Evidence map›Paper›PMID 41853904›Full record

ArticleJournal of cellular and molecular medicine2026

Honokiol and Magnolol Exert an Anti-Inflammatory Effect by Inhibiting JAK2/STAT3/IL17 Signalling in a Rat Model of Ulcerative Colitis: A Combination of Bioinformatics and Experimental Study.

Zhaoxu Cai, Shaojun Lu, Jingan Chen, Xiaoshan Yang, Junlin Lu, Changwen Feng

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

6 authors.

Zhaoxu CaiDepartment of Pharmacy, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Shaojun LuLaboratory Animal Center, Guangdong Pharmaceutical University, Guangzhou, China.
Jingan ChenDepartment of Pharmacy, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Xiaoshan YangDepartment of Pharmacy, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Junlin LuDepartment of Pharmacy, The First People's Hospital of Zhaoqing, Zhaoqing, China.
Changwen FengDepartment of Pharmacy, The First People's Hospital of Zhaoqing, Zhaoqing, China.ORCID 0009-0007-8694-350X

Funding

Guangdong Provincial Bureau of Traditional Chinese Medicine, Chinese Medicine Research Project 20221216Guangdong Provincial Bureau of Traditional Chinese Medicine, Chinese Medicine Research Project 20221457Wu Jieping Medical Research Grant 320.6750.2024-6-108Zhaoqing First Hospital Research Grant YJJ-2023-02-02Zhaoqing First Hospital Research Grant YJJ-2025-01-016
6 · The paper itself

Abstract

Ulcerative colitis (UC) is a chronic, inflammatory bowel disease with limited clinical treatment. Traditional Chinese medicinal ingredients honokiol and magnolol have potential anti-inflammatory and gastrointestinal protective effects. However, their anti-inflammatory potential has not been investigated in UC. This study hypothesized that honokiol and magnolol alleviate UC by targeting key inflammatory signalling pathways. To verify this, we established a 2,4-dinitrobenzenesulfonic acid-induced UC rat model and administered honokiol and magnolol orally. The results showed that the two ingredients significantly reduced the disease activity index and colonic mucosal damage index and downregulated serum levels of pro-inflammatory factors TNF-α, IL-17, and CRP. Histopathological examination showed marked alleviation of colonic mucosal hyperemia, inflammatory infiltration, and ulcerative damage following honokiol and magnolol treatment. Bioinformatics analysis identified 74 UC-related targets for honokiol and 62 for magnolol, which were enriched in inflammatory response and JAK-STAT/IL-17 signalling pathways. A gradient boosting machine model was established to screen 16 shared hub targets, among which IL17A, JAK2, and STAT3 were highly correlated with immune cell infiltration. Molecular docking confirmed that honokiol and magnolol could stably bind to key proteins of the JAK-STAT pathway via noncovalent interactions with low binding energy. Immunohistochemistry and Western blot further verified that both ingredients significantly inhibited the activation of IL17A, JAK2, and STAT3 in the colonic tissues of UC rats. This study demonstrates that honokiol and magnolol exert anti-inflammatory effects in UC rats by inhibiting the JAK2/STAT3/IL17 pathway, providing a mechanistic basis and potential targets for the application of traditional Chinese medicinal ingredients in UC treatment.

Indexed as

Anti-Inflammatory AgentsBiphenyl CompoundsColitis, UlcerativeInterleukin-17Janus Kinase 2LignansSignal TransductionSTAT3 Transcription FactorAllyl CompoundsAnimalsComputational BiologyDisease Models, AnimalMaleMolecular Docking SimulationPhenolsRatsAllyl CompoundsAnti-Inflammatory AgentsBiphenyl CompoundshonokiolInterleukin-17Jak2 protein, ratJanus Kinase 2LignansmagnololPhenolsStat3 protein, ratSTAT3 Transcription Factoranti‐inflammationhonokiol and magnololIL17JAK2/STAT3ulcerative colitis

Identifiers

PMID41853904
PMCPMC13097488

What Socratic holds

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LicenceCC BY
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Registered trials

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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.