Suppr超能文献

正常血脂犬静脉注射曲通WR - 1339后的血浆脂蛋白变化:对高密度脂蛋白的优先作用

Plasma lipoprotein changes attending the intravenous administration of Triton WR-1339 in normolipidemic dogs: preferential effect on high density lipoproteins.

作者信息

Edelstein C, Byrne R E, Yamamoto K, Zarins C, Scanu A M

出版信息

J Lipid Res. 1985 Mar;26(3):351-9.

PMID:3921637
Abstract

The nonionic detergent Triton WR-1339 was injected intravenously into normolipidemic dogs in a single dose of 150 mg/kg body weight followed by three other injections (75 mg/kg) on days 2, 6, and 12. The Triton produced a significant elevation of the plasma cholesterol of these animals, but not of their triglyceride levels, and profound changes of their plasma lipoproteins, particularly of the high density lipoprotein class. These changes were dependent on the concentration of Triton attained in plasma; when the levels were above 1.5 mg/ml, density gradient ultracentrifugation, electrophoretic, and chemical analyses indicated that an interaction between Triton and HDL had occurred. This interaction was attended by a gradual loss of the surface components of HDL, namely apoA-I, phospholipids, and unesterified cholesterol, and by the appearance of two cholesteryl ester-rich lipoproteins of d 1.019-1.024 g/ml and d 1.038-1.058 g/ml containing apoA-I and proteins with electrophoretic mobilities of apoB, apoE, and apoA-IV. At the time that these changes had occurred, the activities of the enzymes lecithin: cholesterol acyltransferase and post-heparin lipase were unaffected. When 125I-labeled apoA-I was injected intravenously into animals receiving Triton, the residence time of the radiolabeled protein in plasma increased from a control value of 3.1 days to 7.2 days. However, the apparent half-times of the radiolabeled apoA-I varied among the lipoprotein fractions it was associated with: d 1.119-1.159 g/ml, 5.28 days; d 1.019-1.024 g/ml, 7.55 days, and d 1.038-1.058 g/ml, 5.39 days.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

将非离子去污剂曲拉通WR - 1339以150毫克/千克体重的单次剂量静脉注射到血脂正常的犬体内,随后在第2、6和12天进行另外三次注射(75毫克/千克)。曲拉通使这些动物的血浆胆固醇显著升高,但甘油三酯水平未升高,并且其血浆脂蛋白发生了深刻变化,尤其是高密度脂蛋白类别。这些变化取决于血浆中达到的曲拉通浓度;当水平高于1.5毫克/毫升时,密度梯度超速离心、电泳和化学分析表明曲拉通与高密度脂蛋白之间发生了相互作用。这种相互作用伴随着高密度脂蛋白表面成分即载脂蛋白A - I、磷脂和未酯化胆固醇的逐渐丧失,以及出现两种富含胆固醇酯的脂蛋白,其密度分别为1. = 019 - 1.024克/毫升和1.038 - 1.058克/毫升,含有载脂蛋白A - I以及电泳迁移率与载脂蛋白B、载脂蛋白E和载脂蛋白A - IV相同的蛋白质。在这些变化发生时,卵磷脂胆固醇酰基转移酶和肝素后脂肪酶的活性未受影响。当将125I标记的载脂蛋白A - I静脉注射到接受曲拉通治疗的动物体内时,放射性标记蛋白在血浆中的停留时间从对照值3.1天增加到7.2天。然而,放射性标记的载脂蛋白A - I在与其相关的脂蛋白组分中的表观半衰期各不相同:密度为1.119 - 1.159克/毫升的组分,半衰期为5.28天;密度为1.019 - 1.024克/毫升的组分,半衰期为7.55天;密度为1.038 - 1.058克/毫升的组分,半衰期为5.39天。(摘要截断于250字)

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