Bifendate inhibits autophagy at multiple steps and attenuates oleic acid-induced lipid accumulation

被引:7
|
作者
Yuan, Weigang [1 ]
Jian, Fenglei [1 ]
Rong, Yueguang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Basic Med, Dept Pathogen Biol, Wuhan 430030, Peoples R China
关键词
Bifendate; Lysosome; Autophagy; Lipid droplet; ACUTE LIVER-INJURY; DERIVATIVES; CELLS; REFORMATION; P62/SQSTM1; EXPRESSION; LYSOSOMES; FUSION; MODEL; DRUG;
D O I
10.1016/j.bbrc.2022.09.067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Some traditional Chinese medicines exert roles in the therapy of liver diseases by modulating autophagy. Bifendate (DDB), a synthetic intermediate of Schisandrin C extracted from Schisandrae chinensis, is clin-ically used to treat hepatitis in China. While DDB is a positive control to research some potential hep-atoprotective agents, its related molecular mechanisms are unknown. In this study, we show that DDB inhibited autophagosome-lysosome fusion, lysosome acidification and autophagic lysosome reforma-tion. Moreover, DDB attenuated oleic acid-induced lipid droplet accumulation. These findings reveal the effects of DDB on the autophagy-related processes and lysosomal function, and also provide a possibility to understand the bioactivity mechanism of DDB in the future.(c) 2022 Published by Elsevier Inc.
引用
收藏
页码:115 / 123
页数:9
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