# Combined treatment with naringin and osthole ameliorates colitis through microbiota–amino acid metabolism and the JNK pathway

**Authors:** Mengqin Chen, Zihao Lu, Tong Zhang, Guoping Li, Qingyu Zheng, Tao Zhang

PMC · DOI: 10.1007/s13659-025-00582-z · Natural Products and Bioprospecting · 2026-02-04

## TL;DR

Combining naringin and osthole helps treat colitis by improving gut health and reducing inflammation.

## Contribution

This study reveals the combined effects of naringin and osthole on colitis via microbiota, amino acid metabolism, and the JNK pathway.

## Key findings

- Naringin and osthole together reduce colitis symptoms more effectively than individual treatments.
- The combination downregulates the JNK/NF-κB pathway and repairs the intestinal barrier.
- Metabolomic analysis shows amino acid metabolism, especially tryptophan, is a key pathway affected.

## Abstract

Inflammatory bowel disease (IBD), particularly ulcerative colitis, involves disruption of the intestinal mucosal barrier due to ecological and metabolic imbalances in the gut as its underlying pathology. Current therapies for Ulcerative colitis (UC) exhibit limited efficacy and adverse effects, necessitating the development of novel treatment strategies. Naringin and osthole are natural herbal compounds that show therapeutic potential in various inflammatory models due to their excellent anti-inflammatory activity. However, their combined therapeutic effects and precise mechanisms in UC remain unreported. This study aimed to explore the therapeutic effectiveness and mechanism of naringin combined with osthole in addressing dextran sodium sulfate (DSS)-induced colitis. The investigation centered on their impact on the disruption of the intestinal epithelial cell barrier, modulation of intestinal flora composition, alteration of metabolites, and inflammation model in vitro. Modal assessment encompassed body weight, disease activity index (DAI) score, colon length, and histopathological examination. Intestinal barrier integrity was evaluated through Quantitative Real-Time PCR, western blotting, and immunofluorescence staining. Microbiota abundance and metabolic levels were assessed using 16S ribosomal RNA gene sequencing and metabolomics analysis. Protein expression levels of pertinent pathways and associated receptors were tested through network pharmacology prediction and western blot analysis. Naringin and osthole synergistically relieved colitis symptoms in mice compared with either drug alone or 5-aminosalicylic acid, as evidenced by weight loss recovery, DAI scores, and colon length preservation. Mechanistically, naringin combined with osthole down-regulated the expression level of JNK/NF-κB signaling pathway related proteins and repaired intestinal barrier. Furthermore, the combination regulates the composition of the microflora and promotes the restoration of a steady state of the microflora. Metabolomic revealed amino acid-tryptophan metabolism as a key metabolic pathway. It also reveals the microbiota-tryptophan pathway as a potential therapeutic strategy. Naringin combined with osthole can alleviate DSS-induced colitis more effectively by JNK/NF-κB signaling pathway, repairing barrier function and regulating intestinal microbiota and metabolites. These findings provide a theoretical basis for the combination therapy strategy to enhance the efficacy of potential functional food in treating ulcerative colitis.

## Linked entities

- **Proteins:** MAPK8 (mitogen-activated protein kinase 8), NFKB1 (nuclear factor kappa B subunit 1)
- **Chemicals:** naringin (PubChem CID 442428), osthole (PubChem CID 10228), 5-aminosalicylic acid (PubChem CID 4075)
- **Diseases:** inflammatory bowel disease (MONDO:0005265), ulcerative colitis (MONDO:0005101)

## Full-text entities

- **Genes:** Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, Birc5 (baculoviral IAP repeat-containing 5) [NCBI Gene 11799] {aka AAC-11, Api4, TIAP, survivin40}, Mapk8 (mitogen-activated protein kinase 8) [NCBI Gene 26419] {aka JNK, JNK1, Prkm8, SAPK1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}, Jun (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 16476] {aka AP-1, Junc, c-jun}, MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599] {aka JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, 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}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Mapk14 (mitogen-activated protein kinase 14) [NCBI Gene 26416] {aka CSBP2, Crk1, Csbp1, Mxi2, PRKM14, PRKM15}, Mpo (myeloperoxidase) [NCBI Gene 17523] {aka mKIAA4033}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}
- **Diseases:** metabolic disorder (MESH:D008659), weight gain (MESH:D015430), Inflammatory (MESH:D007249), diarrhea (MESH:D003967), arthritis (MESH:D001168), endometritis (MESH:D004716), colon cancer (MESH:D015179), immune dysfunction (MESH:D007154), cervical dislocation (MESH:D002575), weight loss (MESH:D015431), pancreatitis (MESH:D010195), intestinal diseases (MESH:D007410), IBD (MESH:D015212), inflammatory damage (MESH:D018746), hemorrhagic (MESH:D006470), Cytotoxicity (MESH:D064420), neuropathic pain (MESH:D009437), UC (MESH:D003093), chronic pain (MESH:D059350), splenomegaly (MESH:D013163), Colitis (MESH:D003092), infection (MESH:D007239)
- **Chemicals:** SP600125 (MESH:C432165), CCK-8 (MESH:D012844), H (MESH:D006859), LPS (MESH:D008070), Osthole (MESH:C046627), corn oil (MESH:D003314), CO2 (MESH:D002245), paraffin (MESH:D010232), NAD+ (MESH:D009243), Hematoxylin (MESH:D006416), urea (MESH:D014508), eosin (MESH:D004801), carbohydrates (MESH:D002241), O (MESH:D010100), H&amp;E (MESH:D006371), PVDF (MESH:C024865), paraformaldehyde (MESH:C003043), penicillin (MESH:D010406), streptomycin (MESH:D013307), ethanol (MESH:D000431), DMSO (MESH:D004121), Quinolinate (MESH:D017378), SCFA (MESH:D005232), xylene (MESH:D014992), oligosaccharides (MESH:D009844), 5-ASA (MESH:D019804), 7-methoxy-8-(3-methylbut-2-enyl) chromen-2-one (-), indole (MESH:C030374), Naringin (MESH:C005274), polyphenols (MESH:D059808), DAPI (MESH:C007293), Tryptophan (MESH:D014364), Dextran sulfate sodium (MESH:D016264), olive oil (MESH:D000069463), coumarin (MESH:C030123), kynurenine (MESH:D007737), agarose (MESH:D012685), amino acid (MESH:D000596), TRIzol (MESH:C411644), aminosalicylates (MESH:D010131), Formalin (MESH:D005557), N (MESH:D009584), SDS (MESH:D012967)
- **Species:** Lactobacillus (genus) [taxon 1578], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Bacteroidia (class) [taxon 200643], Homo sapiens (human, species) [taxon 9606], Bacteroides (genus) [taxon 816], Mus musculus (house mouse, species) [taxon 10090], Pseudomonadota (proteobacteria, phylum) [taxon 1224], Escherichia coli (E. coli, species) [taxon 562], Bos taurus (bovine, species) [taxon 9913], Angelica pubescens (du huo, species) [taxon 312530], Cnidium monnieri (species) [taxon 94007], Akkermansia (genus) [taxon 239934], Canis lupus familiaris (dog, subspecies) [taxon 9615], Curcuma longa (turmeric, species) [taxon 136217], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12868363/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868363/full.md

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Source: https://tomesphere.com/paper/PMC12868363