Penthorum chinense Pursh extract ameliorates alcohol-related fatty liver disease in mice via the SIRT1/AMPK signaling axis

被引:0
|
作者
Hui, Zhuge [1 ,4 ]
Pan, Yan [1 ,4 ]
Lai, Shanglei [1 ,4 ]
Chang, Kaixin [1 ,4 ]
Ding, Qinchao [2 ,3 ,4 ]
Cao, Wenjing [2 ]
Song, Qing [2 ]
Li, Songtao [2 ]
Dou, Xiaobing [1 ,4 ]
Ding, Bin [1 ,4 ]
机构
[1] Zhejiang Chinese Med Univ, Coll Life Sci, Hangzhou 310053, Peoples R China
[2] Zhejiang Chinese Med Univ, Coll Publ Hlth, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Coll Anim Sci, Hangzhou 310058, Peoples R China
[4] Zhejiang Chinese Med Univ, Mol Med Inst, Hangzhou 310053, Peoples R China
基金
浙江省自然科学基金;
关键词
Penthorum chinense Pursh; Alcohol-related fatty liver disease; SIRT1; AMPK; Lipid metabolism; Graphical abstract; HEPATIC STEATOSIS; OXIDATIVE STRESS; CHRONIC ETHANOL; EMERGING ROLES; CONTRIBUTES; INSULIN; PATHOGENESIS; INHIBITION; RESISTANT; TARGETS;
D O I
10.1016/j.heliyon.2024.e31195
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Penthorum chinense Pursh (P. chinense), a functional food, has been applied to protect the liver against alcohol-related fatty liver disease (ALD) for a long history in China. This study was designed to evaluate the ameliorative activity of the polyphenolic fraction in P. chinense (PGF) depending on the relief of ALD. The ALD mouse model was established by exposing the mice to a Lieber-DeCarli alcohol liquid diet. We found that PGF administration significantly ameliorated alcohol-induced liver injury, steatosis, oxidative stress, and inflammation in mice. Furthermore, alcohol-increased levels of the critical hepatic lipid synthesis proteins sterol regulatory element binding transcription factor (SREBP-1) and diacylglycerol o-acyltransferase 2 (DGAT2) were attenuated by PGF. Similarly, PGF inhibited the expression of the lipid transport protein very lowdensity lipoprotein receptor (VLDLR). Interestingly, PGF restored alcohol-inhibited expression of carnitine palmitoyltransferase 1 (CPT1) and peroxisome proliferator-activated receptor alpha (PPAR alpha), essential fatty acid beta-oxidation proteins. Mechanistic studies revealed that PGF protects against alcohol-induced hepatocyte injury and lipid deposition via the SIRT1/AMPK signaling pathway. In sum, this research clearly demonstrated the protective effects of PGF against ALD, which was mediated by activating SIRT1/AMPK pathways in hepatocytes. We provide a new theoretical basis for using P. chinense as a functional food in ALD.
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页数:12
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