# Oxymatrine for inflammatory bowel disease in preclinical studies: a systematic review and meta-analysis

**Authors:** Xuan Zhao, Xiaolu Ye, Yuting Gu, Yijie Lou, Zhanyi Zhou, Yunxi Ji, Daogun Xu

PMC · DOI: 10.3389/fmed.2025.1542953 · Frontiers in Medicine · 2025-04-30

## TL;DR

This study reviews preclinical evidence showing that oxymatrine may help treat inflammatory bowel disease by reducing inflammation and improving intestinal health in animal models.

## Contribution

A systematic review and meta-analysis of oxymatrine's effects on IBD in preclinical studies, revealing its potential therapeutic mechanisms.

## Key findings

- Oxymatrine reduced inflammation markers like IL-6, IL-1β, and TNF-α in IBD animal models.
- Oxymatrine improved intestinal barrier function by increasing ZO-1 and occludin expression.
- Oxymatrine extended colon length and lowered disease activity in IBD models.

## Abstract

Inflammatory Bowel Disease (IBD) is a chronic, idiopathic inflammatory disorder of the intestines. Oxymatrine (OMT) is a naturally active substance found in the desiccated roots of Sophora flavescens. It possesses anti-tumor, antiviral, and anti-inflammatory properties. In recent years, its therapeutic role in IBD has gradually been discovered. This review aims to explore the impact of OMT on inflammatory bowel disease by animal models.

Conduct a systematic search in the PubMed, Embase, Web of Science, Cochrane, and Medline databases. Using SYRCLE’s risk of bias tool to assess the bias risk and quality of the included studies. For some data presented as figures, Web Plot Digitizer 4.2 software was used to extract it. STATA 16.0 was selected for the final meta-analysis.

After rigorous literature screening, 12 studies were included. The data analysis results indicated that the disease activity index (DAI), histopathological score (HS), interleukin-6 (IL-6), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), nuclear factor-κB (NF-κB), and myeloperoxidase (MPO) activity in the IBD animal models significantly decreased following intervention with oxymatrine. Furthermore, OMT also extended the colon length in the animal models and improved the expression level of zonula occludens-1(ZO-1) and occludin. These results suggested that OMT may improve the condition of IBD through anti-inflammatory, antioxidative stress and protecting the intestinal barrier.

Meta-analysis suggests oxymatrine positively affects IBD animal models. This provides new insights for the clinical treatment of inflammatory bowel disease.

https://www.crd.york.ac.uk/PROSPERO/view/CRD42024570580, identifier [CRD42024570580].

## Linked entities

- **Proteins:** IL6 (interleukin 6), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3)
- **Chemicals:** Oxymatrine (PubChem CID 114850)
- **Diseases:** Inflammatory Bowel Disease (MONDO:0005265)

## Full-text entities

- **Genes:** SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, Mpo (myeloperoxidase) [NCBI Gene 17523] {aka mKIAA4033}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Rhoa (ras homolog family member A) [NCBI Gene 11848] {aka Arha, Arha1, Arha2}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Nfkbia (nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha) [NCBI Gene 18035] {aka Nfkbi}, IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620] {aka IDO, IDO-1, INDO}, TIMP1 (TIMP metallopeptidase inhibitor 1) [NCBI Gene 7076] {aka CLGI, EPA, EPO, HCI, TIMP, TIMP-1}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, PIK3CG (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma) [NCBI Gene 5294] {aka IMD97, PI3CG, PI3K, PI3Kgamma, PIK3, p110gamma}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, MPO (myeloperoxidase) [NCBI Gene 4353], PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, DUOX2 (dual oxidase 2) [NCBI Gene 50506] {aka LNOX2, NOXEF2, P138-TOX, TDH6, THOX2}
- **Diseases:** CD (MESH:D003424), DAI (MESH:C566784), Ulcerative (MESH:D014456), liver and kidney damage (MESH:D056486), cardiovascular diseases (MESH:D002318), toxicity (MESH:D064420), hepatitis B (MESH:D006509), IBD (MESH:D015212), UC (MESH:D003093), diabetes (MESH:D003920), skin diseases (MESH:D012871), tissue damage (MESH:D017695), Colitis (MESH:D003092), liver fibrosis (MESH:D008103), Inflammation (MESH:D007249), weight loss (MESH:D015431), cancers (MESH:D009369)
- **Chemicals:** GSH (MESH:D005978), lipid (MESH:D008055), 2,4,6-trinitrobenzene sulfonic acid (-), oxaliplatin (MESH:D000077150), MDA (MESH:D008315), mesalazine (MESH:D019804), OMT (MESH:C037573), hydroperoxides (MESH:D006861), aminosalicylic acid (MESH:D010131), NO (MESH:D009614), PBS (MESH:D007854), DSS (MESH:D016264), free radicals (MESH:D005609), ROS (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Sophora flavescens (species) [taxon 49840]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12075229/full.md

## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC12075229/full.md

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Source: https://tomesphere.com/paper/PMC12075229