The important role of glycerophospholipid metabolism in the protective effects of polyphenol-enriched Tartary buckwheat extract against alcoholic liver disease

被引:3
|
作者
Cao, Peng [1 ,2 ]
Wu, Yue [3 ]
Li, Yaping [4 ]
Xiang, Liping [1 ,2 ]
Cheng, Bingyu [4 ]
Hu, Yixin [4 ]
Jiang, Xin [4 ]
Wang, Zhe [3 ]
Wu, Sanlan [1 ,2 ]
Si, Luqin [4 ]
Yang, Qiang [3 ]
Xu, Jian [3 ]
Huang, Jiangeng [4 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Pharm, Wuhan 430022, Peoples R China
[2] Hubei Prov Clin Res Ctr Precis Med Crit Illness, Wuhan 430022, Peoples R China
[3] Jing Brand Co Ltd, Hubei Prov Key Lab Qual & Safety Tradit Chinese M, Jing Brand Res Inst, Daye 435100, Hubei, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Pharm, Dept Pharmaceut, Wuhan 430030, Peoples R China
基金
中国国家自然科学基金;
关键词
ACTIVATED PROTEIN-KINASE; OXIDATIVE STRESS; CELL-DEATH; IN-VIVO; MICE; RUTIN; ANTIOXIDANT; MODULATION; LIPIDOMICS; QUERCETIN;
D O I
10.1039/d2fo01518h
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
Alcoholic liver disease (ALD) is a mounting public health problem with significant medical, economic and social burdens. Tartary buckwheat (F. tataricum (L.) Gaertn, bitter buckwheat) is a kind of healthy and nutritious food, which has been demonstrated to protect against ALD, but the underlying mechanism has not been fully studied. Herein, we aimed to elucidate the beneficial effects of Tartary buckwheat extract (mainly composed of polyphenols including rutin, quercetin, kaempferol and kaempferol-3-O-rutinoside) in terms of lipid metabolism with the aid of lipidomic analysis. In our study, we employed C57BL/6J mice and a Lieber-DeCarli alcohol liquid diet to construct an ALD model and found that Tartary buckwheat extract was able to prevent ALD-induced histopathological lesions, liver injury and abnormal plasma lipid levels. These beneficial effects might be attributed to the regulation of energy metabolism-related genes (SIRT1, LKB1 and AMPK), lipid synthesis-related genes (ACC, SREBP1c and HMGR) and lipid oxidation-related genes (PPAR alpha, CPT1 and CPT2). In addition, lipidomic profiling and KEGG pathway analysis showed that glycerophospholipid metabolism contributed the most to elucidating the regulatory mechanism of Tartary buckwheat extract. In specific, chronic ethanol intake reduced the level of phosphatidylcholines (PC) and increased the level of phosphatidylethanolamines (PE) in the liver, resulting in a decrease in the PC/PE ratio, which could be all significantly restored by Tartary buckwheat extract intervention, indicating that the Tartary buckwheat extract might regulate PC/PE homeostasis to exert its lipid-lowering effect. Overall, we demonstrated that Tartary buckwheat extract could prevent ALD by modulating hepatic glycerophospholipid metabolism, providing the theoretical basis for its further exploitation as a medical plant or nutritional food.
引用
收藏
页码:10415 / 10425
页数:11
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