Calycosin-7-O-β-D-glucoside attenuates palmitate-induced lipid accumulation in hepatocytes through AMPK activation

被引:7
|
作者
Xu, Wan [1 ]
Zhou, Feiye [2 ]
Zhu, Qin [3 ,4 ]
Bai, Mengyao [6 ]
Luo, Tiancheng [3 ,4 ]
Zhou, Libin [7 ]
Deng, Ruyuan [3 ,4 ,5 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Shanghai 200011, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Shanghai 200120, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Dept Gastroenterol & Hepatol, Shanghai 200032, Peoples R China
[4] Shanghai Inst Liver Dis, Shanghai 200032, Peoples R China
[5] Fudan Univ, Xiamen Branch, Dept Gastroenterol & Hepatol, Zhongshan Hosp, Xiamen 361006, Peoples R China
[6] Shanghai Jiao Tong Univ, Ruijin Hosp, Dept Endocrine & Metab Dis, Wuxi Branch,Sch Med, Wuxi 214145, Jiangsu, Peoples R China
[7] Shanghai Jiao Tong Univ, Shanghai Clin Ctr Endocrine & Metab Dis, Shanghai Inst Endocrine & Metab Dis, Dept Endocrine & Metab Dis,Ruijin Hosp,Sch Med, 197 Ruijin Rd 2, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
Calycosin-7-O-beta-D-glucoside; Hepatic steatosis; Hepatocyte; Lipogenesis; AMPK; FATTY LIVER-DISEASE; METABOLISM; PREVALENCE; MICROBIOTA; SREBP-1C; INSULIN; INJURY;
D O I
10.1016/j.ejphar.2022.174988
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Calycosin-7-O-beta-D-glucoside (CG) is the major component of Astragali Radix (AR), a traditional Chinese drug. As reported, CG could attenuate cerebral ischemia/reperfusion injury, protect blood-brain barrier integrity, and ameliorate myocardial infarction. To date, whether CG has a protective effect on metabolic diseases remains to be elucidated. In the present study, CG could attenuate palmitate-induced lipid accumulation in hepatocytes in a dose-dependent manner, with down-regulation of lipogenesis related genes expression and up-regulation of lipids beta-oxidation related genes expression. CG could decrease the triglyceride (TG) content from 0.30 mmol/g protein to 0.21 mmol/g protein and reduce the total cholesterol (TC) content from 0.39 mmol/g protein to 0.26 mmol/g protein. Moreover, CG stimulated the phosphorylation of AMP-activated protein kinase (AMPK), and the protective effect of CG on hepatocytes was partially reversed both by the inhibitor of AMPK signaling pathway and over-expression of AMPK-DN. Our findings revealed that CG could ameliorate palmitate-induced lipids accumulation in hepatocytes via AMPK activation and it may be a promising therapeutic medicine for hepatic steatosis.
引用
收藏
页数:8
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