The therapeutic effect of Fufang Zhenshu Tiaozhi (FTZ) on osteoclastogenesis and ovariectomized-induced bone loss: evidence from network pharmacology, molecular docking and experimental validation

• Published in: Aging (Albany, NY.) Vol. 14; no. 14; pp. 5727 - 5748
• Main Authors: Chen, Xiaojun, Wang, Jiangyan, Tang, Lin, Ye, Qiuying, Dong, Qunwei, Li, Zhangwei, Hu, Li, Ma, Chenghong, Xu, Jiake, Sun, Ping
• Format: Journal Article
• Language: English
• Published: United States Impact Journals 12.07.2022
• Subjects: Animals; Bone Resorption - drug therapy; Cell Differentiation; Female; Mice; Molecular Docking Simulation; Network Pharmacology; Osteogenesis; Ovariectomy; Research Paper; Tumor Necrosis Factor-alpha - pharmacology; Fufang Zhenshu Tiaozhi; molecular docking; osteoclast; osteoporosis; network pharmacology
• ISSN: 1945-4589; 1945-4589
• DOI: 10.18632/aging.204172

Fufang Zhenshu Tiaozhi (FTZ) has been widely used in clinical practice and proven to be effective against aging-induced osteoporosis in mice. This study aimed to explore the mechanism of FTZ against osteoclastogenesis and ovariectomized-induced (OVX) bone loss through the network pharmacology approach. The ingredients of FTZ were collected from the previous UPLC results, and their putative targets were obtained through multiple databases. Differentially expressed genes (DEGs) during osteoclastogenesis were identified through multi-microarrays analysis. The common genes between FTZ targets and DEGs were used to perform enrichment analyses through the clusterProfier package. The affinity between all FTZ compounds and enriched genes was validated by molecular docking. The effects of FTZ on osteoclastogenesis and bone resorption were evaluated by TRAP staining, bone resorption assay and RT-qPCR , while its effects on bone loss by ELISA and Micro-CT . Enrichment analyses indicated that the inhibitory effects of FTZ may primarily involve the regulation of inflammation, osteoclastogenesis, as well as TNF-α signaling pathway. 130 pairs docking results confirmed FTZ ingredients have good binding activities with TNF-α pathway enriched genes. FTZ treatment significantly reduced TRAP, TNF-α, IL-6 serum levels and increased bone volume in OVX mice. Consistently, experiments revealed that FTZ-containing serum significantly inhibited osteoclast differentiation, bone resorption, and osteoclast related mRNA expression. This study revealed the candidate targets of FTZ and its potential mechanism in inhibiting osteoclastogenesis and bone loss induced by OVX, which will pave the way for the application of FTZ in the postmenopausal osteoporosis treatment.