The Journal of Nutritional Biochemistry
Volume 21, Issue 4 , Pages 255-260, April 2010

Mechanisms of anti-atherosclerotic functions of soy-based diets

Department of Microbiology and Immunology, Arkansas Children's Nutrition Center, University of Arkansas for Medical Sciences, Little Rock, AR 72202, USA

Received 12 February 2009; received in revised form 17 July 2009; accepted 3 September 2009. published online 02 December 2009.

Abstract 

Soy-based diets have been reported to protect against the development of atherosclerosis. However, the underlying mechanism(s) for this protection remains unknown. Although atherosclerosis was traditionally considered a disease associated with impaired lipid metabolism, in recent years the inflammatory components of atherosclerosis have been explored. Recent studies have convincingly delineated that uncontrolled chronic inflammation is the principal contributing factor for the initiation and progression of atherosclerosis. Interaction between activated monocytes and vascular endothelial cells is an early event in atherogenesis. The adhesion of leukocytes, including monocytes, to the inflamed-vascular endothelium and their transmigration into intima initiate the inflammatory processes. Following transmigration, monocytes in the intima are transformed to macrophages, which take up oxidized-LDL (oxLDL) to generate lipid-laden macrophages, also known as foam cells. Hence, in this review article the inflammatory processes associated with atherosclerosis and possible anti-inflammatory functions of soy-based diets contributing to the prevention of atherosclerosis are presented.

Abbreviations: ApoE−/−, apolipoprotein E knockout, CD54, intercellular adhesion molecule-1, CD62E, E-selectin, CD62P, P-selectin, CD106, vascular cell adhesion molecule-1, CVD, cardiovascular disease, LDL, low-density lipoprotein, MCP-1, monocyte chemoattractant protein-1, oxLDL, oxidized-LDL, PPAR, peroxisome proliferator-activated receptor, TF, tissue factor

Keywords: Soy, Atherosclerosis, Isoflavones, Inflammation, Cell adhesion

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 This work was supported by a grant from USDA (CRIS 6251-51000-005-00D) (SN).

PII: S0955-2863(09)00193-4

doi:10.1016/j.jnutbio.2009.09.002

The Journal of Nutritional Biochemistry
Volume 21, Issue 4 , Pages 255-260, April 2010