Evaluation of hesperetin 7- O-lauryl ether as lipid-lowering agent in high-cholesterol-fed rats
This study examined the lipid-lowering effect of hesperetin 7- O-lauryl ether in high-cholesterol-fed rats. The supplementation of this compound was effective in altering lipid metabolism and lowering plasma cholesterol level. The lipid-lowering efficacy of hesperetin was revealed in preliminary stu...
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Veröffentlicht in: | Bioorganic & medicinal chemistry 2004-07, Vol.12 (13), p.3599-3605 |
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Sprache: | eng |
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Zusammenfassung: | This study examined the lipid-lowering effect of hesperetin 7-
O-lauryl ether in high-cholesterol-fed rats. The supplementation of this compound was effective in altering lipid metabolism and lowering plasma cholesterol level.
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
1 based on inhibiting cholesterol biosynthesis and esterification, while also increasing the fecal sterol excretion. |
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ISSN: | 0968-0896 1464-3391 |
DOI: | 10.1016/j.bmc.2004.04.020 |