Two Birds with One Stone: Guanidyl Carbon Dots with Enhanced Antioxidative and Lipolytic Functions in Metabolic Associated Fatty Liver

被引:37
作者
Cai, Hao [1 ]
Li, Yan [1 ]
Wu, Xiaoyan [1 ]
Yang, Yuxiang [2 ]
Tedesco, Antonio Claudio [3 ]
Li, Zijian [1 ]
Bi, Hong [1 ]
机构
[1] Anhui Univ, Sch Mat Sci & Engn, Hefei 230601, Peoples R China
[2] Anhui Univ, Sch Chem & Chem Engn, Hefei 230601, Peoples R China
[3] Univ Sao Paulo, Fac Philosophy Sci & Letters Ribeirao Preto, Ctr Nanotechnol & Tissue Engn, Dept Chem,Photobiol & Photomed Res Grp, BR-14040901 Ribeirao Preto, SP, Brazil
基金
国家重点研发计划;
关键词
antioxidation; carbon dot; guanidine group; lipid metabolism; metabolic associated fatty liver disease; HEPATIC STEATOSIS; DISEASE; AMPK; ZEBRAFISH; AUTOPHAGY; PATHWAY; GROWTH; AGENTS;
D O I
10.1002/adfm.202406096
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metabolic-associated fatty liver disease (MAFLD) has become one of the most widespread metabolic diseases nowadays, while no definitive agent is approved for practical treatment. Given excessive lipid deposition and cellular oxidative stress are two main inducers of MAFLD, developing synergistic therapeutic agents that enhance lipid metabolism and antioxidative ability are effective routes for MAFLD therapy. Herein, a novel kind of bio-functional carbon dots (MTCDs) derived from metformin and tea polyphenols based on a fused pharmacophore strategy is developed. The surface of MTCDs retains abundant phenolic hydroxyl and guanidine groups, which are designed to reduce both lipid deposition and oxidative stress in the liver. Moreover, by finely controlling the surface charge, MTCDs exhibit excellent lysosome targeting functionality with favorable biocompatibility and low biotoxicity. Mechanistical studies further reveal that MTCDs treatment protects lysosomes from oxidative stress damage and activates hepatocyte AMP-activated protein kinase signaling, which initiates lipophagy progress to accelerate lipolysis and lipid consumption. Collectively, these studies propose an effective "two birds with one stone" tool for MAFLD synergistic therapy and suggest a viable strategy for multi-pharmacophore agent development.
引用
收藏
页数:10
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