Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritis

Abstract Background Osteoarthritis (OA), a leading cause of disability worldwide, is characterized by complex interactions between cartilage degradation and synovial inflammation. While NSAIDs are the primary treatment, their prolonged use exacerbates gastrointestinal risks and does not alter diseas...

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Main Authors: Jingyi Hou, Yubo Li, Yu Zhang, Ning Yang, Bin Chen, Guiyun Ma, Naiqiang Zhu
Format: Article
Language:English
Published: BMC 2025-05-01
Series:BMC Complementary Medicine and Therapies
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Online Access:https://doi.org/10.1186/s12906-025-04928-5
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author Jingyi Hou
Yubo Li
Yu Zhang
Ning Yang
Bin Chen
Guiyun Ma
Naiqiang Zhu
author_facet Jingyi Hou
Yubo Li
Yu Zhang
Ning Yang
Bin Chen
Guiyun Ma
Naiqiang Zhu
author_sort Jingyi Hou
collection DOAJ
description Abstract Background Osteoarthritis (OA), a leading cause of disability worldwide, is characterized by complex interactions between cartilage degradation and synovial inflammation. While NSAIDs are the primary treatment, their prolonged use exacerbates gastrointestinal risks and does not alter disease progression. Xianlinggubao (XLGB), an approved Chinese herbal remedy for osteoporosis, has demonstrated promising anti-osteoarthritic effects in preliminary studies. However, its multi-component mechanisms targeting OA-related inflammation require further clarification. This study integrates network pharmacology with experimental validation to investigate XLGB's anti-inflammatory mechanisms in OA. Methods Bioactive compounds of XLGB and their respective targets were sourced from the TCMSP, ETCM, SymMap, and ChEMBL databases. Targets linked to OA-related inflammation were identified through differential expression analysis and by querying OMIM, GeneCards, and PubMed Gene databases. Network pharmacology and bioinformatics approaches were employed to construct compound-target and protein–protein interaction (PPI) networks, enabling the identification of pivotal therapeutic targets. Functional enrichment of these targets was performed using the ClusterProfiler package in R. The binding affinity of compounds to anti-inflammatory OA targets was assessed through molecular docking, dynamics simulations, RT-PCR, and immunofluorescence assays. Results Fifty-five bioactive compounds corresponding to 475 XLGB targets and 125 genes involved in OA-related inflammation were identified. PPI network analysis revealed that XLGB may alleviate OA inflammation by modulating key genes, including COX-2, IL-1β, TNF, IL-6, and MMP-9. Molecular simulations indicated strong binding affinities between bioactive compounds in XLGB and these critical targets. Functional enrichment analysis suggested that XLGB's anti-inflammatory action in OA may involve regulation of pathways such as IL-17, TNF, and NF-κB. In vitro experiments further confirmed that XLGB mitigates OA inflammation by modulating these genes, proteins, and signaling pathways. Conclusions Through network pharmacology, this study elucidated the mechanisms of XLGB in OA inflammation, highlighting its modulation of IL-6, IL-1β, TNF-α, PTGS2, MMP-9, and the NF-κB pathway. These findings provide strong support for the clinical application of XLGB in managing OA-related inflammation.
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spelling doaj-art-0efc7a1db9604d508b07d63f35d039f92025-08-20T03:16:33ZengBMCBMC Complementary Medicine and Therapies2662-76712025-05-0125112210.1186/s12906-025-04928-5Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritisJingyi Hou0Yubo Li1Yu Zhang2Ning Yang3Bin Chen4Guiyun Ma5Naiqiang Zhu6Hebei Province Key Laboratory of Study and Exploitation of Chinese Medicine, Institute of Traditional Chinese Medicine, Chengde Medical UniversityDepartment of Minimally Invasive Spinal Surgery, The Affiliated Hospital of Chengde Medical UniversityDepartment of Minimally Invasive Spinal Surgery, The Affiliated Hospital of Chengde Medical UniversityDepartment of Minimally Invasive Spinal Surgery, The Affiliated Hospital of Chengde Medical UniversityDepartment of Minimally Invasive Spinal Surgery, The Affiliated Hospital of Chengde Medical UniversityDepartment of Minimally Invasive Spinal Surgery, The Affiliated Hospital of Chengde Medical UniversityDepartment of Minimally Invasive Spinal Surgery, The Affiliated Hospital of Chengde Medical UniversityAbstract Background Osteoarthritis (OA), a leading cause of disability worldwide, is characterized by complex interactions between cartilage degradation and synovial inflammation. While NSAIDs are the primary treatment, their prolonged use exacerbates gastrointestinal risks and does not alter disease progression. Xianlinggubao (XLGB), an approved Chinese herbal remedy for osteoporosis, has demonstrated promising anti-osteoarthritic effects in preliminary studies. However, its multi-component mechanisms targeting OA-related inflammation require further clarification. This study integrates network pharmacology with experimental validation to investigate XLGB's anti-inflammatory mechanisms in OA. Methods Bioactive compounds of XLGB and their respective targets were sourced from the TCMSP, ETCM, SymMap, and ChEMBL databases. Targets linked to OA-related inflammation were identified through differential expression analysis and by querying OMIM, GeneCards, and PubMed Gene databases. Network pharmacology and bioinformatics approaches were employed to construct compound-target and protein–protein interaction (PPI) networks, enabling the identification of pivotal therapeutic targets. Functional enrichment of these targets was performed using the ClusterProfiler package in R. The binding affinity of compounds to anti-inflammatory OA targets was assessed through molecular docking, dynamics simulations, RT-PCR, and immunofluorescence assays. Results Fifty-five bioactive compounds corresponding to 475 XLGB targets and 125 genes involved in OA-related inflammation were identified. PPI network analysis revealed that XLGB may alleviate OA inflammation by modulating key genes, including COX-2, IL-1β, TNF, IL-6, and MMP-9. Molecular simulations indicated strong binding affinities between bioactive compounds in XLGB and these critical targets. Functional enrichment analysis suggested that XLGB's anti-inflammatory action in OA may involve regulation of pathways such as IL-17, TNF, and NF-κB. In vitro experiments further confirmed that XLGB mitigates OA inflammation by modulating these genes, proteins, and signaling pathways. Conclusions Through network pharmacology, this study elucidated the mechanisms of XLGB in OA inflammation, highlighting its modulation of IL-6, IL-1β, TNF-α, PTGS2, MMP-9, and the NF-κB pathway. These findings provide strong support for the clinical application of XLGB in managing OA-related inflammation.https://doi.org/10.1186/s12906-025-04928-5Bioinformatics analysisHub geneNetwork pharmacologyNF-κBOsteoarthritisXianlinggubao prescription
spellingShingle Jingyi Hou
Yubo Li
Yu Zhang
Ning Yang
Bin Chen
Guiyun Ma
Naiqiang Zhu
Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritis
BMC Complementary Medicine and Therapies
Bioinformatics analysis
Hub gene
Network pharmacology
NF-κB
Osteoarthritis
Xianlinggubao prescription
title Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritis
title_full Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritis
title_fullStr Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritis
title_full_unstemmed Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritis
title_short Integrated network pharmacology reveals the mechanism of action of Xianlinggubao prescription for inflammation in osteoarthritis
title_sort integrated network pharmacology reveals the mechanism of action of xianlinggubao prescription for inflammation in osteoarthritis
topic Bioinformatics analysis
Hub gene
Network pharmacology
NF-κB
Osteoarthritis
Xianlinggubao prescription
url https://doi.org/10.1186/s12906-025-04928-5
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