Evidence map›Paper›PMID 42535451›Full record

ArticleBiomedical chromatography : BMC2026

Zhuangdu Quhan Mixture Alleviates Ankylosing Spondylitis in Mice by Inhibiting the Interleukin-17 Signaling.

Dan Liu, Yanrong Wei, Zijing Ge, Qian Xu, Guoqian Deng, Peng Xiang, Lin Yang, Wen Zhang

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Dan LiuDepartment of Rheumatology, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.
Yanrong WeiOffice of Clinical Trial Institutions, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.ORCID https://orcid.org/0009-0008-4491-4361
Zijing GeDepartment of Rheumatology, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.
Qian XuDepartment of Rheumatology, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.
Guoqian DengGraduate School, Hunan University of Chinese Medicine, Changsha, China.
Peng XiangDepartment of Otolaryngology Head and Neck Surgery, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.
Lin YangDepartment of Rheumatology, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.ORCID https://orcid.org/0009-0005-6756-1683
Wen ZhangDepartment of General Medicine, The First Hospital of Hunan University of Chinese Medicine, Changsha, China.ORCID https://orcid.org/0009-0007-5497-9604

Funding

Excellent Youth Project of Hunan Provincial Department of Education 23B0386General Project of Hunan Provincial Administration of Traditional Chinese Medicine B2024060Key Project of Hunan Provincial Department of Education 23A0282Key Project of Hunan University of Chinese Medicine Joint Fund for 2024 2024XYLH339Open Fund for the 2024 Provincial and Ministerial Co-built National Key Laboratory Cultivation Base of Traditional Chinese Medicine Powder and Innovative Drugs 24PTKF1008Sub-project of the Key Research and Development Program of the Department of Science and Technology of Hunan Province 2024JK2130
6 · The paper itself

Abstract

This study aimed to elucidate the therapeutic effect and mechanism of Zhuangdu Quhan Mixture (ZDQHM) in ankylosing spondylitis (AS). An AS mouse model was established in mice using β-glucan. Therapeutic efficacy was assessed through arthritis scores, histopathology, serum cytokine measurement by ELISA, and bone metabolism-related protein analysis via Western blot. Active compounds were identified by UHPLC-MS, with targets predicted using network pharmacology and validated by molecular docking and molecular dynamics simulations. ZDQHM significantly ameliorated spinal inflammation and histopathological damage, reduced serum IL-6 and TNF-α levels, and modulated bone metabolism proteins. Network pharmacology identified 45 intersecting targets between ZDQHM compounds and AS, predominantly enriched in IL-17, Toll-like receptor, and NOD-like receptor pathways. Molecular docking and dynamics demonstrated binding of key compounds to IL-17A. In vivo validation revealed that ZDQHM suppressed IL-17A, Act1, and IL-17RA expression, and recombinant IL-17A partially reversed its therapeutic effects. ZDQHM alleviates inflammation and abnormal bone metabolism in AS mice, potentially through inhibition of the IL-17 signaling pathway. Beyond confirming the established role of IL-17 in AS, this study provides an integrated pharmacological framework explaining how ZDQHM exerts its effects via regulation of the IL-17A/IL-17RA/Act1 axis, offering mechanistic insights and experimental support for TCM in AS therapy.

Indexed as

Drugs, Chinese HerbalInterleukin-17Signal TransductionSpondylitis, AnkylosingAnimalsChromatography, High Pressure LiquidDisease Models, AnimalMaleMiceMolecular Docking SimulationMolecular Dynamics SimulationDrugs, Chinese HerbalInterleukin-17ankylosing spondylitisbone metabolisminterleukin‐17 signaling pathwaymolecular dockingmolecular dynamics simulationnetwork pharmacologytraditional Chinese medicineultra‐high‐performance liquid chromatography‐mass spectrometryZhuangdu Quhan Mixture

Identifiers

PMID42535451
PMCPMC13425452

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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 OpenQuestion graph.