Ramulus Mori (Sangzhi) Alkaloids Alleviate High-Fat Diet-Induced Obesity and Nonalcoholic Fatty Liver Disease in Mice

被引:35
|
作者
Chen, Yan-Min [1 ,2 ,3 ]
Lian, Chun-Fang [1 ,2 ,3 ]
Sun, Qian-Wen [1 ,2 ,3 ]
Wang, Ting-Ting [4 ]
Liu, Yuan-Yuan [4 ]
Ye, Jun [1 ,2 ,3 ]
Gao, Li-Li [1 ,2 ,3 ]
Yang, Yan-Fang [1 ,2 ,3 ]
Liu, Shuai-Nan [1 ,2 ]
Shen, Zhu-Fang [1 ,2 ]
Liu, Yu-Ling [1 ,2 ,3 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing 100050, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100050, Peoples R China
[3] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing Key Lab Drug Delivery Technol & Novel For, Beijing 100050, Peoples R China
[4] Tsinghua Univ, Sch Pharmaceut Sci, Beijing 100084, Peoples R China
关键词
NAFLD; obesity; Ramulus Mori (Sangzhi) alkaloids; steatosis; oxidative stress; adiponectin; OXIDATIVE STRESS; PATHOGENESIS; MITOCHONDRIA; ADIPONECTIN; STEATOHEPATITIS; METABOLISM; ADIPOR1;
D O I
10.3390/antiox11050905
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
Nonalcoholic fatty liver disease (NAFLD), obesity, and type 2 diabetes mellitus (T2DM) have highly related mechanisms. Ramulus Mori (Sangzhi) alkaloids (SZ-A) from Morus alba L. were approved in 2020 for the treatment of T2DM. In this study, we examined the therapeutic effects and mechanism of SZ-A on obesity and NAFLD in mice. Mice (C57BL/6J) fed a high-fat diet (HFD) for 14 weeks were treated with SZ-A for another 6 weeks. HFD-induced weight gain was reduced by SZ-A in a dose-dependent manner. SZ-A treatment significantly stimulated adiponectin expression and secretion in adipose tissue and 3T3-L1 adipocytes. Additionally, SZ-A markedly reduced hepatic steatosis (triglyceride, total cholesterol) and expression of pro-inflammatory and pro-fibrotic genes. SZ-A regulated lipid metabolism and oxidative stress (malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx), and glutathione (GSH)) in the liver. Palmitic acid-induced insulin resistance and lipid accumulation in HepG2 cells were also repressed by SZ-A. Collectively, SZ-A protected mice from HFD-induced NAFLD through an indirect effect of improved systemic metabolism reducing bodyweight, and a direct effect by enhancing the lipid metabolism of HepG2 cells. The weight-loss effect of SZ-A in mice was partly due to improved fatty oxidation instead of influencing food consumption.
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页数:19
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