Hypolipidaemic activity of dimethoxy unconjugated propenyl side-chain analogs of α-asarone in mice

被引:0
|
作者
Chamorro, G
Garduño, L
Sánchez, A
Labarrios, F
Salazar, M
Martínez, E
Díaz, F
Tamariz, J
机构
[1] Natl Polytech Inst, Natl Sch Biol Sci, Dept Toxicol, Mexico City 11591, DF, Mexico
[2] Natl Polytech Inst, Natl Sch Biol Sci, Dept Chem, Mexico City 11591, DF, Mexico
关键词
alpha-asarone; hypolipidaemia; hypocholesterolaemia; lipid lowering;
D O I
10.1002/(SICI)1098-2299(199802)43:2<105::AID-DDR3>3.0.CO;2-O
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The hypolipidaemic activity of several dimethoxy unconjugated propenyl side-chain analogs of alpha-asarone were investigated in hyperlipidaemic mice after six days of treatment. Eugenol and the alpha-asarone analog with amino groups on the C-4 position of the aromatic ring were observed to be the most effective hypolipidaemic agents at the dose of 80 mg/kg/day p.o. These compounds significantly lowered total serum cholesterol, low density lipoprotein (LDL-cholesterol), and triglycerides content. On the other hand, high density lipoprotein (HDL-cholesterol) was increased by administration of these hypolipidaemic agents. The ability to modulate the levels of these lipids suggests that these agents could be effective in the treatment of hyperlipidaemic states. These compounds appeared to be safe when administered at an oral dose of 80 mg/kg/day, which is within the therapeutic range in mice. (C) 1998 Wiley-Liss, Inc.
引用
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页码:105 / 108
页数:4
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