Nutting D F, Tso P
Department of Physiology and Biophysics, University of Tennessee, Memphis.
Horm Metab Res. 1989 Mar;21(3):113-5. doi: 10.1055/s-2007-1009167.
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.
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。