Evaluation of hesperetin 7-O-lauryl ether as lipid-lowering agent in high-cholesterol-fed rats

被引:25
作者
Choi, GS
Lee, S
Jeong, TS
Lee, MK
Lee, JS
Jung, UJ
Kim, HJ
Park, YB
Bok, SH
Choi, MS
机构
[1] Kyungpook Natl Univ, Dept Food Sci & Nutr, Taegu 702701, South Korea
[2] Korea Res Inst Biosci & Biotechnol, Taejon 305333, South Korea
[3] Kyungpook Natl Univ, Food & Bioind Res Inst, Taegu 702701, South Korea
[4] Kyungpook Natl Univ, Dept Genet Engn, Taegu 702701, South Korea
关键词
hesperetin derivative; lipid lowering; HMG-CoA reductase; ACAT;
D O I
10.1016/j.bmc.2004.04.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The lipid-lowering efficacy of hesperetin was revealed in preliminary studies on experimental animals. As such, the current study compared the effect of hesperetin 7-O-lauryl ether, with that of hesperetin and lovastatin on the lipid profile and cholesterol-regulating mechanism in high-cholesterol-fed rats. Male rats were fed a high-cholesterol diet (1%, wt/wt) or high-cholesterol diet supplemented with lovastatin (1, 0.02%, wt/wt), hesperetin (2, 0.02%, wt/wt), or hesperetin 7-O-lauryl ether (3, 0.031%, wt/wt) for six weeks. The supplemental amount of 3 was 0.066 mmol/100 g diet as an equivalent to the supplemental amount of 2. The plasma total cholesterol and triglyceride levels were significantly lowered by the 2 and 3 supplements compared with the control or 1-supplemented group. The hepatic HMG-CoA reductase activities were also significantly lower in all the supplemented groups compared with the control group, and the hepatic ACAT activity was significantly lower in the 2- and 3-supplemented groups. The supplementation of 3 resulted in a higher excretion of total neutral sterol and total fecal sterol compared with the control or 1-supplemented group. Accordingly, overall, compound 3, exhibited a more potent plasma lipid-lowering effect than compound I based on inhibiting cholesterol biosynthesis and esterification, while also increasing the fecal sterol excretion. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3599 / 3605
页数:7
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