4.5 Article

Effect of Eclipta prostrata on lipid metabolism in hyperlipidemic animals

Journal

EXPERIMENTAL GERONTOLOGY
Volume 62, Issue -, Pages 37-44

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exger.2014.12.017

Keywords

Eclipta prostrata; Antioxidant; Hyperlipidemia; Triton WR-1339; HMG-CoA reductase

Funding

  1. Research Fund of Strait (Xiamen) Technology Platform in Traditional Chinese Medicine [3502Z20100006]

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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 studywas 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 HPD450 macroporous resin column chromatography of the EP, were screened in hyperlipidemic mice for lipidlowering activity, and EPF3 was the most active fraction. The LD50 of EPF3 was undetectable because no mice diedwith 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 metabolismin 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; upregulated the mRNA expression of peroxisome proliferator-activated receptor alpha (PPAR alpha), low density lipoprotein receptor (LDLR), lecithin-cholesterol transferase (LCAT) and scavenger receptor class B type. 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. (C) 2015 Elsevier Inc. All rights reserved.

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