Naringin, the major grapefruit flavonoid, specifically affects atherosclerosis development in diet-induced hypercholesterolemia in mice

被引:160
作者
Chanet, Audrey [1 ,2 ]
Milenkovic, Dragan [1 ,2 ]
Deval, Christiane [1 ,2 ]
Potier, Mylene [3 ]
Constans, Joel [4 ]
Mazur, Andrzej [1 ,2 ]
Bennetau-Pelissero, Catherine [3 ]
Morand, Christine [1 ,2 ]
Berard, Annie M. [4 ]
机构
[1] INRA, UMR 1019, UNH, CRNH Auvergne, F-63000 Clermont Ferrand, France
[2] Univ Clermont Ferrand, Univ Auvergne, Unite Nutr Humaine, F-63000 Clermont Ferrand, France
[3] Univ Bordeaux, ENITA Bordeaux 1, F-33175 Gradignan, France
[4] CHU Univ Bordeaux, ERU Facteurs Risque Vasc, F-33076 Bordeaux, France
关键词
Naringin; Flavonoid; Atherosclerosis; High-fat high-cholesterol diet; Hypercholesterolemic mouse models; Transcriptomic; SMOOTH-MUSCLE-CELLS; DENSITY-LIPOPROTEIN RECEPTOR; VASCULAR ENDOTHELIAL-CELLS; CORONARY-HEART-DISEASE; MESSENGER-RNA LEVELS; HEPATOCYTE APO-B; CITRUS FLAVONOIDS; ADHESION MOLECULE-1; INSULIN-RECEPTOR; KNOCKOUT MICE;
D O I
10.1016/j.jnutbio.2011.02.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Naringin (NAR) from grapefruit has exhibited potential protective effects against atherosclerosis development However, specific mechanisms responsible for such effects are poorly understood. Thus, we aimed to investigate the antiatherogenic effects of NAR in different mouse models of hypercholesterolemia and decipher its molecular targets in the aorta using transcriptomic approach. Two mouse models of hypercholesterolemia, wild-type mice fed a high-fat/high-cholesterol diet and apolipoprotein E-deficient mice fed a semisynthetic diet, were studied. Mice were fed a respective control diets supplemented or not for 18 weeks with 0.02% of NAR, that is, nutritional supplementation. NAR supplementation reduced plaque progression only in wild-type mice fed the high-fat/high-cholesterol diet (-41%). Consistent with this protective effect, NAR reduced plasma non-high-density lipoprotein cholesterol concentrations as well as biomarkers of endothelial dysfunction. Microarray studies performed on aortas demonstrated differentially expressed genes encoding proteins involved in cell adhesion, actin cytoskeleton organization and cell division. Thus, the changes in gene expression induced by NAR could suggest a limited atherosclerosis progression by preventing immune cell adhesion and infiltration in the intima of vascular wall, as well as smooth muscle cell proliferation. Furthermore, this hypothesis was strengthened by in vitro experiments, which showed the ability of naringenin to reduce monocyte adhesion to endothelial cells and smooth muscle cell proliferation. In conclusion, this study revealed the antiatherogenic effect of NAR supplemented at a nutritionally achievable dose, specifically toward diet-induced atherosclerosis, and depicted its multitarget mode of action at the vascular level. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:469 / 477
页数:9
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