Modulation of the regression of atherosclerosis in the hamster by dietary lipids: comparison of coconut oil and olive oil

被引:29
作者
Mangiapane, EH
McAteer, MA
Benson, GM
White, DA
Salter, AM
机构
[1] Univ Nottingham, Sch Biol Sci, Div Nutr Biochem, Loughborough LE12 5RD, Leics, England
[2] SmithKline Beecham Pharmaceut Ltd, Vasc Biol Dept, Harlow CM19 5AW, Essex, England
[3] Univ Nottingham, Sch Med, Sch Biomed Sci, Nottingham NG7 2UH, England
关键词
hamster; atherosclerosis; coconut oil; olive oil; dietary fat;
D O I
10.1017/S0007114599001646
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The Golden Syrian hamster (Mesocricetus auratus) has been shown to be a useful model of both human lipoprotein metabolism and the development of atherosclerosis. We report the effects of dietary lipids on the progression and regression of atherosclerosis in this model. In the first study, hamsters fed on coconut oil (150 g/kg diet) and cholesterol (30 g/kg diet) developed lip:td-rich lesions in the ascending aorta (0.28 (SD 0.14)mm(2)) and aortic arch (0.01 (SD 0.01) mm(2)) after 4 weeks that continued to progress over the next 8 weeks (0.75 (SD 0.41) mm(2) and 0.12 (SD 0.11) mm(2) for the ascending aorta and aortic arch respectively). Removal of cholesterol from the diet halted this progression. Furthermore, in animals fed on olive oil in the absence of added cholesterol, plasma LDL-cholesterol concentrations were lower (P < 0.05) and the extent of atherosclerotic lesions was reduced (P< 0.001 for both regions of the aorta) compared with animals fed on coconut oil (with no added cholesterol). In a second study, animals were fed on the atherogenic diet for 10 weeks, transferred to diets containing either coconut oil (150 g/kg diet) or olive oil (150 g/kg diet) without added cholesterol and monitored for up to 16 weeks. In the ascending aorta, lesion size doubled in animals fed on coconut oil but stabilized in those fed on olive oil. In the aortic arch, lesion size decreased linearly (P < 0.05, P < 0.001 for coconut oil and olive oil respectively) with the greatest reduction being seen in the olive-oil-fed animals (P < 0.05). Again, progression and regression of atherosclerosis appeared to reflect the relative concentrations of LDL-cholesterol and HDL-cholesterol in the plasma. We conclude that the male Golden Syrian hamster represents a useful model of dietary induced regression as well as progression of atherosclerosis.
引用
收藏
页码:401 / 409
页数:9
相关论文
共 31 条
[1]   MODULATION OF HEPATIC APOLIPOPROTEIN-B, 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE AND LOW-DENSITY-LIPOPROTEIN RECEPTOR MESSENGER-RNA AND PLASMA-LIPOPROTEIN CONCENTRATIONS BY DEFINED DIETARY FATS - COMPARISON OF TRIMYRISTIN, TRIPALMITIN, TRISTERIN AND TRIOLEIN [J].
BENNETT, AJ ;
BILLETT, MA ;
SALTER, AM ;
MANGIAPANE, EH ;
BRUCE, JS ;
ANDERTON, KL ;
MARENAH, CB ;
LAWSON, N ;
WHITE, DA .
BIOCHEMICAL JOURNAL, 1995, 311 :167-173
[2]   Mouse models of atherosclerosis [J].
Breslow, JL .
SCIENCE, 1996, 272 (5262) :685-688
[3]  
FOXALL TL, 1992, AM J PATHOL, V140, P1357
[4]   MASSIVE XANTHOMATOSIS AND ATHEROSCLEROSIS IN CHOLESTEROL-FED LOW-DENSITY-LIPOPROTEIN RECEPTOR-NEGATIVE MICE [J].
ISHIBASHI, S ;
GOLDSTEIN, JL ;
BROWN, MS ;
HERZ, J ;
BURNS, DK .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (05) :1885-1893
[5]   Cholesterol response and foam cell formation in hamsters fed two levels of saturated fat and various levels of cholesterol [J].
Kahlon, TS ;
Chow, FI ;
Irving, DW ;
Sayre, RN .
NUTRITION RESEARCH, 1996, 16 (08) :1353-1368
[6]   DOXAZOSIN AND CHOLESTYRAMINE SIMILARLY DECREASE FATTY STREAK FORMATION IN THE AORTIC-ARCH OF HYPERLIPIDEMIC HAMSTERS [J].
KOWALA, MC ;
NUNNARI, JJ ;
DURHAM, SK ;
NICOLOSI, RJ .
ATHEROSCLEROSIS, 1991, 91 (1-2) :35-49
[7]   PROSTACYCLIN AGONISTS REDUCE EARLY ATHEROSCLEROSIS IN HYPERLIPIDEMIC HAMSTERS - OCTIMIBATE AND BMY 42393 SUPPRESS MONOCYTE CHEMOTAXIS, MACROPHAGE CHOLESTERYL ESTER ACCUMULATION, SCAVENGER RECEPTOR ACTIVITY, AND TUMOR-NECROSIS-FACTOR PRODUCTION [J].
KOWALA, MC ;
MAZZUCCO, CE ;
HARTL, KS ;
SEILER, SM ;
WARR, GA ;
ABID, S ;
GROVE, RI .
ARTERIOSCLEROSIS AND THROMBOSIS, 1993, 13 (03) :435-444
[8]  
LINDSEY S, 1990, P SOC EXP BIOL MED, V195, P261, DOI 10.3181/00379727-195-43145
[9]  
MAHLER VMG, 1995, ATHEROSCLEROSIS, V118, pS91
[10]   APOE-DEFICIENT MICE DEVELOP LESIONS OF ALL PHASES OF ATHEROSCLEROSIS THROUGHOUT THE ARTERIAL TREE [J].
NAKASHIMA, Y ;
PLUMP, AS ;
RAINES, EW ;
BRESLOW, JL ;
ROSS, R .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (01) :133-140