway to reduce inflammatory response in PM2.5-induced lung injury

免疫印迹 医学 NF-κB 炎症 药理学 TLR4型 体内 免疫学 内科学 信号转导 传统医学 化学 生物 细胞生物学 生物化学 生物技术 基因
作者
You Zhou,Jianbo Liu,Cheng Jiang,Jiaming Chen,Xilian Feng,Weiyan Chen,Jiechun Zhang,Hongzhen Dong,Wei Zhang
出处
期刊:Phytomedicine [Elsevier BV]
卷期号:91: 153665-153665 被引量:12
标识
DOI:10.1016/j.phymed.2021.153665
摘要

Studies revealed that particulate matter 2.5 (PM2.5) enters the lung through the respiratory tract and can damage lung tissue resulting in lung injury primarily via imbalance between pro-inflammatory and anti-inflammatory responses. Moreover, TLR4/NF-κB signaling pathways are reported to play a role in PM2.5-induced inflammation and lung injury, which is closely related to the inflammatory responses. Therefore, the traditional herbal formula, Deng-Shi-Qing-Mai-Tang (DSQMT), has been applied to improve patients' clinical symptoms with lung injury induced by PM2.5. It can reduce inflammatory reactions in lung injury and relieve cough and phlegm. However, the underlying mechanism of DSQMT treatment is still exclusive. To clarify the preventive and therapeutic effects of DSQMT on PM2.5-induced lung injury and explore its underlying mechanism. PM2.5-induced lung injury rat model was established, and DSQMT was administered. First, PM2.5 was collected, and PM2.5 suspension was prepared. Then, a rat model with PM2.5-induced lung injury was established, and the effects of DSQMT were evaluated in vivo. Finally, the roles of DSQMT in inhibiting the TLR4/NF-κB signaling pathway were investigated in vitro using the NR8383 cell line via Western blot analysis, real-time PCR, electrophoretic mobility shift assay (EMSA), and immunofluorescence staining, respectively and analyzed. We found that DSQMT significantly attenuated pathological lung tissue damage and inflammatory responses in PM2.5-induced lung injury. We also found that after PM2.5 stimulation in vitro, DSQMT regulates the expression of TLR4, MyD88, IKK, IκB-α, NF-κB p65 in the TLR4/NF-κB signaling pathway. It also constrains activated NF-κB entry into the nucleus and further limits its binding to target DNA. In addition, we revealed that DSQMT down-regulated interleukin (IL)-1β, IL-6, IL-10, THF-α, NO, PGE2 to reduce the inflammatory response. We demonstrated that DSQMT has preventive and therapeutic effects on PM2.5-induced lung injury by down-regulation of the TLR4/NF-κB signaling pathway. Therefore, the efficacy of traditional Chinese medicine (TCM) in PM2.5 lung injury can be taken into consideration and may be improved in the future through further researches.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
所所应助大力出奇迹采纳,获得10
1秒前
1秒前
1秒前
风中的太阳完成签到,获得积分20
2秒前
追寻的谷冬完成签到,获得积分20
2秒前
2秒前
乐乐应助爱听歌访蕊采纳,获得10
2秒前
Ava应助niuma采纳,获得10
3秒前
4秒前
玄米茶完成签到,获得积分10
4秒前
更好的我完成签到,获得积分10
5秒前
热心市民小红花应助yagami采纳,获得10
5秒前
6秒前
6秒前
温暖书文完成签到,获得积分20
6秒前
Bihhh发布了新的文献求助10
6秒前
称心的绿柏完成签到,获得积分10
7秒前
小叶子发布了新的文献求助10
8秒前
zyw发布了新的文献求助10
8秒前
Glitter发布了新的文献求助10
8秒前
搜集达人应助震动的绿竹采纳,获得10
10秒前
10秒前
佟白易发布了新的文献求助10
10秒前
11秒前
学学术术小小白白完成签到,获得积分10
11秒前
11秒前
13秒前
哈哈完成签到,获得积分10
14秒前
xiaoqian完成签到,获得积分10
14秒前
假梦中的妍完成签到,获得积分10
14秒前
酷波er应助十二采纳,获得10
15秒前
现代曼香发布了新的文献求助10
15秒前
huyuan发布了新的文献求助10
16秒前
槿曦完成签到 ,获得积分10
17秒前
17秒前
sqqa发布了新的文献求助10
18秒前
vespa完成签到,获得积分10
18秒前
搜集达人应助狂野的微笑采纳,获得10
19秒前
芋泥蛋糕完成签到,获得积分10
19秒前
高分求助中
Applied Survey Data Analysis (第三版, 2025) 800
Assessing and Diagnosing Young Children with Neurodevelopmental Disorders (2nd Edition) 700
Images that translate 500
Algorithmic Mathematics in Machine Learning 500
Handbook of Innovations in Political Psychology 400
Mapping the Stars: Celebrity, Metonymy, and the Networked Politics of Identity 400
Nucleophilic substitution in azasydnone-modified dinitroanisoles 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3842288
求助须知:如何正确求助?哪些是违规求助? 3384399
关于积分的说明 10534504
捐赠科研通 3104830
什么是DOI,文献DOI怎么找? 1709838
邀请新用户注册赠送积分活动 823410
科研通“疑难数据库(出版商)”最低求助积分说明 774050