Evidence mapPaperPMID 41264140Full record

ArticleClinical rheumatology2026

Efficacy and potential toxicity of Duhuo Qinjiao Decoction in osteoarthritis via the NF-κB pathway.

Haiyang Kou, Rui Zhang, Jianbing Ma

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Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Haiyang KouDepartment of Joint Surgery, Honghui Hospital, Xi'an Jiaotong University, Xi'an 710000, Shaanxi, China.
Rui ZhangCollege of Medical Technology, Guiyang Healthcare Vocational University, Guiyang, Guizhou, 550081, China.
Jianbing MaDepartment of Joint Surgery, Honghui Hospital, Xi'an Jiaotong University, Xi'an 710000, Shaanxi, China. 13299028888@163.com.ORCID http://orcid.org/0000-0001-6321-3925

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the bioactivity, primary targets, and putative pharmacological processes of Duhuo Qinjiao Decoction (DHQJD) against osteoarthritis (OA), a network pharmacology and experimental validation strategy was employed.

methodsBiological activity, potential DHQJD targets, and OA-related targets were gathered from public databases. The key bioactive ingredients, potential targets, and signaling pathways were found using bioinformatics study, which included Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, Gene Ontology (GO), and protein-protein interaction (PPI). Molecular docking was then used to anticipate how active medications will attach to important targets.

resultsA total of 337 DHQJD active components and 94 DHQJD-related OA targets were assessed. Bioinformatics study indicated TNF, TP53, CASP3, and PTGS2 as potential therapeutic targets, while wogonin, myricanone, and beta-sitosterol were found as potential pharmacological possibilities. In mice with OA caused by destabilized medial meniscus (DMM), DHQJD was shown to be able to suppress the levels of inflammatory factors and the NF-kB signaling pathway. This further suggested that DHQJD's anti-OA actions could be mediated through the NF-kB signaling pathway.

conclusionThe findings provide a comprehensive understanding of the molecular processes, possible targets, and biological actions of DHQJD against OA. Additionally, it was demonstrated that DHQJD reduces inflammatory responses by inhibiting the activity of apoptotic effector caspase and the PI3K-Akt signaling pathway. There may be a need for novel herbs having anti-inflammatory and joint-protective qualities to help individuals with osteoarthritis. Key Points • DHQJD was widely prescribed in China during the Ming Dynasty for the treatment of osteoarthritic diseases. • With a history of nearly 1000 years, the formula has been centered on dispelling wind-dampness and clearing deficiency heat, and relieving paralyzing joint pain through the synergistic action of multiple herbs. • Recent studies in modern toxicology have found that there may be potential toxicity, but it may be minimal compared to the treatment of the disease, but the strength of the toxicity and the organs affected are still unknown.

Indexed as

Drugs, Chinese HerbalNF-kappa BOsteoarthritisAnimalsDisease Models, AnimalHumansMiceMolecular Docking SimulationNetwork PharmacologySignal TransductionDrugs, Chinese HerbalNF-kappa BDuhuo Qinjiao DecoctionExperimental validationNetwork pharmacologyOAOsteoarthritis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.