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饮食诱导磷脂转移蛋白缺陷小鼠的脂质蓄积:其动脉粥样硬化性及潜在机制。

Diet-induced lipid accumulation in phospholipid transfer protein-deficient mice: its atherogenicity and potential mechanism.

机构信息

Department of Cell Biology, State University of New York (SUNY) Downstate Medical Center, Brooklyn, NY, USA.

出版信息

J Lipid Res. 2010 Oct;51(10):2993-3002. doi: 10.1194/jlr.M007088. Epub 2010 Jun 11.

Abstract

A high saturated fat diet induces free cholesterol and phospholipid accumulation in the plasma of phospholipid transfer protein (Pltp)-deficient mice. In this study, we examined the atherogenic consequence of this phenomenon and investigated the possible mechanism(s). Pltp KO/Apoe KO mice that were fed a coconut oil-enriched high-fat diet (COD) for 7 weeks had higher plasma free cholesterol (149%), phospholipids (15%), and sphingomyelin (54%) than Apoe KO controls. In contrast to chow-fed animals, COD-fed Pltp KO/Apoe KO mice had the same atherosclerotic lesion size as that of Apoe KO mice. Similar to Pltp KO mice, plasma from COD-fed Pltp KO/Apoe KO mice contained VLDL/LDL-sized lamellar particles. Bile measurement indicated that COD-fed Pltp KO mice have 33% less hepatic cholesterol output than controls. In conclusion, COD-fed, Pltp-deficient mice are no longer protected from atherosclerosis and have impaired biliary lipid secretion, which is associated with free cholesterol and phospholipid accumulation.

摘要

高脂肪饮食可导致载脂蛋白 E 基因敲除(Apoe KO)小鼠的血浆磷脂转运蛋白(Pltp)缺乏,游离胆固醇和磷脂蓄积。本研究旨在观察该现象的致动脉粥样硬化作用,并探讨其可能的机制。7 周内给予富含椰子油的高脂肪饮食(COD)的 Pltp KO/Apoe KO 小鼠的血浆游离胆固醇(149%)、磷脂(15%)和神经鞘磷脂(54%)水平高于 Apoe KO 对照组。与正常饮食组动物不同,COD 饮食组 Pltp KO/Apoe KO 小鼠的动脉粥样硬化病变大小与 Apoe KO 小鼠相同。与 Pltp KO 小鼠相似,来自 COD 饮食组 Pltp KO/Apoe KO 小鼠的血浆中含有 VLDL/LDL 大小的层状颗粒。胆汁测量表明,与对照组相比,COD 饮食组 Pltp KO 小鼠的肝脏胆固醇输出减少了 33%。综上所述,缺乏 Pltp 的 COD 饮食小鼠不再免受动脉粥样硬化的影响,并且胆汁脂质分泌受损,这与游离胆固醇和磷脂蓄积有关。

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