Hexahydrocurcumin from Zingiberis rhizoma attenuates lipopolysaccharide-induced acute pneumonia through JAK1/STAT3 signaling pathway

被引:7
作者
Li, Ruopeng [1 ,2 ]
Liang, Qinghe [1 ,2 ]
Yang, Qin [1 ,2 ]
Dai, Wenqi [1 ,2 ]
Xiao, Yao [3 ]
Pan, Hudan [3 ]
Zhang, Zhongde [3 ]
Liu, Liang [3 ]
Li, Xiaojuan [1 ,2 ]
机构
[1] Southern Med Univ, Sch Pharmaceut Sci, Innovat Program Drug Res Inflammat & Immune Dis, Lab Antiinflammat & Immunomodulat Pharmacol,NMPA K, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Screening, Guangzhou 510515, Peoples R China
[3] Guangzhou Univ Chinese Med, Affiliated Hosp 2, State Key Lab Dampness Syndrome Chinese Med, Guangzhou, Peoples R China
关键词
Hexahydrocurcumin; Pneumonia; Inflammation; JAK1; STAT3; ACUTE LUNG INJURY; NF-KAPPA-B; INFLAMMATORY RESPONSE; ACTIVATION; MECHANISMS; INHIBITORS; DISCOVERY; APOPTOSIS; THERAPY; CELLS;
D O I
10.1016/j.phymed.2023.155141
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Pneumonia is one of the major causes of death after pathogens infection. Zingiberis rhizoma (GAN JIANG) is a herb that used in combination with other Chinese medicines to treat pathogen such as virus induced pneumonia. However, the affect of hexahydrocurcumin (HHC), a component from Zingiberis rhizoma, on pneumonia remains unknown. Purpose: This study aims to explore the effects of HHC on lipopolysaccharide (LPS)-induced acute pneumonia, and to clarify the underlying mechanism. Methods: The pneumonia model of C57BL/6 mice was established by intratracheal injection of LPS to evaluate the therapeutic effect of HHC on lung injury and inflammation in vivo. RAW264.7 macrophages were utilized to illustrate the cellular mechanism of HHC in vitro. Results: HHC alleviated lung injury, ROS and inflammatory cytokine IL-6 production in pneumonia mice in vivo. Molecular docking results disclosed the binding of HHC to JAK1 protein. The study further showed that HHC suppressed the inflammatory cytokines such as IL-6, TNF-alpha, IL-1 beta gene expression, inhibited the phosphorylation of JAK1 but not JAK3, and the subsequent STAT3 phosphorylation in LPS-activated macrophages. HHC exhibited no effects on the protein levels of JAK1 and STAT3 in vitro. Consistently, HHC also attenuated the JAK1, STAT3 phosphorylation in pneumonia mice in vivo. Conclusion: The results reveal that HHC attenuates pneumonia by targeted inhibition of JAK1/STAT3 signaling pathway. It indicates the novel role of HHC to treat pneumonia, and its potential applications for JAK inhibitortreated diseases.
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页数:13
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