# Broccoli-Derived Exosome-like Nanoparticles Alleviates Metabolic Dysfunction-Associated Steatotic Liver Disease Through Modulating the Gut–Liver Axis

**Authors:** Feng Zhang, Ruolan Liu, Tongxiao Xu, Wentao Xu, Kunlun Huang, Xiaoyun He

PMC · DOI: 10.3390/nu18060953 · Nutrients · 2026-03-18

## TL;DR

Broccoli-derived nanoparticles may help treat a common liver disease by improving gut and liver health.

## Contribution

Shows broccoli-derived nanoparticles can reduce liver disease by modulating the gut-liver axis.

## Key findings

- BDENs reduced liver weight and ALT/AST ratio in mice with MASLD.
- BDENs improved gut barrier function and bile acid metabolism.
- BDENs suppressed liver inflammation markers like IL-6 and IL-1β.

## Abstract

Background/Objectives: Metabolic dysfunction-associated steatohepatitis (MASLD) represents a prevalent liver disease worldwide. It is crucial to maintain the stability of the gut–liver axis in order to inhibit the advancement of MASLD. Broccoli-derived exosome-like nanoparticles (BDENs) can alleviate constipation and improve colitis. This study investigated whether BDENs possess therapeutic potential for improving induced MASLD by the gut–liver axis. Methods: BDENs were fractionated from fresh broccoli using differential centrifugation, and the microRNAs were identified and analyzed. 24 male C57BL/6J mice (6 weeks old) were randomized into the control group, HFD group, and BDENs group, with 8 mice per group. After 8 weeks of high-fat diet modeling, the BDENs group accepted BDENs daily oral gavage of 100 mg/kg (B.W.), while the control and HFD groups accepted 1 × PBS. Four weeks after BDENs intervention, analysis was conducted on liver injury markers, liver tissue pathology, intestinal barrier, cecal content metabolomics and fecal 16S rRNA, serum inflammatory factors, and hepatic inflammation. Results: BDENs identified 1659 miRNAs associated with physiological processes such as immunity, antioxidant defense, and fatty acid biosynthesis. BDENs significantly reduced weight and ALT/AST ratio (p < 0.05). Furthermore, BDENs attenuated hepatic histopathological damage and lipid accumulation. For the gut–liver axis, BDENs maintained intestinal barrier, regulated intestinal bile acid metabolism and restored the gut microbiota. Additionally, BDENs reduced serum LPS level (p < 0.01) and suppressed hepatic inflammation, including F4/80 and IL-6, IL-1β (p < 0.0001). Conclusions: Oral BDENs therapy demonstrates potential for ameliorating MASLD.

## Linked entities

- **Diseases:** Metabolic dysfunction-associated steatohepatitis (MONDO:0007027), MASLD (MONDO:0013209)

## Full-text entities

- **Genes:** Tmprss11d (transmembrane protease, serine 11d) [NCBI Gene 231382] {aka AST, AsP}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Gpt (glutamic pyruvic transaminase, soluble) [NCBI Gene 76282] {aka 1300007J06Rik, 2310022B03Rik, ALT, ALT1, Gpt-1, Gpt1}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Adgre1 (adhesion G protein-coupled receptor E1) [NCBI Gene 13733] {aka DD7A5-7, EGF-TM7, Emr1, F4/80, Gpf480, Ly71}
- **Diseases:** Metabolic dysfunction-associated steatohepatitis (MESH:D005234), hepatic inflammation (MESH:D007249), liver injury (MESH:D017093), colitis (MESH:D003092), Steatotic Liver Disease (MESH:D008107), constipation (MESH:D003248), Metabolic Dysfunction (MESH:D008659), hepatic histopathological damage (MESH:D056486)
- **Chemicals:** lipid (MESH:D008055), fat (MESH:D005223), LPS (MESH:D008070), bile acid (MESH:D001647), PBS (MESH:D007854), fatty acid (MESH:D005227)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13029203/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029203/full.md

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Source: https://tomesphere.com/paper/PMC13029203