Effect of Eclipta prostrata on lipid metabolism in hyperlipidemic animals

高脂血症 脂质代谢 内分泌学 内科学 清道夫受体 化学 过氧化物酶体增殖物激活受体 受体 作用机理 吉非罗齐 胆固醇 抗氧化剂 低密度脂蛋白受体 载脂蛋白B 药理学 生物 脂蛋白 生物化学 医学 糖尿病 体外
作者
Yun Zhao,Peng Lu,Wei Lü,Yiqing Wang,Xuefeng Huang,Chen Gong,Lin He,Junhao Hong,Songsong Wu,Xin Jin
出处
期刊:Experimental Gerontology [Elsevier BV]
卷期号:62: 37-44 被引量:35
标识
DOI:10.1016/j.exger.2014.12.017
摘要

Eclipta prostrata (Linn.) Linn. is a traditional Chinese medicine and has previously been reported to have hypolipidemic effects. However, its mechanism of action is not well understood. This study was conducted to identify the active fraction of Eclipta, its toxicity, its effect on hyperlipidemia, and its mechanism of action. The ethanol extract (EP) of Eclipta and fractions EPF1–EPF4, obtained by eluting with different concentrations of ethanol from a HPD-450 macroporous resin column chromatography of the EP, were screened in hyperlipidemic mice for lipid-lowering activity, and EPF3 was the most active fraction. The LD50 of EPF3 was undetectable because no mice died with administration of EPF3 at 10.4 g/kg. Then, 48 male hamsters were used and randomly assigned to normal chow diet, high-fat diet, high-fat diet with Xuezhikang (positive control) or EPF3 (75, 150 and 250 mg/kg) groups. We evaluated the effects of EPF3 on body weight gain, liver weight gain, serum lipid concentration, antioxidant enzyme activity, and the expression of genes involved in lipid metabolism in hyperlipidemic hamsters. The results showed that EPF3 significantly decreased body-weight gain and liver-weight gain and reduced the serum lipid levels in hyperlipidemic hamsters. EPF3 also increased the activities of antioxidant enzymes; up-regulated the mRNA expression of peroxisome proliferator-activated receptor α (PPARα), low density lipoprotein receptor (LDLR), lecithin-cholesterol transferase (LCAT) and scavenger receptor class B type Ι receptor (SR-BI); and down-regulated the mRNA expression of 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMGR) in the liver. These results indicate that EPF3 ameliorates hyperlipidemia, in part, by reducing oxidative stress and modulating the transcription of genes involved in lipid metabolism.
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