Pteryxin attenuates LPS-induced inflammatory responses and inhibits NLRP3 inflammasome activation in RAW264.7 cells

被引:29
作者
Zhen, Dong [1 ,2 ]
Xuan, Tian-qi [1 ,2 ]
Hu, Boqin [1 ,2 ]
Bai, Xue [1 ,2 ]
Fu, Dan-ni [1 ,2 ]
Wang, Yu [1 ,2 ]
Wu, Yun [3 ]
Yang, Jingfeng [4 ]
Ma, Qianqian [1 ,2 ]
机构
[1] Inner Mongolia Minzu Univ, Inst Pharmaceut Chem & Pharmacol, Tongliao 028000, Inner Mongolia, Peoples R China
[2] Inner Mongolia Key Lab Mongolian Med Pharmacol Ca, Tongliao 028000, Inner Mongolia, Peoples R China
[3] Inner Mongolia Minzu Univ, Affiliated Hosp, Tongliao 028000, Inner Mongolia, Peoples R China
[4] Inner Mongolia Minzu Univ, Coll Anim Sci & Technol, Tongliao 028000, Inner Mongolia, Peoples R China
基金
中国国家自然科学基金;
关键词
Pteryxin; Anti-inflammatory activity; NF-kappa B; MAPK; NLRP3; inflammasome; PEUCEDANUM-PRAERUPTORUM DUNN; NF-KAPPA-B; PYRANOCOUMARINS; COUMARINS; PURIFICATION; PATHWAYS; ROOT;
D O I
10.1016/j.jep.2021.114753
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Pteryxin is a natural coumarin compound that is found in "Qianhu", a traditional Chinese medicine, which possesses heat-clearing and detoxifying functions according to the theory of Traditional Chinese Medicine. Despite its medicinal effects, its anti-inflammatory and mechanisms of actions have not been established. Aim of this study: This study aims to evaluate the anti-inflammatory property and reveal the possible anti-inflammatory mechanisms of pteryxin. Material and methods: LPS-induced RAW 264.7 macrophages and LPS-induced zebrafish model were used for the anti-inflammatory activity determination of pteryxin. The level of NO, PEG(2), TNF-alpha and IL-6 were measured by ELISA. The accumulation of NO and ROS was stained and observed by a fluorescence microscopy. The nuclear translocation of NF-kappa B p65 and formation of NLRP3 inflammasome complex in LPS-induced RAW 264.7 macrophage cells were analyzed by immunofluorescence assay. The expression level of iNOS, IL-6, COX-2, TNF-alpha, p-p38, p38, ERK, JNK, p-ERK, p-JNK, IKK, I kappa B-alpha, p-IKK, p-p65, NLRP3, p-I kappa B-alpha, p65, Caspase 1 (p 20), ASC, and GAPDH were determined by Western blotting. Results: Lipopolysaccharide (LPS)-induced prostaglandin E2 (PGE2) and nitric oxide (NO) secretions were found to be downregulated by pteryxin. Moreover, pteryxin significantly suppressed inflammatory factor secretion in LPS-treated RAW 264.7 cells. Mechanistically, pteryxin significantly downregulated NF-kappa B/MAPK activation. Moreover, pteryxin inhibited caspase-1 and NLRP3 activation and formation of ASC specks in RAW 264.7 cells, implying that pteryxin inhibits inflammasome assembly, which is a signal for NLRP3 inflammasome activation. In conclusion, pteryxin blocks NF-kappa B/MAPK signaling, and suppresses the initiation and activation of NLRP3 thereby preventing inflammation. Conclusion: Pteryxin is a potential treatment option for inflammatory-related diseases.
引用
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页数:11
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