Zech L A, Grundy S M, Steinberg D, Berman M
J Clin Invest. 1979 Jun;63(6):1262-73. doi: 10.1172/JCI109421.
A model for the synthesis and degradation of very low density lipoprotein triglyceride (VLDL-TG) in man is proposed to explain plasma VLDL-TG radioactivity data from studies conducted over a 48-h interval after injection of glycerol labeled with 14C, 3H, or both. The curve describing the radioactivity of plasma VLDL triglycerides reaches a maximum at about 2 h, after which the decay is biphasic in all cases; the late curvature becoming evident only after 8--12 h. To fit the complex curve, it was necessary to postulate two pathways for the incorporation of plasma glycerol into VLDL-TG, one much slower than the other. A process of stepwise delipidation of VLDL in the plasma compartment, previously proposed for VLDL apoprotein models, was also necessary. Predicted VLDL-TG synthesis rates calculated with this model can differ significantly from those based on experiments of shorter duration in which the slow VLDL-TG component is not apparent. The results of these studies strongly support the interpretation that the late, slow component of the VLDL-TG activity curve is predominantly due to the slowly turning-over precursor compartment in the conversion pathway and is not due either to a slow compartment in the labeled precursor, plasma free glycerol, or to an exchange of plasma VLDL-TG with an extravascular compartment. It also cannot, in these studies, be attributed to a slowly turning-over VLDL-TG moiety in the plasma. The model was tested with data from 59 studies including normal subjects and patients with obesity and(or) various forms of hyperlipoproteinemia. Good fits were obtained in all cases, and the estimated parameter values and their uncertainties for 13 normolipemic nonobese subjects are presented. Sensitivty testing was carried out to determine how critical various parameter estimations are to the assumptions introduced in the modeling.
本文提出了一个人体极低密度脂蛋白甘油三酯(VLDL-TG)合成与降解的模型,以解释在注射用14C、3H或两者标记的甘油后48小时内所进行研究的血浆VLDL-TG放射性数据。描述血浆VLDL甘油三酯放射性的曲线在约2小时达到最大值,此后在所有情况下衰减均呈双相;后期曲率仅在8 - 12小时后才变得明显。为了拟合这条复杂的曲线,有必要假定血浆甘油掺入VLDL-TG存在两条途径,其中一条比另一条慢得多。此前针对VLDL载脂蛋白模型提出的血浆中VLDL逐步脱脂过程也是必要的。用该模型计算出的预测VLDL-TG合成速率可能与基于较短时长实验得出的速率有显著差异,在较短时长实验中,缓慢的VLDL-TG成分并不明显。这些研究结果有力地支持了这样一种解释,即VLDL-TG活性曲线后期的缓慢成分主要归因于转化途径中周转缓慢的前体区室,而非归因于标记前体(血浆游离甘油)中的缓慢区室,也不是由于血浆VLDL-TG与血管外区室之间的交换。在这些研究中,它也不能归因于血浆中周转缓慢的VLDL-TG部分。该模型用来自59项研究的数据进行了测试,包括正常受试者以及肥胖和(或)各种形式高脂血症患者。在所有情况下都获得了良好的拟合,并给出了13名血脂正常的非肥胖受试者的估计参数值及其不确定性。进行了敏感性测试,以确定各种参数估计对建模中引入的假设的关键程度。