Parks E J, Krauss R M, Christiansen M P, Neese R A, Hellerstein M K
Department of Food Science and Nutrition, University of Minnesota-Twin Cities, St. Paul, Minnesota 55108, USA.
J Clin Invest. 1999 Oct;104(8):1087-96. doi: 10.1172/JCI6572.
Low-fat, high-carbohydrate (LF/HC) diets commonly elevate plasma triglyceride (TG) concentrations, but the kinetic mechanisms responsible for this effect remain uncertain. Subjects with low TG (normolipidemic [NL]) and those with moderately elevated TG (hypertriglyceridemic [HTG]) were studied on both a control and an LF/HC diet. We measured VLDL particle and TG transport rates, plasma nonesterified fatty acid (NEFA) flux, and sources of fatty acids used for the assembly of VLDL-TG. The LF/HC diet resulted in a 60% elevation in TG, a 37% reduction in VLDL-TG clearance, and an 18% reduction in whole-body fat oxidation, but no significant change in VLDL-apo B or VLDL-TG secretion rates. Significant elevations in fasting apo B-48 concentrations were observed on the LF/HC in HTG subjects. In both groups, fasting de novo lipogenesis was low regardless of diet. The NEFA pool contributed the great majority of fatty acids to VLDL-TG in NL subjects on both diets, whereas in HTG subjects, the contribution of NEFA was somewhat lower overall and was reduced further in individuals on the LF/HC diet. Between 13% and 29% of VLDL-TG fatty acids remained unaccounted for by the sum of de novo lipogenesis and plasma NEFA input in HTG subjects. We conclude that (a) whole-food LF/HC diets reduce VLDL-TG clearance and do not increase VLDL-TG secretion or de novo lipogenesis; (b) sources of fatty acids for assembly of VLDL-TG differ between HTG and NL subjects and are further affected by diet composition; (c) the presence of chylomicron remnants in the fasting state on LF/HC diets may contribute to elevated TG levels by competing for VLDL-TG lipolysis and by providing a source of fatty acids for hepatic VLDL-TG synthesis; and (d) the assembly, production, and clearance of elevated plasma VLDL-TG in response to LF/HC diets therefore differ from those for elevated TG on higher-fat diets.
低脂高碳水化合物(LF/HC)饮食通常会使血浆甘油三酯(TG)浓度升高,但导致这种效应的动力学机制仍不明确。对甘油三酯水平较低(血脂正常[NL])和甘油三酯中度升高(高甘油三酯血症[HTG])的受试者分别采用对照饮食和LF/HC饮食进行研究。我们测量了极低密度脂蛋白(VLDL)颗粒和TG转运速率、血浆非酯化脂肪酸(NEFA)通量以及用于组装VLDL-TG的脂肪酸来源。LF/HC饮食导致TG升高60%,VLDL-TG清除率降低37%,全身脂肪氧化减少18%,但VLDL-载脂蛋白B(apo B)或VLDL-TG分泌率无显著变化。在HTG受试者中,LF/HC饮食使空腹apo B-48浓度显著升高。在两组中,无论饮食如何,空腹时的从头脂肪生成均较低。在两种饮食状态下,NL受试者中,NEFA库为VLDL-TG提供了绝大多数脂肪酸,而在HTG受试者中,NEFA的总体贡献略低,并且在LF/HC饮食的个体中进一步降低。在HTG受试者中,从头脂肪生成和血浆NEFA输入之和仍无法解释13%至29%的VLDL-TG脂肪酸来源。我们得出以下结论:(a)全食物LF/HC饮食会降低VLDL-TG清除率,且不会增加VLDL-TG分泌或从头脂肪生成;(b)HTG和NL受试者中用于组装VLDL-TG的脂肪酸来源不同,且受饮食组成的进一步影响;(c)LF/HC饮食状态下空腹时乳糜微粒残粒的存在可能通过竞争VLDL-TG脂解作用并为肝脏VLDL-TG合成提供脂肪酸来源,从而导致TG水平升高;(d)因此,响应LF/HC饮食时血浆VLDL-TG升高的组装、产生和清除过程与高脂肪饮食导致TG升高的情况不同。