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Research Article | Open Access

Honeysuckle-derived exosome-like nanovesicles ameliorate metabolic-associated fatty liver disease by modulating gut microbiota and its metabolites

Ping Li1,2,3,§Qingyuan Wu5,§Yuanhao Zhou3,4Xiaojuan Hu3,4Yan Tang3,4Yuanyuan Wang3,4Weijiao Fan3,4Yiyi Shan1,3,4Kexin Yu1,3,4Jie Wang6Shibing Wang7Xiao Ye8 ( )Huiyu Liu5 ( )Xiaozhou Mou1,3,4 ( )
Center for Rehabilitation Medicine, Rehabilitation and Sports Medicine Research Institute of Zhejiang Province, Department of Rehabilitation Medicine, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou 310014, China
College of Pharmacy, Zhejiang University of Technology, Hangzhou 310014, China
General Surgery, Cancer Center, Department of Hepatobiliary & Pancreatic Surgery and Minimally Invasive Surgery, Zhejiang Provincial People’s Hospital, Affiliated People’s Hospital, Hangzhou Medical College, Hangzhou 310014, China
Key Laboratory of Tumor Molecular Diagnosis and Individualized Medicine of Zhejiang Province, Clinical Research Institute, Zhejiang Provincial People’s Hospital, Affiliated People’s Hospital, Hangzhou Medical College, Hangzhou 310014, China
Beijing Advanced Innovation Center for Soft Matter Science and Engineering, State Key Laboratory of Organic-Inorganic Composites, Bionanomaterials and Translational Engineering Laboratory, Beijing Key Laboratory of Bioprocess, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing 100029, China
EVital Bio (Hangzhou) Co., Ltd, Hangzhou 310056, China
Department of Clinical Laboratory, Affiliated Hangzhou First People’s Hospital, School of Medicine, Westlake University, Hangzhou 310006, China
Center for General Practice Medicine, Department of Endocrinology, Zhejiang Provincial People’s Hospital, Affiliated People's Hospital, Hangzhou Medical College, Hangzhou 310014, China

§ Ping Li and Qingyuan Wu contributed equally to this work.

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Abstract

Metabolic-associated fatty liver disease (MAFLD), a global health burden with limited therapeutic options beyond lifestyle changes, urgently needs novel strategies. We engineered exosome-like nanovesicles (HNVs) from dried honeysuckle (Lonicera japonica), exhibiting significantly more uniform size distribution than conventional herbal extracts and characteristic nanovesicle morphology. Orally delivered HNVs, enriched with bioactive metabolites, dramatically inhibited increased fat vacuoles, lipid droplet deposition, and collagen fibrosis in the livers of mice with MAFLD induced by high-fat diet (HFD). Mechanistically, HNVs orchestrate a dual gut-liver intervention: (1) restoring gut barrier integrity, slashing serum LPS by 1.58-fold and quelling hepatic inflammation; (2) remodeling gut microbiota to suppress bile salt hydrolase (BSH), elevating taurochenodeoxycholic acid (TCDCA) 2.07-fold. This microbial shift reprograms enterohepatic signaling by inhibiting the FXR-FGF15-FGFR4 axis, thereby boosting hepatic cholesterol catabolism via bile acid synthases. Critically, efficacy is strictly microbiota-dependent: abolished by antibiotics and fully transferable via fecal microbiota transplantation (FMT) from HNV-treated donors. Presenting the first natural nanovesicle platform that concurrently targets gut barrier repair and metabolic reprogramming, HNVs establish a pioneering, multi-targeted therapeutic paradigm for MAFLD, directly linking gut microbial ecology to hepatic pathophysiology with high translational potential.

Graphical Abstract

In this study, we developed exosome-like nanovesicles derived from dried honeysuckle (HNVs), which significantly ameliorated the pathological condition of metabolism-associated fatty liver disease (MAFLD) through a dual modulation of the gut-liver axis—on one hand suppressing hepatic immune-inflammatory responses and on the other promoting the decomposition of cholesterol (TC) and triglycerides (TG).

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Cite this article:
Li P, Wu Q, Zhou Y, et al. Honeysuckle-derived exosome-like nanovesicles ameliorate metabolic-associated fatty liver disease by modulating gut microbiota and its metabolites. Nano Research, 2025, 18(12): 94907986. https://doi.org/10.26599/NR.2025.94907986
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Received: 03 July 2025
Revised: 21 August 2025
Accepted: 23 August 2025
Published: 07 November 2025
© The Author(s) 2025. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).