4.5 Article

Combination of spices and herbal extract restores macrophage foam cell migration and abrogates the athero-inflammatory signalling cascade of atherogenesis

Journal

VASCULAR PHARMACOLOGY
Volume 72, Issue -, Pages 53-63

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.vph.2015.02.014

Keywords

Album sativum; Terminalia arjuna; Anti-atherosclerotic; Macrophages foam cell; Polyphenols

Funding

  1. National Institute of Nutrition
  2. Indian Council of Medical Research
  3. Department of Health Research, Ministry Health and family welfare, Govt. of India, Hyderabad

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The trapping of lipid-laden macrophages in the arterial intima is a critical but reversible step in atherogenesis. However, information about possible treatments for this condition is lacking. Here, we hypothesized that combining the polyphenol-rich fractions (PHC) of commonly consumed spices (Allium sativum L (Liliaceae), Zingiber officinale R (Zingiberaceae), Curcuma longa L (Zingiberaceae)) and herbs (Terminalia arjuna (R) W & A (Combretaceae) and Cyperus rotundus L (Cyperaceae)) prevents foam cell formation and atherogenesis. Using an in vitro foam cell formation assay, we found that PHC significantly inhibited lipid-laden macrophage foam cell formation compared to the depleted polyphenol fraction of PHC (F-PHC). We further observed that PHC attenuated the LDL and LPS induced CD36, p-FAK and PPAR-gamma protein expression in macrophages and increased their migration. NK-kappa B-DNA interaction, TNF-alpha, ROS generation, and MMP9 and MMP2 protein expression were suppressed in PHC-treated macrophages. The anti-atherosclerotic activity of PHC was investigated in a high fat- and cholesterol-fed rabbit model. The inhibition of foam cell deposition within the aortic intima and atheroma formation confirmed the atheroprotective activity of PHC Therefore, we conclude that the armoury of polyphenols in PHC attenuates the CD36 signalling cascade-mediated foam cell formation, enhances the migration of these cells and prevents atherogenesis. (C) 2015 Elsevier Inc. All rights reserved.

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