Interactive effect of hesperidin and vitamin E supplements on cholesterol metabolism in high cholesterol-fed rats

被引:31
作者
Park, YB
Do, KM
Bok, SH
Lee, MK
Jeong, TS
Choi, MS
机构
[1] Kyungpook Natl Univ, Dept Nutr & Food Sci, Puk Ku, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Dept Genet Engn, Puk Ku, Taegu 702701, South Korea
[3] KIST, Korea Inst Biosci & Biotechnol, Taejon 305606, South Korea
关键词
hesperidin; vitamin E; HMG-CoA reductase; ACAT; fecal sterols; cholesterol metabolism; antioxidant enzymes;
D O I
10.1024/0300-9831.71.1.36
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Certain bioflavonoids are potent antioxidants and have pharmacologic effects similar to those of vitamin E. Accordingly, the interactive effect of hesperidin and vitamin E was studied with respect to cholesterol metabolism and the antioxidant status. Hesperidin supplement (0.1%. wt/wt) with comparable levels of vitamin E was provided with a high-cholesterol (1%, wt/wt) diet to rats fur 5 weeks. The amount of vitamin E included in the:hesperidin-free and hesperidin diets was either a low (low-E) or a normal (normal-E) level. The : hesperidin supplement and different levels of dietary vitamin E did not significantly alter the concentrations of plasma triglycerides. However, the inclusion of hesperidin significantly lowered the concentration of plasma cholesterol in both the low-vitamin E group and the normal-vitamin E group compared to the hesperidin-free groups (p < 0.05). The hepatic triglyceride content was significantly lowered by the hesperidin supplement, as opposed to the plasma triglyceride content, regardless of the vitamin E level in the diet. The hepatic HMG-CoA reductase activity was significantly lowered by the hesperidin supplement with both the low-vitamin E and the normal-vitamin E compared to the hesperidin-free groups (p < 0.05). The hepatic HMG-CoA reductase activity was also significantly lowered with an increase in the dietary vitamin E within the hesperidin and hesperidin-free groups. The excretion of fecal neutral sterol and acidic sterols tended to be lower with the hesperidin supplement. Neither dietary hesperidin nor vitamin E significantly changed the hepatic antioxidant enzyme activity. This data indicates that hesperidin lowers the concentration of plasma cholesterol and the hepatic triglyceride content regardless of the dietary vitamin E level. However, the concentration of plasma cholesterol in the hesperidin-free groups was dependent on the dietary vitamin E level. This information may contribute to understanding the interactive effect of hesperidin and vitamin E on cholesterol biosynthesis in high cholesterol-fed rats.
引用
收藏
页码:36 / 44
页数:9
相关论文
共 38 条
[1]  
Aboobaker V S, 1994, In Vivo, V8, P1095
[2]  
Aebi H., 1974, Methods in Enzymatic Analysis, V2, P674, DOI [DOI 10.1016/B978-0-12-091302-2.50032-3, 10.1016/B978-0-12-091302-2.50032-3]
[3]  
ALLAIN CC, 1974, CLIN CHEM, V20, P470
[4]   Flavanone absorption after naringin, hesperidin, and citrus administration [J].
Ameer, B ;
Weintraub, RA ;
Johnson, JV ;
Yost, RA ;
Rouseff, RL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 60 (01) :34-40
[5]  
[Anonymous], 1995, NUTRIENT REQUIREMENT, V4th, P11, DOI DOI 10.17226/4758
[6]  
[Anonymous], J NUTR
[7]   SIMULTANEOUS DETERMINATION OF ALPHA-TOCOPHEROL AND RETINOL IN PLASMA OR RED-CELLS BY HIGH-PRESSURE LIQUID-CHROMATOGRAPHY [J].
BIERI, JG ;
TOLLIVER, TJ ;
CATIGNANI, GL .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1979, 32 (10) :2143-2149
[8]  
BJORKHEM I, 1985, NEW COMPREHENSIVE BI, P231
[9]   HMG-CoA reductase and ACAT inhibitors act synergistically to lower plasma cholesterol and limit atherosclerotic lesion development in the cholesterol-fed rabbit [J].
Bocan, TMA ;
Mueller, SB ;
Brown, EQ ;
Lee, P ;
Bocan, MJ ;
Rea, T ;
Pape, ME .
ATHEROSCLEROSIS, 1998, 139 (01) :21-30
[10]   Plasma and hepatic cholesterol and hepatic activities of 3-hydroxy-3-methyl-glutaryl-CoA reductase and acyl CoA: Cholesterol transferase are lower in rats fed citrus peel extract or a mixture of citrus bioflavonoids [J].
Bok, SH ;
Lee, SH ;
Park, YB ;
Bae, KH ;
Son, KH ;
Jeong, TS ;
Choi, MS .
JOURNAL OF NUTRITION, 1999, 129 (06) :1182-1185