Dachengqi Decoction Attenuates Inflammatory Response via Inhibiting HMGB1 Mediated NF-κB and P38 MAPK Signaling Pathways in Severe Acute Pancreatitis

作者
Zhuoan Chen,Yafeng Chen,Liyun Pan,Hongchang Li,Jia-min Tu,Cheng Liu,Xiuqin Dai,Xiaofen Zhang,Guifang Sun,Dian-xu Feng
出处
期刊:Cellular Physiology and Biochemistry [Karger Publishers]
卷期号:37 (4): 1379-1389 被引量:38
标识
DOI:10.1159/000430403
摘要

BACKGROUND/AIMS: Severe acute pancreatitis (SAP) is a sudden inflammation of the pancreas. The traditional Chinese medicine formula Dachengqi decoction (DCQD) is proven to be beneficial in the comprehensive treatment for pancreatitis patients in clinical practice. However, the molecular mechanism of DCQD on SAP remains unclear. High mobility group box 1(HMGB1) that functions as a damage-associated molecular pattern molecule (DAMP) has attracted much interest. METHODS: In this study, we used lipopolysaccharide (LPS) and cerulein to induce severe acute pancreatitis in C57BL/6 mice with subsequent administration with low, medium and high dose (2.3 g/kg, 7 g/kg and 21 g/kg, respectively) of DCQD. RESULTS: DCQD treatment improved the pathological score and decreased serum amylase and lipase in a dose-dependent manner. In addition, it suppressed the immune cell-induced secretion of HMGB1 and its translocation from the nucleus to the cytoplasm, thus repressing the expression of IL-6 and TNF-α. Further, pretreatment with DCQD decreased responses of TLRs, and suppressed the activation of NF-κB and p38 MAPK pathway. CONCLUSION: Decreasing the secretion of HMGB1 could reduce pro-inflammatory cytokines, which may help cutting down the risks of development from localized pathological changes to a systemic inflammatory response syndrome and even lead to multiple organ failure.
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
科勒基侈完成签到,获得积分10
1秒前
上官若男的应助被Eoch采纳,获得30
1秒前
1秒前
Ava的应助被守约采纳,获得10
2秒前
Jasper的应助被洛神之心1124采纳,获得10
2秒前
2秒前
3秒前
Allenyin发布了新的文献求助10
4秒前
4秒前
www发布了新的文献求助10
5秒前
古甘光太完成签到,获得积分10
5秒前
FashionBoy的应助被猴猴采纳,获得10
5秒前
5秒前
5秒前
5秒前
6秒前
6秒前
6秒前
6秒前
molihuakai的应助被yanyan采纳,获得10
7秒前
7秒前
SciGPT的应助被铁瓜李采纳,获得10
7秒前
8秒前
你不给你完成签到,获得积分10
8秒前
不懂学术发布了新的文献求助30
8秒前
CodeCraft的应助被Like采纳,获得10
8秒前
HY完成签到,获得积分10
8秒前
大胆妖孽发布了新的文献求助10
8秒前
9秒前
茜11122完成签到,获得积分10
9秒前
Beginner发布了新的文献求助10
9秒前
风趣纸鹤完成签到,获得积分10
10秒前
白笙发布了新的文献求助10
10秒前
蓝天的应助被YUXUAN采纳,获得10
10秒前
你不给你发布了新的文献求助10
11秒前
11秒前
大模型的应助被漆漆采纳,获得10
11秒前
11秒前
12秒前
12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
Das Matthäusevangelium: Kapitel 1:1–17 1000
IRTSD: Open-Source Data and Toolset for Electromagnetic Transient Analysis of Disturbances and IBR Control Malfunctions in Transmission Systems 1000
Comprehensive Medicinal Chemistry IV (4th Edition) 800
Entre Praga y Madrid : los contactos checoslovaco-españoles (1948-1977) 600
A REVIEW OF THE V-22 DYNAMICS VALIDATION PROGRAM 600
Les Mots du discours 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8121177
求助须知:如何正确求助?哪些是违规求助? 9525724
关于积分的说明 21557757
捐赠科研通 7699756
什么是DOI,文献DOI怎么找? 3415280
关于科研通互助平台的介绍 2541077
邀请新用户注册赠送积分活动 2455569