Shaanxi University of Chinese Medicine, Shaanxi Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, State Key Laboratory of Research & Development of Characteristic Qin Medicine Resources (Cultivation), Shaanxi Province Key Laboratory of New Drugs and Chinese Medicine Foundation Research, 712083, Xianyang, PR China.
Shaanxi University of Chinese Medicine, Shaanxi Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, State Key Laboratory of Research & Development of Characteristic Qin Medicine Resources (Cultivation), Shaanxi Province Key Laboratory of New Drugs and Chinese Medicine Foundation Research, 712083, Xianyang, PR China.
Biomed Pharmacother. 2020 Sep;129:110052. doi: 10.1016/j.biopha.2020.110052. Epub 2020 Jun 16.
Radix Paeoniae Rubra (RPR) is a traditional Chinese medicine with anti-inflammatory effects that has been used in chronic pelvic inflammation disease (CPID) therapy. However, research on the mechanism of RPR in CPID therapy is lacking. Here, we used a network pharmacology method to screen targets and found that the PTGS2 target in the arachidonic acid (AA) pathway was significantly related to CPID. Then, regarding the molecular mechanism, it was further confirmed that RPR may reduce the development of CPID by regulating the PTGS2 target. The CPID rat model was established by mixed bacterial infection. We verified the expression of PTGS2 by immunohistochemical analysis, western blotting assays to detect the expression of PTGS2 protein, and polymerase chain reaction detection of PTGS2 mRNA expression. It was observed that the PTGS2 target decreased significantly after RPR administration at different doses. It is suggested that RPR can reverse the abnormal expression of PTGS2 in CPID rats. We believe that RPR is effective in the treatment of CPID, and RPR can reduce the inflammatory symptoms of CPID by regulating the level of PTGS2 in the AA pathway.
赤芍是一种具有抗炎作用的中药,用于治疗慢性盆腔炎。然而,赤芍治疗 CPID 的作用机制研究尚缺乏。在这里,我们采用网络药理学方法筛选靶点,发现 AA 通路中的 PTGS2 靶点与 CPID 显著相关。然后,关于分子机制,进一步证实赤芍可能通过调节 PTGS2 靶点来减轻 CPID 的发展。通过混合细菌感染建立 CPID 大鼠模型。通过免疫组织化学分析验证 PTGS2 的表达,Western blot 检测 PTGS2 蛋白的表达,聚合酶链反应检测 PTGS2 mRNA 表达。观察到赤芍在不同剂量给药后 PTGS2 靶点明显减少。这表明赤芍可以逆转 CPID 大鼠中 PTGS2 的异常表达。我们认为赤芍对 CPID 有效,赤芍可以通过调节 AA 通路中 PTGS2 的水平来减轻 CPID 的炎症症状。