Antiatherogenicity of extra virgin olive oil and its enrichment with green tea polyphenols in the atherosclerotic apolipoprotein-E-deficient mice: enhanced macrophage cholesterol efflux

被引:63
作者
Rosenblat, Mira [1 ]
Volkova, Nina [1 ]
Coleman, Raymond [2 ]
Almagor, Yaron [3 ]
Aviram, Michael [1 ]
机构
[1] Rambam Med Ctr, Lipid Res Lab, Technion Fac Med, Rappaport Family Inst Res Med Sci, IL-31096 Haifa, Israel
[2] Technion Fac Med, Dept Anat & Cell Biol, IL-31096 Haifa, Israel
[3] Shaare Zedek Med Ctr, Dept Cardiol, IL-91031 Jerusalem, Israel
关键词
olive oil; green tea polyphenols; macrophages; oxidative stress; atherosclerosis;
D O I
10.1016/j.jnutbio.2007.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The antiatherogenic properties of extra virgin olive oil (EVOO) enriched with green tea polyphenols (GTPPs; hereafter called EVOO-GTPP), in comparison to EVOO, were studied in the atherosclerotic apolipoprotein-E-deficient (E) mice. Eo mice (eight mice in each group) consumed EVOO or EVOO-GTPP (7 mu l/mouse/day, for 2 months) by gavage feeding. The placebo group received only water. At the end of the study, blood samples, peritoneal macrophages and aortas were collected. Consumption of EVOO or EVOO-GTPP resulted in a minimal increase in serum total and high-density lipoprotein (HDL) cholesterol levels (by 12%) and in serum paraoxonase 1 activity (by 6% and 10%). EVOO-GTPP (but not EVOO) decreased the susceptibility of the mouse serum to AAPH-induced lipid peroxidation (by 18%), as compared to the placebo-treated mice. The major effect of both EVOO and EVOO-GTPP consumption was on HDL-mediated macrophage cholesterol efflux. Consumption of EVOO stimulated cholesterol efflux rate from mouse peritoneal macrophages (MPMs) by 42%, while EVOO-GTPP increased it by as much as 139%, as compared to MPMs from placebo-treated mice. Finally, the atherosclerotic lesion size of mice was significantly reduced by 11% or 20%, after consumption of EVOO or EVOO-GTPP, respectively. We thus conclude that EVOO possesses beneficial antiatherogenic effects, and its enrichment with GTPPs further improved these effects, leading to the attenuation of atherosclerosis development. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:514 / 523
页数:10
相关论文
共 70 条
[1]   Dietary cholesterol suppresses the ability of olive oil to delay the development of atherosclerotic lesions in apolipoprotein E knockout mice [J].
Acín, S ;
Navarro, MA ;
Carnicer, R ;
Arbonés-Mainar, JM ;
Guzmán, MA ;
Arnal, C ;
Beltrán, G ;
Uceda, M ;
Maeda, N ;
Osada, J .
ATHEROSCLEROSIS, 2005, 182 (01) :17-28
[2]   Olive oil preparation determines the atherosclerotic protection in apolipoprotein E knockout mice [J].
Acin, Sergio ;
Navarro, Maria A. ;
Perona, Javier S. ;
Arbones-Mainar, Jose M. ;
Surra, Joaquin C. ;
Guzman, Mario A. ;
Carnicer, Ricardo ;
Arnal, Carmen ;
Orman, Israel ;
Segovia, Jose C. ;
Osada, Jesus ;
Ruiz-Gutierrez, Valentina .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2007, 18 (06) :418-424
[3]   Sunflower, virgin-olive and fish oils differentially affect the progression of aortic lesions in rabbits with experimental atherosclerosis [J].
Aguilera, CM ;
Ramírez-Tortosa, MC ;
Mesa, MD ;
Ramírez-Tortosa, CL ;
Gil, A .
ATHEROSCLEROSIS, 2002, 162 (02) :335-344
[4]  
Andrikopoulos Nikolaos K., 2002, Journal of Medicinal Food, V5, P1, DOI 10.1089/109662002753723160
[5]   DIETARY OLIVE OIL REDUCES LOW-DENSITY-LIPOPROTEIN UPTAKE BY MACROPHAGES AND DECREASES THE SUSCEPTIBILITY OF THE LIPOPROTEIN TO UNDERGO LIPID-PEROXIDATION [J].
AVIRAM, M ;
EIAS, K .
ANNALS OF NUTRITION AND METABOLISM, 1993, 37 (02) :75-84
[6]   PLASMA-LIPOPROTEIN SEPARATION BY DISCONTINUOUS DENSITY GRADIENT ULTRA-CENTRIFUGATION IN HYPERLIPOPROTEINEMIC PATIENTS [J].
AVIRAM, M .
BIOCHEMICAL MEDICINE, 1983, 30 (01) :111-118
[7]   Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions - A possible peroxidative role for paraoxonase [J].
Aviram, M ;
Rosenblat, M ;
Bisgaier, CL ;
Newton, RS ;
Primo-Parmo, SL ;
La Du, BN .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (08) :1581-1590
[8]  
Aviram M, 2000, AM J CLIN NUTR, V71, P1062
[9]  
AVIRAM M, 1994, J LIPID RES, V35, P385
[10]  
AVIRAM M, 2003, OXIDATIVE STRESS CAR, P557