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

被引:62
作者
Chen, Zhuoan [1 ]
Chen, Yafeng [2 ]
Pan, Liyun [2 ]
Li, Hongchang [2 ]
Tu, Jiamin [2 ]
Liu, Cheng [1 ]
Dai, Xiuqin [1 ]
Zhang, Xiaofen [2 ]
Sun, Guifang [2 ]
Feng, Dianxu [2 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Putuo Hosp, Lab Ctr, Shanghai, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Putuo Hosp, Dept Gen Surg, Shanghai, Peoples R China
关键词
Dachengqi decoction; Severe acute pancreatitis; HMGB1; TLRs; NF-kappa B signaling pathway; MAPK signaling pathway; TOLL-LIKE RECEPTORS; DAMPS;
D O I
10.1159/000430403
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
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 ([PS) 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-alpha. Further, pretreatment with DCQD decreased responses of TLRs, and suppressed the activation of NF-kappa B 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. (C) 2015 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:1379 / 1389
页数:11
相关论文
共 29 条
[1]
Ahrnad R, 2014, CELL PHYSIOL BIOCHEM, V34, P929
[2]
HMGB1 Is a Therapeutic Target for Sterile Inflammation and Infection [J].
Andersson, Ulf ;
Tracey, Kevin J. .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 29, 2011, 29 :139-162
[3]
Intracellular Toll-like Receptors [J].
Blasius, Amanda L. ;
Beutler, Bruce .
IMMUNITY, 2010, 32 (03) :305-315
[4]
Toll-like Receptors in Inflammatory Bowel Diseases: A Decade Later [J].
Cario, Elke .
INFLAMMATORY BOWEL DISEASES, 2010, 16 (09) :1583-1597
[5]
HMGB1 plays a critical role in vascular inflammation and lesion formation via toll-like receptor 9 [J].
Hirata, Yoichiro ;
Kurobe, Hirotsugu ;
Higashida, Mayuko ;
Fukuda, Daiju ;
Shimabukuro, Michio ;
Tanaka, Kimie ;
Higashikuni, Yasutomi ;
Kitagawa, Tetsuya ;
Sata, Masataka .
ATHEROSCLEROSIS, 2013, 231 (02) :227-233
[6]
Sterile inflammation in the liver and pancreas [J].
Hoque, Rafaz ;
Farooq, Ahmad ;
Mehal, Wajahat Z. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2013, 28 :61-67
[7]
TLR9 and the NLRP3 Inflammasome Link Acinar Cell Death With Inflammation in Acute Pancreatitis [J].
Hoque, Rafaz ;
Sohail, Muhammad ;
Malik, Ahsan ;
Sarwar, Sherhayar ;
Luo, Yuhuan ;
Shah, Ahsan ;
Barrat, Franck ;
Flavell, Richard ;
Gorelick, Fred ;
Husain, Sohail ;
Mehal, Wajahat .
GASTROENTEROLOGY, 2011, 141 (01) :358-369
[8]
High Mobility Group Box Protein 1 (HMGB1)-Partner Molecule Complexes Enhance Cytokine Production by Signaling Through the Partner Molecule Receptor [J].
Hreggvidsdottir, Hulda Sigridur ;
Lundberg, Anna M. ;
Aveberger, Ann-Charlotte ;
Klevenvall, Lena ;
Andersson, Ulf ;
Harris, Helena Erlandsson .
MOLECULAR MEDICINE, 2012, 18 (02) :224-230
[9]
The alarmin HMGB1 acts in synergy with endogenous and exogenous danger signals to promote inflammation [J].
Hreggvidsdottir, Hulda Sigridur ;
Ostberg, Therese ;
Wahamaa, Heidi ;
Schierbeck, Hanna ;
Aveberger, Ann-Charlotte ;
Klevenvall, Lena ;
Palmblad, Karin ;
Ottosson, Lars ;
Andersson, Ulf ;
Harris, Helena Erlandsson .
JOURNAL OF LEUKOCYTE BIOLOGY, 2009, 86 (03) :655-662
[10]
Huang X, 2000, WORLD J GASTROENTERO, V6, P384