Liraglutide ameliorates non-alcoholic fatty liver disease by enhancing mitochondrial architecture and promoting autophagy through the SIRT1/SIRT3-FOXO3a pathway

被引:89
作者
Tong, Wenxin [1 ]
Ju, Liping [1 ]
Qiu, Miaoyan [1 ]
Xie, Qihai [2 ]
Chen, Ying [1 ]
Shen, Weili [2 ]
Sun, Weihong [3 ,4 ]
Wang, Weiqing [1 ]
Tian, Jingyan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Inst Endocrine & Metab Dis, Shanghai Clin Ctr Endocrine & Metab Dis, Dept Endocrinol & Metab,Sch Med,Ruijin Hosp, 197 Ruijin Er Rd, Shanghai 200033, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Inst Hypertens, Ruijin Hosp, Sch Med, Shanghai, Peoples R China
[3] Chinese Acad Sci, Inst Hlth Sci, Shanghai Inst Biol Sci, R107,Bldg 2,500 Caobao Rd, Shanghai 200033, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, R107,Bldg 2,500 Caobao Rd, Shanghai 200033, Peoples R China
基金
中国国家自然科学基金;
关键词
autophagy; liraglutide; mitochondrial architecture; oxidative stress; OXIDATIVE STRESS; ACCUMULATION; ROS; INDUCTION; DYNAMICS; MUSCLE; SIRT1;
D O I
10.1111/hepr.12634
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AimOverwhelming oxidative stress is implicated as crucial in the pathogenesis of non-alcoholic fatty liver disease (NAFLD). Liraglutide, a well-established antidiabetes drug, was recently reported to ameliorate NAFLD with an elusive mechanism. We used a mouse model to examine whether liraglutide could ameliorate NAFLD and explored the possible mechanisms. MethodsTwenty C57BL/6J mice were randomly treated with a normal-fat diet or high-fat diet for 16weeks, then further distributed into four groups and subjected to s.c. injection of liraglutide or saline for 4weeks. The growth/metabolism, oxidative stress, mitochondrial architecture and autophagy were assessed prospectively at the 20th week. ResultsHigh-fat diet inducement resulted in severe NAFLD while liraglutide treatment significantly reversed the trend, marked by reduced bodyweight, improved glucose tolerance and liver triglyceride composition. Reduced hepatic malondialdehyde level, increased mRNA and protein levels of CATALASE and MNSOD indicated liraglutide affected both the oxidative and antioxidative process to ameliorate oxidative stress. After liraglutide administration, the upregulated mRNA and protein levels of mitochondrial fission and fusion-related DRP1, OPA1 and respiratory chain-related COMPLEX1, UCP2 demonstrated the enhancement of mitochondrial architecture which may attenuate the generation of reactive oxygen species (ROS), while the diminished mRNA and protein level of P62 and increased levels of Beclin1 and LC3II/I ratio indicated the promoting autophagy, which probably contribute to the ROS elimination. Further, restored protein levels of Sirtuin1/Sirtuin3 and the downstream p-FOXO3a reveal the probable pathways of liraglutide acting on autophagy. ConclusionLiraglutide diminishes oxidative stress by enhancing mitochondrial architecture and promoting autophagy through the SIRT1/SIRT3-FOXO3a-LC3 pathway to ameliorate diet-induced NAFLD.
引用
收藏
页码:933 / 943
页数:11
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