The Anti-Osteoporosis Effects of Panax japonicus via Downregulation of Inflammatory Factors: A Network Pharmacology and Ovariectomized Rat Model Study.

IF 2
Yumiao Zhang, Yang Liu, Yuchen Zhang, Xinbo Shi, Yingang Li, Yalei Pan
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Abstract

Objective: Osteoporosis is a major and growing public health problem characterized by decreased bone mineral density and destroyed bone microarchitecture. Panax japonicus has been clinically used in the treatment of bone diseases, especially osteoporosis. However, there is a lack of study on the mechanism of osteoporosis treatment with Panax japonicus.

Materials and methods: A network pharmacology approach was employed to identify the targets of osteoporosis and Panax japonicus. Cytoscape 3.7.2 and DAVID were used to visualize the pharmacological mechanism of Panax japonicus in treating osteoporosis by building up compound-target and protein-protein interaction (PPI) networks and conducting Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses. An ovariectomized SD rat osteoporosis model was used to assess the potential therapeutic effect of Panax japonicus in vivo. The biomechanical properties, pathological changes, inflammatory cytokines, bone density, and bone microstructural parameters in rat bone tissue were carefully measured. The biochemical markers of bone metabolism in serum were detected by Enzyme-Linked Immunosorbent Assay (ELISA).

Results: Fifty-two active components and sixty-five target genes of Panax japonicus involved in the treatment of osteoporosis were identified. The PPI network revealed IL-6, TNF, NR3C1, IL-1β, CASP3, ESR1, PGR, and AR to be involved in the treatment of osteoporosis with Panax japonicus. Chikusetsusaponin IVa and Radix ginsenoside-Ro were the main saponins found in Panax japonicus. Panax japonicus was found to exert potent preventive effects on osteoporosis by maintaining biomechanical properties, increasing bone mineral density, and protecting the trabecular microstructure in an ovariectomized rat osteoporosis model. Panax japonicus hindered the initiation of osteoporosis induced by ovariectomy by regulating bone metabolism and downregulating the expression of IL-6 and TNF-α.

Conclusion: Panax japonicus was found to contain 52 compounds and 65 targets in the treatment of osteoporosis. The administration of Panax japonicus could mitigate osteoporosis in rats induced by ovariectomy, and one of the mechanisms was associated with downregulating the expression of inflammatory factors.

参芪通过下调炎性因子的抗骨质疏松作用:网络药理学及去卵巢大鼠模型研究。
目的:骨质疏松症是一个日益严重的重大公共卫生问题,其特征是骨密度降低和骨微结构破坏。参已被临床用于治疗骨病,尤其是骨质疏松症。然而,对参芪治疗骨质疏松的作用机制尚缺乏研究。材料与方法:采用网络药理学方法对参芪和骨质疏松症靶点进行鉴定。利用Cytoscape 3.7.2和DAVID构建化合物靶点和蛋白-蛋白相互作用(PPI)网络,并进行基因本体(GO)和京都基因与基因组百科全书(KEGG)途径富集分析,可视化日本参治疗骨质疏松的药理机制。采用去卵巢SD大鼠骨质疏松模型,在体内评价刺参对骨质疏松的潜在治疗作用。仔细测量大鼠骨组织的生物力学特性、病理变化、炎症因子、骨密度和骨微结构参数。采用酶联免疫吸附试验(ELISA)检测血清骨代谢生化指标。结果:鉴定出参芪治疗骨质疏松的52种有效成分和65个靶基因。PPI网络显示IL-6、TNF、NR3C1、IL-1β、CASP3、ESR1、PGR和AR参与参芪治疗骨质疏松症。七苦参皂苷IVa和人参皂苷ro是七苦参中主要的皂苷类化合物。在去卵巢大鼠骨质疏松模型中,我们发现日本参通过维持生物力学性能、增加骨矿物质密度和保护骨小梁结构,对骨质疏松症有明显的预防作用。参通过调节骨代谢,下调IL-6、TNF-α的表达,抑制卵巢切除所致骨质疏松的发生。结论:参芪中含有52种化合物,65个靶点,具有治疗骨质疏松的作用。参对卵巢切除大鼠骨质疏松有一定的缓解作用,其机制之一可能与下调炎性因子的表达有关。
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