College of Traditional Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.
Key Laboratory of Chinese Medicinal Resources from Lingnan (Guangzhou University of Chinese Medicine), Ministry of Education, Guangzhou, People's Republic of China.
Drug Des Devel Ther. 2023 Feb 11;17:439-457. doi: 10.2147/DDDT.S388932. eCollection 2023.
L. (RC) is a classic herbal medicine for the treatment of rheumatoid arthritis (RA) and has been used since ancient times. The ethanol extract of L. (RCE) showed obvious anti-RA effects in our previous study. However, further potential mechanisms require more exploration. We aimed to investigate the mechanism of RCE for the treatment of RA by integrating metabolomics and network pharmacology in this study.
An adjuvant-induced arthritis (AIA) rat model was established, and we evaluated the therapeutic effects of RCE. Metabolomics of serum and urine was used to identify the differential metabolites. Network pharmacology was applied to determine the key metabolites and potential targets. Finally, the potential targets and compounds of RCE were verified by molecular docking.
The results indicated that RCE suppressed foot swelling and alleviated joint damage and also had anti-inflammatory properties by inhibiting the expressions of tumor necrosis factor (TNF)-α, Interleukin (IL)-1β, prostaglandin E2 (PGE2), and P65. Ten and seven differential metabolites were found in the serum and urine, respectively, of rats. Six key targets, ie, phospholipase A2 group IIA (PLA2G2A), phospholipase A2 group X (PLA2G10), cytidine deaminase (CDA), uridine-cytidine kinase 2 (UCK2), charcot-leyden crystal galectin (CLC), and 5',3'-nucleotidase, mitochondrial (NT5M), were discovered by network pharmacology and metabolite analysis and were found to be related to glycerophospholipid metabolism and pyrimidine metabolism. Molecular docking confirmed that the favorable compounds showed affinities with the key targets, including alizarin, 6-hydroxyrubiadin, ruberythric acid, and munjistin.
This study revealed the underlying mechanisms of RCE and provided evidence that will allow researchers to further investigate the functions and components of RCE against RA.
山豆根是一种治疗类风湿关节炎(RA)的经典草药,自古以来就被使用。我们之前的研究表明,山豆根的乙醇提取物(RCE)对 RA 具有明显的抗 RA 作用。然而,进一步的潜在机制需要更多的探索。本研究旨在通过整合代谢组学和网络药理学来研究 RCE 治疗 RA 的机制。
建立佐剂诱导关节炎(AIA)大鼠模型,评价 RCE 的治疗效果。采用血清和尿液代谢组学方法鉴定差异代谢物。应用网络药理学确定关键代谢物和潜在靶点。最后,通过分子对接验证 RCE 的潜在靶点和化合物。
结果表明,RCE 通过抑制肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β、前列腺素 E2(PGE2)和 P65 的表达,抑制足肿胀,缓解关节损伤,具有抗炎作用。大鼠血清和尿液中分别发现 10 种和 7 种差异代谢物。网络药理学和代谢物分析发现 6 个关键靶点,即磷脂酶 A2 组 IIA(PLA2G2A)、磷脂酶 A2 组 X(PLA2G10)、胞苷脱氨酶(CDA)、尿苷-胞苷激酶 2(UCK2)、胆堿酯酶-莱登晶体半乳糖凝集素(CLC)和 5',3'-核苷酸酶,线粒体(NT5M)。分子对接证实,有利的化合物与关键靶点具有亲和力,包括茜素、6-羟基蒽醌、ruberythric 酸和 munjistin。
本研究揭示了 RCE 的潜在机制,并为进一步研究 RCE 对 RA 的功能和成分提供了证据。