Network Pharmacology Unveils Multi-Systemic Intervention of Panax notoginseng in Osteoporosis via Key Genes and Signaling Pathways.

Qiyue Wang, Xiaoping Wang, Kezhou Wu, Weiwei Wu, Zhantu Wei, Weili Feng
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Abstract

Background: Panax notoginseng (Burk.) F. H. Chen (PN) is a traditional Chinese medicine that has been applied to prevent and treat osteoporosis. The mechanism of PN for osteoporosis remained a mystery.

Objective: The objective was to reveal the therapeutic effect and illuminate the possible mechanism of PN for osteoporosis.

Methods: The Traditional Chinese Medicine Database and Analysis Platform was searched to screen the potent ingredients of the PN and to analyze the potential therapeutic targets for osteoporosis. We excavated four disease databases to collect osteoporosis-related genes. After integrating the gene expression profile of osteoporosis and the chemical-protein data of PN, a protein-protein interaction network was constructed to demonstrate the interactions among the gene products. GO function, KEGG pathway, and docking analyses were executed.

Results: Network pharmacology obtained 31 active ingredients and 134 targets for the treatment of osteoporosis. The key components were beta-elemene, quercetin, methyl palmitate, oleic acid, and hexanal. The results of GO and KEGG analyses showed that Panax notoginseng was beneficial for osteoporosis by influencing the main pathways including AGE-RAGE signaling pathway in diabetic complications, TNF signaling pathway, IL-17 signaling pathway, p53 signaling pathway, NF-kappa B signaling pathway, PI3K-Akt signaling pathway, MAPK signaling pathway, FoxO signaling pathway, and Wnt signaling pathway, modulating inflammation, metabolism, cell proliferation, cell survival, growth and angiogenesis. Panax notoginseng intervened in osteoporosis through multi-components, multi-targets, and multi-pathways.

Conclusion: This study illustrates the mechanism of Panax notoginseng for osteoporosis, providing broader insights for novel research and developments of the Panax species for osteoporosis.

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网络药理学揭示三七通过关键基因和信号通路对骨质疏松的多系统干预。
背景:三七(Burk.)陈霞芬(PN)是一种用于预防和治疗骨质疏松症的中药。PN治疗骨质疏松的机制仍是一个谜。目的:揭示PN治疗骨质疏松症的疗效及可能的机制。方法:检索中药数据库和分析平台,筛选PN有效成分,分析其治疗骨质疏松的潜在靶点。我们挖掘了四个疾病数据库来收集骨质疏松相关基因。结合骨质疏松基因表达谱和PN化学蛋白数据,构建蛋白-蛋白相互作用网络,展示基因产物之间的相互作用。执行GO函数、KEGG通路和对接分析。结果:网络药理学获得治疗骨质疏松症的有效成分31种,靶点134个。主要成分为-榄香烯、槲皮素、棕榈酸甲酯、油酸和己醛。GO和KEGG分析结果显示,三七通过影响糖尿病并发症中AGE-RAGE信号通路、TNF信号通路、IL-17信号通路、p53信号通路、NF-kappa B信号通路、PI3K-Akt信号通路、MAPK信号通路、FoxO信号通路和Wnt信号通路等主要通路,调节炎症、代谢、细胞增殖、细胞存活、生长和血管生成,对骨质疏松症有一定的治疗作用。三七通过多组分、多靶点、多途径干预骨质疏松症。结论:本研究阐明了三七治疗骨质疏松的作用机制,为三七治疗骨质疏松的新研究和开发提供了更广阔的思路。
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