Hydroxytyrosol administration enhances atherosclerotic lesion development in apo E deficient mice

被引:64
作者
Acin, Sergio
Navarro, Maria A.
Arbones-Mainar, Jose M.
Guillen, Natalia
Sarria, Alfonso J.
Carnicer, Ricardo
Surra, Joaquin C.
Orman, Israel
Segovia, Jose C.
de la Torre, Rafael
Covas, Maria-Isabel
Fernandez-Bolanos, Juan
Ruiz-Gutierrez, Valentina
Osada, Jesus
机构
[1] Univ Zaragoza, Dept Biochem & Mol Biol, Sch Vet, E-50013 Zaragoza, Spain
[2] CEIMAT, Dept Terapia Gen Hematopoyesis, Madrid, Spain
[3] Inst Municipal Invest Med Barcelona, Barcelona, Spain
[4] Inst Grasa, Seville, Spain
关键词
atherosclerosis; hydroxytyrosol; lipoproteins; olive oil; transgenic animal;
D O I
10.1093/jb/mvj166
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
Hydroxytyrosol is a phenol found in olive oil. To verify the effect of hydroxytyrosol on the development of atherosclerosis, two groups of apo E deficient male mice on a standard chow diet were used: the control group receiving only water, and the second group an aqueous solution of hydroxytyrosol in order to provide a dose of 10 mg/kg/day to each mouse. This treatment was maintained for 10 weeks. At the moment of sacrifice, blood was drawn and heart removed. Plasma lipids, apolipoproteins and monocyte Mac-1 expression were assayed as well as aortic atherosclerotic areas in both groups. Data showed no significant changes in HDL cholesterol, paraoxonase, apolipoprotein B or triglyceride levels. However, hydroxytyrosol administration decreased apolipoprotein A-I and increased total cholesterol, atherosclerotic lesion areas and circulating monocytes expressing Mac-1. The latter was highly correlated with lesion areas (r = 0.65, P < 0.01). These results indicate that administration of hydroxytyrosol in low cholesterol diets increases atherosclerotic lesion associated with the degree of monocyte activation and remodelling of plasma lipoproteins. Our data supports the concept that phenolic-enriched products, out of the original matrix, could be not only non useful but also harmful. Our results suggest that the formulation of possible functional foods should approximate as much as possible the natural environment in which active molecules are found.
引用
收藏
页码:383 / 391
页数:9
相关论文
共 60 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]   Trans-10, cis-12-and cis-9, trans-11-conjugated linoleic acid isomers selectively modify HDL-apolipoprotein composition in apolipoprotein E knockout mice [J].
Arbonés-Mainar, JM ;
Navarro, MA ;
Acín, S ;
Guzmán, MA ;
Arnal, C ;
Surra, JC ;
Carnicer, R ;
Roche, HM ;
Osada, J .
JOURNAL OF NUTRITION, 2006, 136 (02) :353-359
[3]  
ARZOLAN N, 1995, J BIOL CHEM, V270, P19833
[4]   Atheroprotective effects of high-density lipoproteins [J].
Assmann, G ;
Nofer, JR .
ANNUAL REVIEW OF MEDICINE, 2003, 54 :321-341
[5]   Hydroxycinnamic acids do not prevent aortic atherosclerosis in hypercholesterolemic golden Syrian hamsters [J].
Auger, C ;
Laurent, N ;
Laurent, C ;
Besançon, P ;
Caporiccio, B ;
Teissédre, PL ;
Rouanet, JM .
LIFE SCIENCES, 2004, 74 (19) :2365-2377
[6]  
Bonanome A, 2000, NUTR METAB CARDIOVAS, V10, P111
[7]   High density lipoproteins (HDL) and the oxidative hypothesis of atherosclerosis [J].
Bonnefont-Rousselot, D ;
Thérond, P ;
Beaudeux, JL ;
Peynet, J ;
Legrand, A ;
Delattre, J .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 1999, 37 (10) :939-948
[8]  
Boskou D, 2000, World Rev Nutr Diet, V87, P56
[9]  
Brousseau ME, 1999, J LIPID RES, V40, P365
[10]   Effects of dietary fat amount and saturation on the regulation of hepatic mRNA and plasma apolipoprotein A-I in rats [J].
Calleja, L ;
Trallero, MC ;
Carrizosa, C ;
Méndez, MT ;
Palacios-Alaiz, E ;
Osada, J .
ATHEROSCLEROSIS, 2000, 152 (01) :69-78