Exploring the pharmacological mechanism of Glycyrrhiza uralensis against KOA through integrating network pharmacology and experimental assessment

被引:0
作者
Xu, Jianbo [1 ,2 ,3 ]
Sun, Qi [4 ]
Qiu, Min [1 ,2 ]
Wu, Yungang [5 ]
Cheng, Liangyan [1 ,2 ]
Jiang, Nanwan [6 ]
Zhang, Ruogu [1 ,2 ,7 ]
Chen, Jiali [1 ,2 ,7 ]
Yuan, Wenhua [1 ,2 ,7 ]
Jin, Hongting [1 ,2 ,7 ]
Wang, Weidong [8 ]
Cai, Yunhuo [9 ]
Zhang, Chunchun [1 ,2 ]
Wang, Pinger [1 ,2 ,7 ]
机构
[1] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Zhejiang Prov Hosp Chinese Med, Inst Orthoped & Traumatol, Hangzhou, Peoples R China
[2] Zhejiang Chinese Med Univ, Coll Pharmaceut Sci, Hangzhou, Peoples R China
[3] Wenzhou Med Univ, Peoples Hosp Xiaoshan Dist 1, Xiaoshan Affiliated Hosp, Wenzhou, Peoples R China
[4] Hangzhou Fuyang Hosp TCM Orthopaed & Traumatol, Dept Orthoped Joint Surg, Hangzhou, Peoples R China
[5] Wenzhou Med Univ, Affiliated Hosp 1, Dept Orthoped TCM, Wenzhou, Peoples R China
[6] Hangzhou Yiyuan Pharmaceut Technol Co Ltd, Hangzhou, Peoples R China
[7] Zhejiang Chinese Med Univ, Coll Clin Med 1, Hangzhou, Peoples R China
[8] Zhejiang Chinese Med Univ, Affiliated Hosp 2, Dept Orthoped Surg, Hangzhou, Peoples R China
[9] Zhejiang Chinese Med Univ, Affiliated Hosp 3, Dept Orthoped Surg, Hangzhou, Peoples R China
关键词
Glycyrrhiza uralensis Fisch; inflammatory response; knee osteoarthritis; molecular docking; network pharmacology; OSTEOARTHRITIS;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Knee osteoarthritis (KOA), a major health and economic problem facing older adults worldwide, is a degenerative joint disease. Glycyrrhiza uralensis Fisch. (GC) plays an integral role in many classic Chinese medicine prescriptions for treating knee osteoarthritis. Still, the role of GC in treating KOA is unclear. To explore the pharmacological mechanism of GC against KOA, UPLC-Q-TOF/MS was conducted to detect the main compounds in GC. The therapeutic effect of GC on DMM-induced osteoarthritic mice was assessed by histomorphology, mu CT, behavioural tests, and immunohistochemical staining. Network pharmacology and molecular docking were used to predict the potential targets of GC against KOA. The predicted results were verified by immunohistochemical staining Animal experiments showed that GC had a protective effect on DMM-induced KOA, mainly in the improvement of movement disorders, subchondral bone sclerosis and cartilage damage. A variety of flavonoids and triterpenoids were detected in GC via UPLC-Q-TOF/MS, such as Naringenin. Seven core targets (JUN, MAPK3, MAPK1, AKT1, TP53, RELA and STAT3) and three main pathways (IL-17, NF-kappa B and TNF signalling pathways) were discovered through network pharmacology analysis that closely related to inflammatory response. Interestingly, molecular docking results showed that the active ingredient Naringenin had a good binding effect on anti-inflammatory-related proteins. In the verification experiment, after the intervention of GC, the expression levels of pp65 and F4/80 inflammatory indicators in the knee joint of KOA model mice were significantly downregulated. GC could improve the inflammatory environment in DMM-induced osteoarthritic mice thus alleviating the physiological structure and dysfunction of the knee joint. GC might play an important role in the treatment of knee osteoarthritis.
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页数:11
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