肥胖
脂肪变性
脂肪组织
白藜芦醇
疾病
自噬
医学
脂肪肝
非酒精性脂肪肝
代谢综合征
肝细胞
代谢性疾病
肝病
下调和上调
胰岛素
胰岛素抵抗
生物信息学
内科学
内分泌学
白色脂肪组织
药理学
糖尿病
罗格列酮
代谢紊乱
合成代谢
作者
Qiaqia Xiao,Chuying Wang,H. J. Yang,Xueyu Gao,Zhaoan Chen,Zheming Niu,Yi Hou,Cong Fu,Ziwei Yan,Guangda Zhu,Hening Liu,Yue Yin,Jing Shang,Wei Wang,Lu Tang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-10-08
卷期号:25 (42): 15416-15427
被引量:4
标识
DOI:10.1021/acs.nanolett.5c04561
摘要
Obesity manifests as excessive fat storage within adipose tissue (AT) and is often accompanied by insulin resistance, which can initiate the development of obesity-related metabolic dysfunction-associated steatotic liver disease (MASLD). Herein, a dual-targeting drug delivery system is designed to regulate these metabolic disorders by alleviating aberrant fat accumulation and anti-inflammation. Specifically, polymetformin (P) and resveratrol (R), two therapeutic agents that show preferable antiadiposity effect, are co-loaded in macrophage-disguised and apolipoprotein A-I (apoA-I)-decorated liposome (aML/R&P). Mechanistically, P and R can upregulate uncoupling protein 1 (UCP1) expression to promote AT browning and enhance hepatocyte autophagy to ameliorate hepatic steatosis and inflammation. Meanwhile, the dual modification of macrophage membrane and apoA-I largely improves its targeting efficiency toward liver and AT. In mouse models of obesity and MASLD, aML/R&P effectively reduces body weight, restores metabolic homeostasis, enhances liver parameters, and improves insulin sensitivity, demonstrating great promise in treating obesity and obesity-associated metabolic disorders.
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