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Published in: Journal of Orthopaedic Surgery and Research 1/2024

Open Access 01-12-2024 | Lumbar Disc Herniation | Research article

Mechanism exploration of Osteoking in the treatment of lumbar disc herniation based on network pharmacology and molecular docking

Authors: Xinlei Luo, Jingjing Liu, Xiaoxi Wang, Qiaojun Chen, Yanfa Lei, Zewei He, Xiaowei Wang, Yan Ye, Qiang Na, Changtao Lao, Zhengchang Yang, Jun Jiang

Published in: Journal of Orthopaedic Surgery and Research | Issue 1/2024

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Abstract

Objective

Lumbar disc herniation (LDH) is a common spinal surgical disease. Low back and leg pain caused by LDH is the main factor leading to functional disability, which has caused a serious burden to patients and society. Osteoking can delay the progression of osteoporosis and osteoarthritis, and even has a significant effect on the prevention of deep vein thrombosis after fracture surgery. In recent years, it has been gradually used in the treatment of LDH and has received significant results. However, the underlying mechanism remains unclear. The aim of this study was to predict the mechanism of Osteoking in the treatment of LDH through network pharmacology and verify it by molecular docking method.

Methods

The TCMSP database was used to collect the relevant active components and targets of Osteoking, while the GeneCards, OMIM and DisGeNET databases were utilized to collect the relevant disease targets of LDH. The Venny 2.1.0 software was employed to obtain the intersecting gene targets of Osteoking and LDH. PPI network construction and core target selection were performed using Cytoscape 3.9.0 software. The Metascape database was used for GO and KEGG enrichment analysis of the relevant targets. Finally, molecular docking was conducted using AutoDock software.

Results

The study identified 116 potential targets and 26 core targets for the treatment of LDH with Osteoking. Pathways in cancer, Alzheimer's disease, microRNAs in cancer and the IL-17 signalling pathway were among the main involved signalling pathways. Molecular docking results demonstrated that the key targets AKT1, IL-6, ALB, TNF and IL-1β exhibited relatively stable binding activities with the main active components of Osteoking.

Conclusions

Osteoking can alleviate the symptoms of lumbar disc herniation through the modulation of multiple targets and signalling pathways.
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Metadata
Title
Mechanism exploration of Osteoking in the treatment of lumbar disc herniation based on network pharmacology and molecular docking
Authors
Xinlei Luo
Jingjing Liu
Xiaoxi Wang
Qiaojun Chen
Yanfa Lei
Zewei He
Xiaowei Wang
Yan Ye
Qiang Na
Changtao Lao
Zhengchang Yang
Jun Jiang
Publication date
01-12-2024
Publisher
BioMed Central
Published in
Journal of Orthopaedic Surgery and Research / Issue 1/2024
Electronic ISSN: 1749-799X
DOI
https://doi.org/10.1186/s13018-024-04570-w

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