药理学
炎症
类风湿性关节炎
医学
关节炎
免疫系统
佐剂
MMP3型
癌症研究
传统医学
免疫学
化学
生物化学
基因表达
基因
作者
Weiya Zeng,Caihong Shen,Suifen Mo,Ni Chen,Ying Lin,Yuan Fang,Huiling Yang,Guihua Luo,Luhua Xiao,Ruoting Zhan,Ping Yan
出处
期刊:Molecules
[MDPI AG]
日期:2023-01-02
卷期号:28 (1): 366-366
被引量:8
标识
DOI:10.3390/molecules28010366
摘要
Rubia cordifolia L. (Rubiaceae), one of the traditional anti-rheumatic herbal medicines in China, has been used to treat rheumatoid arthritis (RA) since ancient times. Purpurin, an active compound of Rubia cordifolia L., has been identified in previous studies and exerts antibacterial, antigenotoxic, anticancer, and antioxidant effects. However, the efficacy and the underlying mechanism of purpurin to alleviate RA are unclear. In this study, the effect of purpurin on inflammation was investigated using macrophage RAW264.7 inflammatory cells, induced by lipopolysaccharide (LPS), and adjuvant-induced arthritis (AIA) rat was established to explore the effect of purpurin on joint damage and immune disorders; the network pharmacology and molecular docking were integrated to dig out the prospective target. Purpurin showed significantly anti-inflammatory effect by reducing the content of IL-6, TNF-α, and IL-1β and increasing IL-10. Besides, purpurin obviously improved joint injury and hypotoxicity in the liver and spleen and regulated the level of FOXP3 and CD4+/CD8+. Furthermore, purpurin reduced the MMP3 content of AIA rats. Network pharmacology and molecular docking also suggested that MMP3 may be the key target of purpurin against RA. The results of this study strongly indicated that purpurin has a potential effect on anti-RA.
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