First College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China (mainland).
Department of Orthopedics, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China (mainland).
Med Sci Monit. 2019 Aug 1;25:5700-5716. doi: 10.12659/MSM.915170.
d_abstr_R Rhizoma drynariae is the main traditional Chinese medicine used for the treatment of osteoporosis, but its anti-osteoporotic targeting mechanism has not been fully elucidated due to the complexity of its active ingredients. In this study, the pharmacological mechanism of action of Rhizoma drynariae against osteoporosis was studied by integrating pharmacological concepts. The pharmacokinetic characteristics of selected major active constituents of Rhizoma drynariae and the SMILES structural similarity were used to predict related targets. A literature search was conducted to identify known osteoporosis treatment targets, which were then combined with the predicted targets to construct the direct or indirect target interaction network map of Rhizoma drynariae against osteoporosis. Finally, data on the key targets of the interactions, ranked according to relevant node parameters obtained through pathway enrichment analysis and screening of key targets and active ingredients of Rhizoma drynariae, were used to perform molecular docking simulation. We screened 16 active ingredients of Rhizoma drynariae, and 7 key targets with direct or indirect effects with a high frequency were obtained. These main pathways were found to play important roles in the PI3k-akt signaling pathway, osteoclast differentiation, Wnt signaling pathway, and estrogen signaling pathway. Molecular docking showed that most active ingredients of Rhizoma drynariae had strong binding efficiency with key targets. Based on network pharmacology, we conclude that Rhizoma drynariae plays an anti-osteoporotic role by directly or indirectly targeting multiple major signaling pathways and influencing the proliferation and differentiation of multiple types of cells.
骨碎补是治疗骨质疏松症的主要中药,但由于其活性成分复杂,其抗骨质疏松作用机制尚未完全阐明。本研究通过整合药理学概念,研究了骨碎补治疗骨质疏松症的药理作用机制。利用所选骨碎补主要活性成分的药代动力学特征和 SMILES 结构相似性,预测相关靶点。通过文献检索,确定了已知的骨质疏松症治疗靶点,然后将这些靶点与预测的靶点相结合,构建了骨碎补治疗骨质疏松症的直接或间接靶点相互作用网络图谱。最后,根据通路富集分析和骨碎补关键靶点及活性成分筛选得到的相关节点参数,对相互作用的关键靶点进行数据排名,用于进行分子对接模拟。筛选出骨碎补 16 种活性成分,得到具有直接或间接高频率作用的 7 个关键靶点。这些主要通路在 PI3k-akt 信号通路、破骨细胞分化、Wnt 信号通路和雌激素信号通路中发挥重要作用。分子对接表明,骨碎补的大多数活性成分与关键靶点具有很强的结合效率。基于网络药理学,我们得出结论,骨碎补通过直接或间接靶向多个主要信号通路,影响多种类型细胞的增殖和分化,发挥抗骨质疏松作用。