Effects of Hesperidin on the Progression of Hypercholesterolemia and Fatty Liver Induced by High-Cholesterol Diet in Rats

被引:90
作者
Wang, Xinhui [1 ]
Hasegawa, Junichi [1 ]
Kitamura, Yoshiyuki [1 ]
Wang, Zhongzhi [1 ]
Matsuda, Akiko [1 ]
Shinoda, Waka [1 ]
Miura, Norimasa [1 ]
Kimura, Koji [2 ]
机构
[1] Tottori Univ, Fac Med, Div Pharmacotherapeut, Dept Pathophysiol & Therapeut Sci, Yonago, Tottori 6838503, Japan
[2] Tottori Univ, Res Ctr Biosci & Technol, Div Funct Radiat Sci, Yonago, Tottori 6838503, Japan
关键词
hypercholesterolemia; hesperidin; fatty liver; lipid metabolism-related gene; RETINOID-BINDING PROTEIN; MESSENGER-RNA LEVELS; CITRUS FLAVONOIDS; SERUM-CHOLESTEROL; GENE-EXPRESSION; ACYL-COA; DISEASE; ATHEROSCLEROSIS; ABSORPTION; THERAPY;
D O I
10.1254/jphs.11097FP
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The protective effects of hesperidin against hypercholesterolemia and fatty liver were examined in male Wistar rats fed a high-cholesterol diet for 12 weeks. Compared with a standard diet, a high-cholesterol diet not only increased body weights, liver weights, and serum concentration of cholesterol, but also induced the fatty degeneration (steatosis) of liver. Hesperidin (0.08%) reduced levels of hepatic steatosis, adipose tissue and liver weights (P < 0.05), serum total cholesterol and retinol binding protein (RBP) 4 concentrations (P < 0.05) in rats fed with high-cholesterol diet, while reduction in low-density lipoprotein cholesterol levels and triglyceride concentrations was not significant. It also attenuated the marked changes in mRNA expression of lipid metabolism related proteins: RBP, heart fatty acid binding protein (H-FABP), and cutaneous fatty acid-binding protein (C-FABP), in liver and adipose tissue. According to the results of gas chromatography, serum concentrations of total cholesterol and biomarkers of cholesterol synthesis (lathosterol) and absorption (campesterol, beta-sitosterol) were lower, and concentrations of cholesterol in feces were higher in the rats given hesperidin (P < 0.05). Hesperidin may improve hypercholesterolemia and fatty liver by inhibiting both the synthesis and absorption of cholesterol and regulating the expression of mRNA for RBP, C-FABP, and H-FABP.
引用
收藏
页码:129 / 138
页数:10
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