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:16
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
无极微光应助逍风采纳,获得20
3秒前
开心聪展完成签到,获得积分10
4秒前
林间清晨发布了新的文献求助10
4秒前
5秒前
KK发布了新的文献求助10
5秒前
茂茂完成签到,获得积分10
6秒前
可靠寒云完成签到,获得积分10
7秒前
李健应助hai采纳,获得10
9秒前
9秒前
10秒前
10秒前
sxl完成签到 ,获得积分10
11秒前
11秒前
现实的访云完成签到,获得积分20
12秒前
12秒前
14秒前
baifeng发布了新的文献求助10
14秒前
14秒前
14秒前
14秒前
14秒前
打打应助科研通管家采纳,获得10
14秒前
赘婿应助科研通管家采纳,获得10
14秒前
Licy完成签到,获得积分10
14秒前
彭于晏应助科研通管家采纳,获得10
14秒前
段醒醒应助科研通管家采纳,获得50
14秒前
li发布了新的文献求助10
16秒前
OTON完成签到,获得积分10
16秒前
li发布了新的文献求助10
16秒前
海蓝鲸发布了新的文献求助10
17秒前
ephore应助眼花老头采纳,获得30
19秒前
19秒前
领导范儿应助睡不醒的喵采纳,获得10
19秒前
hai完成签到,获得积分10
20秒前
科研通AI6.2应助cxtz采纳,获得10
20秒前
zeyuan发布了新的文献求助10
20秒前
21秒前
molihuakai应助聋虾采纳,获得10
21秒前
22秒前
盐咸小狗完成签到 ,获得积分10
23秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
晶种分解过程与铝酸钠溶液混合强度关系的探讨 8888
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
The formation of Australian attitudes towards China, 1918-1941 640
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6430078
求助须知:如何正确求助?哪些是违规求助? 8246219
关于积分的说明 17536117
捐赠科研通 5486331
什么是DOI,文献DOI怎么找? 2895775
邀请新用户注册赠送积分活动 1872180
关于科研通互助平台的介绍 1711698