Sea Buckthorn Polyphenols Alleviate High-Fat-Diet-Induced Metabolic Disorders in Mice via Reprograming Hepatic Lipid Homeostasis Owing to Directly Targeting Fatty Acid Synthase

被引:3
|
作者
Yuan, Luping [1 ]
Zhang, Wanlin [1 ]
Fang, Wenxiu [1 ]
Zhuang, Xinying [1 ]
Gong, Wan [2 ]
Xu, Xiaoying [3 ]
Li, Yingting [1 ]
Wang, Xiaoyan [1 ]
机构
[1] Zhejiang Chinese Med Univ, Sch Pharmaceut Sci, Hangzhou 311402, Peoples R China
[2] Zhejiang Chinese Med Univ, Fuyang Res Inst, Hangzhou 310053, Peoples R China
[3] Zhejiang Chinese Med Univ, Sch Basic Med Sci, Hangzhou 310053, Peoples R China
基金
中国国家自然科学基金;
关键词
excess energy intake; lipotoxicity; targetedquantitative lipidomics; lipid-based biomarker; functional food; target enzyme; intermolecularinteractions; binding affinity; INSULIN-RESISTANCE; BODY-WEIGHT; LIVER; OBESITY; THIOESTERASE; LIPOGENESIS; STEATOSIS; PLASMA; ISSUES; NAFLD;
D O I
10.1021/acs.jafc.4c01351
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Our previous studies found that Sea Buckthorn polyphenols (SBP) extract inhibits fatty acid synthase (FAS) in vitro. Thus, we continued to explore possible effects and underlying mechanisms of SBP on complicated metabolic disorders in long-term high-fat-diet (HFD)-fed mice. To reveal that, an integrated approach was developed in this study. Targeted quantitative lipidomics with a total of 904 unique lipids mapping contributes to profiling the comprehensive features of disarranged hepatic lipid homeostasis and discovering a set of newfound lipid-based biomarkers to predict the occurrence and indicate the progression of metabolic disorders beyond current indicators. On the other hand, technologies of intermolecular interactions characterization, especially surface plasmon resonance (SPR) assay, contribute to recognizing targeted bioactive constituents present in SBP. Our findings highlight hepatic lipid homeostasis maintenance and constituent-FAS enzyme interactions, to provide new insights that SBP as a functional food alleviates HFD-induced metabolic disorders in mice via reprograming hepatic lipid homeostasis caused by targeting FAS, owing to four polyphenols directly interacting with FAS and cinaroside binding to FAS with good affinity.
引用
收藏
页码:8632 / 8649
页数:18
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