Jones Peter J H, Demonty Isabelle, Chan Yen-Ming, Herzog Yael, Pelled Dori
School of Dietetics and Human Nutrition, McGill University, Sainte-Anne-de-Bellevue, Canada.
Lipids Health Dis. 2007 Oct 25;6:28. doi: 10.1186/1476-511X-6-28.
Consumption of plant sterol (PS) esters lower low-density lipoprotein (LDL)-cholesterol levels by suppressing intestinal absorption of cholesterol. Commercially available PS are mainly esterified to omega-6 fatty acid (FA), such as sunflower oil (SO) FA. Emerging trends include using other sources such as olive oil (OO) or omega-3 FA from fish oil (FO), known to exert potent hypotriglyceridemic effects. Our objective was to compare the actions of different FA esterified to PS on blood lipids, carotenoid bioavailability as well as inflammatory and coagulation markers.
Twenty-one moderately overweight, hypercholesterolemic subjects consumed experimental isoenergetic diets enriched with OO (70% of fat), each lasting 28-day and separated by 4-week washout periods, using a randomized crossover design. Diets were supplemented with three PS esters preparations, PS-FO, PS-SO, or PS-OO. All PS treatments contained an equivalent of 1.7 PS g/d, and the PS-FO provided a total of 5.4 g/d FO FA (eicosapentaenoic and docosahexaenoic acids).
There were no differences between PS-containing diet effects on total cholesterol, LDL-cholesterol, or high-density lipoprotein (HDL)-cholesterol levels. However, PS-FO consumption resulted in markedly lower (P < 0.0001) fasting and postprandial triglyceride concentrations compared with PS-SO and PS-OO. These treatments affected plasma beta-carotene (P = 0.0169) and retinol (P = 0.0244), but not tocopherol (P = 0.2108) concentrations. Consumption of PS-FO resulted in higher beta-carotene (P = 0.0139) and retinol (P = 0.0425) levels than PS-SO and PS-OO, respectively. Plasma TNF-alpha, IL-6, C-reactive protein, prostate specific antigen, and fibrinogen concentrations were unaffected by the PS-interventions. In contrast, plasminogen activator inhibitor 1 (PAI-1) concentrations were lower (P = 0.0282) in the PS-FO-fed than the PS-SO, but not the PS-OO (P = 0.7487) groups.
Our findings suggest that, in hypercholesterolemic subjects consuming an OO-based diet, PS-FO results in lowered blood triglyceride and PAI-1 concentrations, and higher fat-soluble vitamin levels in comparison to the vegetable oil FA esters of PS (PS-SO and PS-OO). Thus, PS-FO may offer hyperlipidemic subjects a more comprehensive lipid lowering approach while reducing the potential risk of decreased plasma carotenoid concentrations.
食用植物甾醇(PS)酯可通过抑制肠道对胆固醇的吸收来降低低密度脂蛋白(LDL)胆固醇水平。市售的PS主要与ω-6脂肪酸(FA)酯化,如向日葵油(SO)FA。新趋势包括使用其他来源,如橄榄油(OO)或鱼油(FO)中的ω-3 FA,已知这些物质具有强大的降甘油三酯作用。我们的目的是比较与PS酯化的不同FA对血脂、类胡萝卜素生物利用度以及炎症和凝血标志物的作用。
21名中度超重的高胆固醇血症受试者采用随机交叉设计,食用富含OO(占脂肪的70%)的等能量实验饮食,每种饮食持续28天,中间间隔4周的洗脱期。饮食中补充三种PS酯制剂,即PS-FO、PS-SO或PS-OO。所有PS处理均含有相当于1.7 g/d的PS,且PS-FO总共提供5.4 g/d的FO FA(二十碳五烯酸和二十二碳六烯酸)。
含PS饮食对总胆固醇、LDL胆固醇或高密度脂蛋白(HDL)胆固醇水平的影响无差异。然而,与PS-SO和PS-OO相比,食用PS-FO导致空腹和餐后甘油三酯浓度显著降低(P < 0.0001)。这些处理影响血浆β-胡萝卜素(P = 0.0169)和视黄醇(P = 0.0244)浓度,但不影响生育酚(P = 0.2108)浓度。与PS-SO和PS-OO相比,食用PS-FO分别导致更高的β-胡萝卜素(P = 0.0139)和视黄醇(P = 0.0425)水平。血浆肿瘤坏死因子-α、白细胞介素-6、C反应蛋白、前列腺特异性抗原和纤维蛋白原浓度不受PS干预的影响。相反,PS-FO喂养组的纤溶酶原激活物抑制剂1(PAI-1)浓度低于PS-SO组(P = 0.0282),但与PS-OO组相比无差异(P = 0.7487)。
我们的研究结果表明,在食用以OO为基础饮食的高胆固醇血症受试者中,与PS的植物油FA酯(PS-SO和PS-OO)相比,PS-FO可降低血液甘油三酯和PAI-1浓度,并提高脂溶性维生素水平。因此,PS-FO可能为高脂血症患者提供一种更全面的降脂方法,同时降低血浆类胡萝卜素浓度降低的潜在风险。