非酒精性脂肪性肝炎
脂肪生成
炎症
乙二醇
活性氧
医学
化学
胆红素
内科学
非酒精性脂肪肝
药理学
生物化学
脂肪肝
新陈代谢
疾病
有机化学
作者
Jiahao Chen,Jinhang Zhang,Yan Xia,Jiahui Li,Qingyi Jia,Zijing Zhang,Xiandan Jing,Ying Xu,Ling Zou,Lingling Wang,Haiying Song,Jingwei Li,Qinhui Liu,Yimin Xiong,Qin Tang,Wenfei Chen,Na Yang,Haixia Xu,Yanping Li,Jinhan He
标识
DOI:10.1021/acs.molpharmaceut.4c00070
摘要
, and effectively scavenged intracellular ROS of hepatocytes. After systemic administration, DBZ Nps could accumulate in the liver of the NASH mice, extend persistence in circulation, and improve the bioavailability of DBZ. Furthermore, DBZ Nps significantly improved glucose intolerance, relieved hepatic lipid accumulation and inflammation, and ameliorated NASH-induced liver fibrosis. Additionally, DBZ Nps had no significant extrahepatic side effects. Taken together, our results highlight the potential of the ROS-sensitive DBZ nanoparticle as a promising therapeutic strategy for NASH.
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