使用区室分析描述饮食脂肪饱和度和负荷对大鼠血浆甘油三酯动力学的影响。

Progress in food & nutrition science Pub Date : 1988-01-01
M H Green, P L Faulkner, J B Green
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引用次数: 0

摘要

采用基于模型的室室分析来解释大鼠慢性输注乳糜微粒(CM)后血浆甘油三酯(TG)反应的时间变化数据。雄性大鼠饲喂不同脂肪负荷(L = 10% (w/w), H = 30%)和P/S比(P = 4.6, S = 0.2)的纯化饲料。从吸收P或S脂肪的供体大鼠分离的淋巴CM连续3天输注给受体8 h,在第1天和第3天,CM输注率反映前一种饮食的脂肪含量,在第2天,另一种负荷;这种输注代替了饮食中的脂肪。对每个时期的连续血浆样本进行TG浓度分析;3 d后测定TG在血浆脂蛋白和肝脏脂质的分布。为了描述观测到的群体平均数据,利用计算机模拟、分析和建模程序建立了一个隔间模型。血浆中需要两个区室(CM vs非CM TG);每个都有2个输出:脂蛋白脂肪酶(LPL)去除tg脂肪酸和肝脏摄取残余脂蛋白。在肝脏延迟后,tg衍生的脂肪酸有三种结局:氧化、滞留或以极低密度脂蛋白的形式分泌。模拟CM总TG转换速率常数的变化表明,LPL基础水平在TG输注后迅速显著升高;3 ~ 5 H后,LPL表观活性下降。对CM TG周转率的模拟表明,在注射开始后,周转率立即上升到高于注射速度的水平,然后进入轻微的负平衡。虽然观察到的数据可以根据目前对TG代谢的理解进行定性描述,但基于模型的区室分析的应用产生了关于系统动力学定量方面的可测试假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of compartmental analysis to describe effects of dietary fat saturation and load on plasma triglyceride dynamics in the rat.

Model-based compartmental analysis was used to interpret data on temporal changes in plasma triglyceride (TG) response to a chronic infusion of chylomicrons (CM) in the rat. Male rats were fed purified diets which varied in fat load [L = 10% (w/w), H = 30%] and P/S ratio (P = 4.6, S = 0.2). Lymph CM isolated from donor rats which were absorbing the P or S fat were infused into recipients for 8 h on 3 consecutive days: on d 1 and 3, CM infusion rate reflected the fat content of the previous diet and on d 2, the other load; the infusion replaced dietary fat. Serial plasma samples from each period were analyzed for TG concentration; TG distribution in plasma lipoproteins and liver lipids was measured after d 3. To describe observed group average data, a compartmental model was developed using the Simulation, Analysis and Modeling computer program. Two compartments were needed in plasma (CM vs nonCM TG); each had 2 outputs: removal of TG-fatty acids by lipoprotein lipase (LPL) and uptake of remnant lipoproteins by the liver. After a delay in the liver, there were 3 fates for TG-derived fatty acids: oxidation, retention, or secretion in very low density lipoproteins. Simulation of changes in the rate constant for total CM TG turnover indicated that the basal level of LPL rose rapidly and dramatically in response to TG infusion; the rise was higher for H vs L. After 3-5 h, apparent LPL activity decreased. Simulation of the rate of CM TG turnover indicated that the turnover rate rose immediately after infusion began to levels higher than the infusion rate, and then came into a slight negative balance. Although the observed data could be qualitatively described based on current understanding of TG metabolism, application of model-based compartmental analysis generated testable hypotheses about quantitative aspects of the system dynamics.

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