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静脉注射普朗尼克L-81对用曲拉通WR-1339处理的禁食大鼠的降血脂作用:对肝脂蛋白分泌的可能抑制作用

Hypolipidemic effect of intravenous pluronic L-81 in fasted rats treated with Triton WR-1339: possible inhibition of hepatic lipoprotein secretion.

作者信息

Nutting D F, Tso P

机构信息

Department of Physiology and Biophysics, University of Tennessee, Memphis.

出版信息

Horm Metab Res. 1989 Mar;21(3):113-5. doi: 10.1055/s-2007-1009167.

DOI:10.1055/s-2007-1009167
PMID:2744715
Abstract

Pluronic L-81 (L-81), a non-ionic hydrophobic surfactant, is a powerful inhibitor of the secretion of lipid-transporting chylomicrons from intestinal epithelial cells to lymph. Since the other major organ that secretes lipoproteins into the circulation is the liver, whose principal lipid secretory product is very low density lipoprotein (VLDL), we tested the hypothesis that L-81 will also inhibit hepatic lipid secretion. Rats were fasted so that they had little lipid input from the intestine. We then administered Triton WR-1339 (tyloxapol) intravenously to block peripheral utilization of VLDL, causing plasma lipids to rise rapidly. Some animals were also given L-81 intravenously to test whether the L-81 would retard the tyloxapol-induced rise in plasma lipids. Administration of tyloxapol alone (250 mg/kg) increased plasma triglyceride, phospholipid and cholesterol concentrations considerably. Simultaneous administration of a small dose of L-81 (6 mg/kg) markedly reduced the rise in plasma triglyceride, particularly in the first hour (by 45%). L-81 also diminished the rise in plasma phospholipid and cholesterol, but to a lesser extent (30%). In the fasting rat, most of the plasma triglyceride is in VLDL; therefore, L-81 probably acts by decreasing the secretion of hepatic VLDL. Thus, Pluronic L-81 may be a useful tool for examining the secretion and metabolism of hepatic lipoproteins, in particular, VLDL.

摘要

普朗尼克L-81(L-81)是一种非离子型疏水表面活性剂,是肠道上皮细胞向淋巴分泌脂质转运乳糜微粒的强力抑制剂。由于另一个向循环系统分泌脂蛋白的主要器官是肝脏,其主要脂质分泌产物是极低密度脂蛋白(VLDL),我们检验了L-81也会抑制肝脏脂质分泌的假说。将大鼠禁食,使其肠道几乎没有脂质输入。然后静脉注射曲拉通WR-1339(聚乙氧基月桂醇)以阻断VLDL的外周利用,导致血浆脂质迅速升高。一些动物还静脉注射L-81,以测试L-81是否会延缓曲拉通诱导的血浆脂质升高。单独给予曲拉通(250mg/kg)可使血浆甘油三酯、磷脂和胆固醇浓度显著升高。同时给予小剂量的L-81(6mg/kg)可显著降低血浆甘油三酯的升高,尤其是在第一个小时(降低45%)。L-81也减少了血浆磷脂和胆固醇的升高,但程度较小(30%)。在禁食大鼠中,大部分血浆甘油三酯存在于VLDL中;因此,L-81可能通过减少肝脏VLDL的分泌起作用。因此,普朗尼克L-81可能是研究肝脏脂蛋白,特别是VLDL的分泌和代谢的有用工具。

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1
Hypolipidemic effect of intravenous pluronic L-81 in fasted rats treated with Triton WR-1339: possible inhibition of hepatic lipoprotein secretion.静脉注射普朗尼克L-81对用曲拉通WR-1339处理的禁食大鼠的降血脂作用:对肝脂蛋白分泌的可能抑制作用
Horm Metab Res. 1989 Mar;21(3):113-5. doi: 10.1055/s-2007-1009167.
2
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J Lipid Res. 1986 Feb;27(2):196-207.
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Plasma lipoproteins in streptozotocin-diabetic rats, after Triton WR-1339 treatment.经曲拉通WR - 1339处理的链脲佐菌素诱导的糖尿病大鼠的血浆脂蛋白
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Hypolipidemic activity of Achyranthus aspera Linn in normal and triton induced hyperlipemic rats.牛膝在正常及 Triton 诱导的高脂血症大鼠中的降血脂活性。
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[The lipid metabolism of the small intestine and its correlation to the lipid and lipoprotein metabolism of the total organism].[小肠的脂质代谢及其与整个机体脂质和脂蛋白代谢的相关性]
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Protective effect of rutin on lipids, lipoproteins, lipid metabolizing enzymes and glycoproteins in streptozotocin-induced diabetic rats.芦丁对链脲佐菌素诱导的糖尿病大鼠脂质、脂蛋白、脂质代谢酶和糖蛋白的保护作用。
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Effect of pluronic L-81 on intestinal lipoprotein secretion in the rat.普朗尼克L-81对大鼠肠道脂蛋白分泌的影响。
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Pharmacological study of nine antimicrotubular drugs with acrylophenone structure on Triton WR 1339-induced hyperlipidemia in rats.九种具有苯乙酮结构的抗微管药物对 Triton WR 1339 诱导的大鼠高脂血症的药理学研究。
Methods Find Exp Clin Pharmacol. 1985 Nov;7(11):579-83.

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