Inhibitory effect of trans-tiliroside on very low-density lipoprotein secretion in HepG2 cells and mouse liver

被引:1
|
作者
Nagatomo, Akifumi [1 ,2 ]
Kohno, Mamiko [2 ]
Kawakami, Hirosato [2 ]
Manse, Yoshiaki [1 ]
Morikawa, Toshio [1 ,3 ]
机构
[1] Kindai Univ, Pharmaceut Res & Technol Inst, 3-4-1 Kowakae, Higashi Osaka, Osaka 5778502, Japan
[2] Morishita Jintan Co Ltd, 11-1 Tsudayamate 2 Chome, Hirakata, Osaka 5730128, Japan
[3] Kindai Univ, Antiaging Ctr, 3-4-1 Kowakae, Higashi Osaka, Osaka 5778502, Japan
关键词
Trans-tiliroside; Rose hip; Cholesterol; VLDL; Dyslipidemia; Apoprotein; TRIGLYCERIDE TRANSFER PROTEIN; GLUCOSYL HESPERIDIN; LIPID-METABOLISM; ROSE HIP; APO-B; FLAVONOIDS; DIET; RISK; ATHEROSCLEROSIS; HESPERETIN;
D O I
10.1007/s11418-023-01756-0
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An acylated flavonol glycoside, trans-tiliroside (1), is found in certain parts of different herbs, including the seeds of Rosa canina (Rosaceae). Previous studies on compound 1 have focused on triglyceride (TG) metabolism, including its anti-obesity and intracellular TG reduction effects. In the present study, the effects of compound 1 on cholesterol (CHO) metabolism were investigated using human hepatocellular carcinoma-derived HepG2 cells and mice. Compound 1 decreased CHO secretion in HepG2 cells, which was enhanced by mevalonate in a concentration-dependent manner and decreased the secretion of apoprotein B (apoB)-100, a marker of very low-density lipoprotein (VLDL). Compound 1 also inhibited the activity of microsomal triglyceride transfer proteins, which mediate VLDL formation from cholesterol and triglycerides in the liver. In vivo, compound 1 inhibited the accumulation of Triton WR-1339-induced TG in the blood of fasted mice and maintained low levels of apoB-100. These results suggest that compound 1 inhibits the secretion of CHO as VLDL from the liver and has the potential for use for the prevention of dyslipidemia.
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页码:180 / 190
页数:11
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