Suppr超能文献

稳态甘油三酯吸收过程中大鼠肠淋巴中的载脂蛋白组成与周转

Apoprotein composition and turnover in rat intestinal lymph during steady-state triglyceride absorption.

作者信息

Holt P R, Wu A L, Clark S B

出版信息

J Lipid Res. 1979 May;20(4):494-502.

PMID:222857
Abstract

Apoproteins of chylomicrons, very low density lipoprotein (VLDL), and a low density + high density fraction secreted by proximal and distal rat small intestine into mesenteric lymph were examined during triglyceride (TG) absorption. Apoprotein output and composition were determined and the turnover rates of labeled non-apoB (soluble) apoproteins in lipoprotein fractions were measured after an intraluminal [(3)H]leucine pulse during stable TG transport into lymph. The output of VLDL apoproteins exceeded that of chylomicrons during the absorption of 45 micro mol of TG per hour. More [(3)H]leucine was incorporated into VLDL than into chylomicrons and the decay of newly synthesized VLDL apoproteins was more rapid than that of chylomicrons, in part due to higher concentrations of apoA-I and apoA-IV with a rapid turnover rate. Chylomicrons from proximal intestine contained more apoA-I and less C peptides than chylomicrons from distal intestine. Ninety percent of [(3)H]leucine incorporated into soluble apoproteins was in apoA-I and apoA-IV, but little apoARP was labeled. The turnover rate of apoA-I and apoA-IV differed significantly in the lymph lipoproteins examined. Although total C peptide labeling was small, evidence for intestinal apoC-II formation and differing patterns of apoC-III subunit labeling was obtained. [(3)H]Leucine incorporation and apoprotein turnover rates in lipoprotein secreted by proximal and distal intestine were similar. The different turnover rates of apoA-I and apoA-IV in individual lipoproteins suggest that these A apoproteins are synthesized independently in the intestine.-Holt, P. R., A-L. Wu, and S. Bennett Clark. Apoprotein composition and turnover in rat intestinal lymph during steady-state triglyceride absorption.

摘要

在甘油三酯(TG)吸收过程中,对大鼠近端和远端小肠分泌到肠系膜淋巴中的乳糜微粒、极低密度脂蛋白(VLDL)以及低密度+高密度脂蛋白组分的载脂蛋白进行了检测。测定了载脂蛋白的输出量和组成,并在稳定的TG转运至淋巴过程中,经肠腔内[³H]亮氨酸脉冲后,测量了脂蛋白组分中标记的非载脂蛋白B(可溶性)载脂蛋白的周转率。在每小时吸收45微摩尔TG的过程中,VLDL载脂蛋白的输出量超过了乳糜微粒。与乳糜微粒相比,更多的[³H]亮氨酸掺入到VLDL中,新合成的VLDL载脂蛋白的衰减比乳糜微粒更快,部分原因是apoA-I和apoA-IV浓度较高且周转率较快。近端小肠的乳糜微粒比远端小肠的乳糜微粒含有更多的apoA-I和更少的C肽。掺入可溶性载脂蛋白的[³H]亮氨酸中有90%存在于apoA-I和apoA-IV中,但几乎没有apoARP被标记。在所检测的淋巴脂蛋白中,apoA-I和apoA-IV的周转率有显著差异。尽管总的C肽标记量很少,但获得了肠道apoC-II形成的证据以及apoC-III亚基标记的不同模式。近端和远端小肠分泌的脂蛋白中[³H]亮氨酸掺入量和载脂蛋白周转率相似。单个脂蛋白中apoA-I和apoA-IV的不同周转率表明,这些A类载脂蛋白在肠道中是独立合成的。-霍尔特,P.R.,A-L.吴,和S.贝内特·克拉克。稳态甘油三酯吸收过程中大鼠肠道淋巴中的载脂蛋白组成和周转率。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验