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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bioorganic & medicinal chemistry 2004-07, Vol.12 (13), p.3599-3605
Hauptverfasser: Choi, Gab-Sun, Lee, Sangku, Jeong, Tae-Sook, Lee, Mi-Kyung, Lee, Jeong-Sun, Jung, Un Ju, Kim, Hye-Jin, Park, Yong Bok, Bok, Song-Hae, Choi, Myung-Sook
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
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.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2004.04.020