Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient mice

<p>Abstract</p> <p>The present study was performed to investigate the effects of the combination therapy of pinocembrin and simvastatin on the atherosclerotic lesions development in the ApoE<sup>−/−</sup> mice.</p> <p>Methods</p> <p>Eight-week-ol...

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Main Authors: Sang Hui, Yuan Na, Yao Shutong, Li Furong, Wang Jiafu, Fang Yongqi, Qin Shucun
Format: Article
Language:English
Published: BMC 2012-12-01
Series:Lipids in Health and Disease
Subjects:
Online Access:http://www.lipidworld.com/content/11/1/166
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author Sang Hui
Yuan Na
Yao Shutong
Li Furong
Wang Jiafu
Fang Yongqi
Qin Shucun
author_facet Sang Hui
Yuan Na
Yao Shutong
Li Furong
Wang Jiafu
Fang Yongqi
Qin Shucun
author_sort Sang Hui
collection DOAJ
description <p>Abstract</p> <p>The present study was performed to investigate the effects of the combination therapy of pinocembrin and simvastatin on the atherosclerotic lesions development in the ApoE<sup>−/−</sup> mice.</p> <p>Methods</p> <p>Eight-week-old male ApoE<sup>−/−</sup> mice were fed high fat diet (HFD) and treated with simvastatin (10 mg/kg per day), pinocembrin (20 mg/kg per day), or the combination therapy (simvastatin 5 mg/kg per day and pinocembrin 20 mg/kg per day) for 14 weeks. The serum lipid levels, nitric oxide (NO), endothelin (ET), superoxide dismutase (SOD) and malondialdehyde (MDA) were determined with spectrophotometric measurement and ELISA assay. Vascular endothelial growth factor (VEGF) in serum and aortic root was detected. En face analyses of atherosclerotic lesion in whole aorta and aortic root sections were performed with plaque staining using oil red O.</p> <p>Results</p> <p>The combination treatment with simvastatin and pinocembrin resulted in significantly decreased levels of serum total cholesterol, triglycerides and low-density lipoprotein cholesterol, augmented NO levels and SOD activity, inhibited ET and VEGF expression. Immunohistochemistry of aortic valve sections revealed that the combination therapy also suppressed the expression of VEGF induced by HFD. In addition, HFD-induced arterial wall lipid disposition displayed by oil red O staining was reduced significantly in aortic root and whole aorta en face in the combination administrated mice. The effect of the combination was superior to simvastatin alone.</p> <p>Conclusion</p> <p>The combination of simvastatin and pinocembrin synergistically inhibited atherosclerotic lesion development in ApoE<sup>−/−</sup> mice with hyperlipidemia, which is partially dependent on the protective of vascular endothelium.</p>
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spelling doaj.art-1f37b99db5254d44a4991182815885b82022-12-21T22:01:33ZengBMCLipids in Health and Disease1476-511X2012-12-0111116610.1186/1476-511X-11-166Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient miceSang HuiYuan NaYao ShutongLi FurongWang JiafuFang YongqiQin Shucun<p>Abstract</p> <p>The present study was performed to investigate the effects of the combination therapy of pinocembrin and simvastatin on the atherosclerotic lesions development in the ApoE<sup>−/−</sup> mice.</p> <p>Methods</p> <p>Eight-week-old male ApoE<sup>−/−</sup> mice were fed high fat diet (HFD) and treated with simvastatin (10 mg/kg per day), pinocembrin (20 mg/kg per day), or the combination therapy (simvastatin 5 mg/kg per day and pinocembrin 20 mg/kg per day) for 14 weeks. The serum lipid levels, nitric oxide (NO), endothelin (ET), superoxide dismutase (SOD) and malondialdehyde (MDA) were determined with spectrophotometric measurement and ELISA assay. Vascular endothelial growth factor (VEGF) in serum and aortic root was detected. En face analyses of atherosclerotic lesion in whole aorta and aortic root sections were performed with plaque staining using oil red O.</p> <p>Results</p> <p>The combination treatment with simvastatin and pinocembrin resulted in significantly decreased levels of serum total cholesterol, triglycerides and low-density lipoprotein cholesterol, augmented NO levels and SOD activity, inhibited ET and VEGF expression. Immunohistochemistry of aortic valve sections revealed that the combination therapy also suppressed the expression of VEGF induced by HFD. In addition, HFD-induced arterial wall lipid disposition displayed by oil red O staining was reduced significantly in aortic root and whole aorta en face in the combination administrated mice. The effect of the combination was superior to simvastatin alone.</p> <p>Conclusion</p> <p>The combination of simvastatin and pinocembrin synergistically inhibited atherosclerotic lesion development in ApoE<sup>−/−</sup> mice with hyperlipidemia, which is partially dependent on the protective of vascular endothelium.</p>http://www.lipidworld.com/content/11/1/166PinocembrinSimvastatinCombined therapyAtherosclerotic lesionApolipoprotein E knockout mice
spellingShingle Sang Hui
Yuan Na
Yao Shutong
Li Furong
Wang Jiafu
Fang Yongqi
Qin Shucun
Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient mice
Lipids in Health and Disease
Pinocembrin
Simvastatin
Combined therapy
Atherosclerotic lesion
Apolipoprotein E knockout mice
title Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient mice
title_full Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient mice
title_fullStr Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient mice
title_full_unstemmed Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient mice
title_short Inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoE-deficient mice
title_sort inhibitory effect of the combination therapy of simvastatin and pinocembrin on atherosclerosis in apoe deficient mice
topic Pinocembrin
Simvastatin
Combined therapy
Atherosclerotic lesion
Apolipoprotein E knockout mice
url http://www.lipidworld.com/content/11/1/166
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