Pharmacology and molecular docking study of cartilage protection of Chinese herbal medicine Fufang Shatai Heji (STHJ) by inhibiting the expression of MMPs in collagen-induced arthritis mice

被引:6
作者
Fan, Kai-Jian [1 ]
Li, Yun-Wu [1 ]
Wu, Jing [1 ]
Wang, Qi-Shan [1 ]
Xu, Bing-Xin [1 ]
Teng, Hui [1 ]
Chen, Si-Jia [1 ]
Wang, Ting-Yu [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Pharm, 639 Zhizaoju Rd, Shanghai 200011, Peoples R China
基金
中国国家自然科学基金;
关键词
Fufang Shatai Heji (STHJ); collagen-induced arthritis (CIA); cartilage; MMPs; ADAMTS; PRO-INFLAMMATORY CYTOKINES; RHEUMATOID-ARTHRITIS; MATRIX-METALLOPROTEINASE; DISEASE-ACTIVITY; ROSMARINIC ACID; PROTEOGLYCANS; DESTRUCTION; DEGRADATION; PATHWAY; ADAMTS5;
D O I
10.21037/apm-21-1765
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: This study aims to explore whether Fufang Shatai Heji (STHJ), as a mixture collected by a decoction of a variety of Chinese herbal medicines for immune system diseases, can improve the cartilage destruction of rheumatoid arthritis (RA). Methods: The therapeutic effects of STHJ were studied using collagen induced arthritis (CIA) mice. The improvement effect of STHJ on synovitis and cartilage damage caused by arthritis was studied by joint pathological analysis. The inhibitory effect of STHJ on related degradation enzymes in cartilage was studied by immunohistochemistry and real-time polymerase chain reaction (PCR). The specific targets of STHJ were predicted by molecular docking. Results: After successfully inducing CIA, the paws of the mice showed significant swelling, and athological analysis of the ankle and knee joints also showed significant cartilage destruction and synovial hyperplasia. However, synovial hyperplasia and cartilage destruction were markedly alleviated after administration of STHJ. And after SHTJ treatment, the expression of ADAMTS-4, ADAMTS-5, MMP-9 and MMP-13, in the cartilage layer of CIA mice was significantly inhibited. Through molecular docking assays, we proved that acteoside in STHJ could directly bind to the Glu111, Phe110 residues in MMP-9 and glycyrrhizic acid in STHJ bind to the Glu382, Asn433 residues in MMP-13. Conclusions: Our results suggested that STHJ may alleviate synovial hyperplasia and cartilage destruction in CIA mice and protect cartilage by inhibiting the expression of MMP-9 and other enzymes.
引用
收藏
页码:466 / 479
页数:14
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