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首页> 外文期刊>Nutrition Research >A high-fat diet and the threonine-encoding allele (Thr54) polymorphism of fatty acid-binding protein 2 reduce plasma triglyceride-rich lipoproteins.
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A high-fat diet and the threonine-encoding allele (Thr54) polymorphism of fatty acid-binding protein 2 reduce plasma triglyceride-rich lipoproteins.

机译:高脂饮食和脂肪酸结合蛋白2的苏氨酸编码等位基因(Thr54)多态性会降低血浆富含甘油三酸酯的脂蛋白。

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摘要

The threonine-encoding allele (Thr54) of the fatty acid-binding protein 2 (FABP2) DNA polymorphism is associated with increased triglyceride (TG)-rich lipoproteins (TRL). We hypothesized that the TRL response to diets of varied fat content is affected by the FABP2 A54T polymorphism, specifically that a high-fat diet would reduce TRL and that the Thr54 allele would have an enhanced response. Sixteen healthy, postmenopausal women completed a crossover dietary intervention that included three 8-week, isoenergetic diet treatments. The treatments consisted of high fat (40% of energy as fat), low fat (20% of energy), and low fat + n-3 fatty acids (20% of energy plus 3% as n-3 fatty acids). Eight subjects were homozygous for the wild type (Ala54/Ala54) of the FABP2 polymorphism, whereas 8 subjects had at least 1 Thr54 allele (7, Ala54/Thr54; 1, Thr54/Thr54). High-fat diet showed significantly reduced plasma TGs, chylomicron TG, and very low-density lipoprotein TG from baseline in all participants. Although carriers of the Thr54 allele of the FABP2 polymorphism had significantly reduced TRL, there is no evidence of an interaction, which does not support our hypothesis. The alanine-encoding allele did not influence the dietary effects on the plasma lipids
机译:脂肪酸结合蛋白2(FABP2)DNA多态性的苏氨酸编码等位基因(Thr54)与富含甘油三酸酯(TG)的脂蛋白(TRL)增加有关。我们假设FABP2 A54T多态性会影响对脂肪含量不同的饮食的TRL反应,特别是高脂饮食会降低TRL,而Thr54等位基因的反应会增强。 16名健康,绝经后的妇女完成了一项交叉饮食干预,其中包括三项8周的等能量饮食治疗。治疗方法包括高脂肪(40%的能量为脂肪),低脂肪(20%的能量)和低脂肪+ n-3脂肪酸(20%的能量加3%的n-3脂肪酸)。八个受试者对于FABP2多态性的野生型(Ala54 / Ala54)是纯合的,而8个受试者具有至少1个Thr54等位基因(7,Ala54 / Thr54; 1,Thr54 / Thr54)。高脂饮食显示所有参与者的血浆TG,乳糜微粒TG和极低密度脂蛋白TG均较基线显着降低。尽管FABP2多态性的Thr54等位基因携带者的TRL显着降低,但没有相互作用的证据,这不支持我们的假设。编码丙氨酸的等位基因不影响饮食对血脂的影响

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