Eugeniin improves cholesterol metabolism in HepG2 cells and Caco-2 cells

被引:3
作者
Ye, Yuyang [1 ]
Takeuchi, Asahi [1 ]
Kawaguchi, Yuya [1 ]
Matsuba, Shoya [1 ]
Zhang, Ni [1 ]
Mijiti, Maihemuti [1 ]
Banno, Arata [1 ]
Hiramatsu, Naoto [2 ]
Okada, Toshitaka [2 ]
Nagaoka, Satoshi [1 ]
机构
[1] Gifu Univ, Fac Appl Biol Sci, Dept Appl Life Sci, Gifu, Japan
[2] Toyohakko Co Ltd, Dept Res & Dev, Obu, Aichi, Japan
关键词
eugeniin; LDL; HepG2; cells; cholesterol; Caco-2; HYPERCHOLESTEROLEMIA; ABSORPTION; HMGCR;
D O I
10.1093/bbb/zbad158
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
Considering the absence of prior studies on the cholesterol metabolism-improving effects of eugeniin, the present investigation aimed to explore the potential impact of eugeniin on cholesterol metabolism. This study sought to elucidate the molecular mechanisms involved in this process using HepG2 and Caco-2 cells treated with 5 mu m eugeniin. The intracellular cholesterol levels in HepG2 and Caco-2 cells were significantly decreased in the 24-h eugeniin-treated group. The protein and messenger ribonucleic acid (mRNA) levels of the low-density lipoprotein receptor (LDLR) were increased, while 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase protein and mRNA levels were decreased in HepG2 cells 6 h of the eugeniin-treated group. Additionally, LDLR protein and mRNA levels were increased in HepG2 cells after 24 h of eugeniin treatment. In Caco-2, the protein and mRNA levels of ATP-binding cassette transporter 1 were increased after 24 h eugeniin treatment. This novel finding indicates that eugeniin improves cholesterol metabolism in human cell cultures. Graphical Abstract Mechanism of action to improve cholesterol metabolism by eugeniin in HepG2 cells and Caco-2 cells.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 31 条
[1]   Identification of a novel cholesterol-lowering dipeptide, phenylalanine-proline (FP), and its down-regulation of intestinal ABCA1 in hypercholesterolemic rats and Caco-2 cells [J].
Banno, Arata ;
Wang, Jilite ;
Okada, Kenji ;
Mori, Ryosuke ;
Mijiti, Maihemuti ;
Nagaoka, Satoshi .
SCIENTIFIC REPORTS, 2019, 9 (1)
[2]   Modifying pH-sensitive PCSK9/LDLR interactions as a strategy to enhance hepatic cell uptake of low-density lipoprotein cholesterol (LDL-C) [J].
Ben-Naim, Lital ;
Khalaila, Isam ;
Papo, Niv .
PROTEIN ENGINEERING DESIGN & SELECTION, 2022, 35
[3]   NPC1L1 and cholesterol transport [J].
Betters, Jenna L. ;
Yu, Liqing .
FEBS LETTERS, 2010, 584 (13) :2740-2747
[4]   Tellimagrandin II, A Type of Plant Polyphenol Extracted from Trapa bispinosa Inhibits Antibiotic Resistance of Drug-Resistant Staphylococcus aureus [J].
Chang, Yu-Wei ;
Huang, Wan-Chun ;
Lin, Chun-Yu ;
Wang, Wen-Hung ;
Hung, Ling-Chien ;
Chen, Yen-Hsu .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (22)
[5]   Developmental processes regulated by the 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) pathway: Highlights from animal studies [J].
Eisa-Beygi, Shahram ;
Ekker, Marc ;
Moon, Thomas W. ;
Macdonald, R. Loch ;
Wen, Xiao-Yan .
REPRODUCTIVE TOXICOLOGY, 2014, 46 :115-120
[6]   Curcumin inhibits cholesterol uptake in Caco-2 cells by down-regulation of NPC1L1 expression [J].
Feng, Dan ;
Ohlsson, Lena ;
Duan, Rui-Dong .
LIPIDS IN HEALTH AND DISEASE, 2010, 9
[7]   Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR [J].
Galicia-Garcia, Unai ;
Benito-Vicente, Asier ;
Uribe, Kepa B. ;
Jebari, Shifa ;
Larrea-Sebal, Asier ;
Alonso-Estrada, Rocio ;
Aguilo-Arce, Joseba ;
Ostolaza, Helena ;
Palacios, Lourdes ;
Martin, Cesar .
SCIENTIFIC REPORTS, 2020, 10 (01) :1727
[8]   Molecular medicine - The cholesterol quartet [J].
Goldstein, JL ;
Brown, MS .
SCIENCE, 2001, 292 (5520) :1310-1312
[9]   A Century of Cholesterol and Coronaries: From Plaques to Genes to Statins [J].
Goldstein, Joseph L. ;
Brown, Michael S. .
CELL, 2015, 161 (01) :161-172
[10]   Lipid Absorption Defects in Intestine-specific Microsomal Triglyceride Transfer Protein and ATP-binding Cassette Transporter A1-deficient Mice [J].
Iqbal, Jahangir ;
Parks, John S. ;
Hussain, M. Mahmood .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (42) :30432-30444