肠道菌群
金银花
外体
脂肪肝
化学
微生物学
生物
疾病
细胞生物学
生物化学
医学
微泡
内科学
基因
病理
小RNA
中医药
替代医学
作者
Ping Li,Qingyuan Wu,Yuanhao Zhou,Xiaojuan Hu,Yan Tang,Yuan-yuan Wang,Weijiao Fan,Yiyi Shan,Kexin Yu,Jie Wang,Shibing Wang,Ye Xiao,Huiyu Liu,Xiaozhou Mou
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2025-08-26
卷期号:18 (12): 94907986-94907986
被引量:1
标识
DOI:10.26599/nr.2025.94907986
摘要
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.
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