Using network pharmacology and molecular docking technology, proteomics and experiments were used to verify the effect of Yigu decoction (YGD) on the expression of key genes in osteoporotic mice.

Annals of medicine Pub Date : 2025-12-01 Epub Date: 2025-01-03 DOI:10.1080/07853890.2024.2449225
Kun Yan, Rui-Kun Zhang, Jia-Xin Wang, Hai-Feng Chen, Yang Zhang, Feng Cheng, Yi Jiang, Min Wang, Ziqi Wu, Xiao-Gang Chen, Zhi-Neng Chen, Gui-Jin Li, Xin-Miao Yao
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Abstract

Background: Yigu decoction (YGD) is a traditional Chinese medicine prescription for the treatment of osteoporosis, although many clinical studies have confirmed its anti-OP effect, but the specific mechanism is still not completely clear.

Methods: In this study, through the methods of network pharmacology and molecular docking, the material basis and action target of YGD in preventing and treating OP were analyzed, and the potential target and mechanism of YGD in preventing and treating OP were clarified by TMT quantitative protein and experiment.

Results: Network pharmacology and molecular docking revealed that the active components of YGD were mainly stigmasterol and flavonoids. Molecular docking mainly studied the strong binding ability of stigmasterol to the target. Animal proteomics verified the related mechanism of YGD in preventing and treating OP. Based on the KEGG enrichment of network pharmacology and histology, our animal experiments in vivo verified that YGD may play a role in the treatment of OP by mediating hif1- α/vegf/glut1 signal pathway.

Conclusions: YGD prevention and treatment of OP may be achieved by interfering with multiple targets. This study confirmed that it may promote osteoblast proliferation and protect osteoblast function by up-regulating the expression of proteins related to HIF signal pathway.

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采用网络药理学和分子对接技术,结合蛋白质组学和实验验证益骨汤对骨质疏松小鼠关键基因表达的影响。
背景:益骨汤(YGD)是治疗骨质疏松症的中药方剂,虽然许多临床研究证实其抗op作用,但具体机制尚不完全清楚。方法:本研究通过网络药理学和分子对接的方法,分析YGD预防和治疗OP的物质基础和作用靶点,并通过TMT定量蛋白和实验阐明YGD预防和治疗OP的潜在靶点和机制。结果:网络药理学和分子对接发现,黄酮类化合物主要为豆甾醇和黄酮类化合物。分子对接主要研究了豆甾醇对靶标的强结合能力。动物蛋白质组学验证了YGD预防和治疗OP的相关机制。基于网络药理学和组织学的KEGG富集,我们的动物体内实验验证了YGD可能通过介导hif1- α/vegf/glut1信号通路,在OP的治疗中发挥作用。结论:通过多靶点干扰,可实现对OP的YGD防治。本研究证实其可能通过上调HIF信号通路相关蛋白的表达,促进成骨细胞增殖,保护成骨细胞功能。
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