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载脂蛋白 CIII 转基因兔血脂三酰甘油升高及脂肪清除延迟

Hypertriglyceridemia and delayed clearance of fat load in transgenic rabbits expressing human apolipoprotein CIII.

机构信息

Institute of Cardiovascular Sciences and Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education, Peking University Health Science Center, 38 Xueyuan Road, Beijing, 100191, China.

出版信息

Transgenic Res. 2011 Aug;20(4):867-75. doi: 10.1007/s11248-010-9467-5. Epub 2010 Dec 1.

Abstract

Apolipoprotein CIII (apoCIII) has been implicated in hypertriglyceridemia and plasma apoCIII independently predicts risk for coronary heart disease. While hypertriglyceridemia in patients has been demonstrated to correlate with elevated plasma apoCIII levels and reduced lipoprotein lipase (LPL) activity, apoCIII transgenic mice show elevated LPL activity. In this study, we generated transgenic (Tg) rabbits expressing human apoCIII gene exclusively in liver and investigated the effect of apoCIII overexpression on lipid metabolism of rabbits. In comparison with non-Tg littermates, Tg rabbits had 3- and 3.2-fold increases in fed and fasted plasma triglycerides, respectively. In contrast, no significant differences were observed in plasma total cholesterol and high density lipoprotein cholesterol levels between Tg and non-Tg rabbits. Analysis of lipoprotein fractions revealed that elevated plasma triglyceride levels in Tg rabbits were mainly attributed to an increase in very low density lipoprotein/chylomicron-sized particles. Furthermore, Tg rabbits showed markedly delayed clearance of plasma triglycerides accompanied with significantly reduced LPL activity in post-heparin plasma compared to that in non-Tg controls. In conclusion, these results indicate apoCIII transgenic rabbits develop hypertriglyceridemia with similar mechanism in hypertriglyceridemic patients via delayed clearance of plasma triglycerides, and could be used as a valuable tool for the study of human hyperlipidemia in relation with atherosclerotic disorders.

摘要

载脂蛋白 CIII(apoCIII)与高甘油三酯血症有关,且血浆 apoCIII 水平独立预测冠心病风险。虽然患者的高甘油三酯血症与血浆 apoCIII 水平升高和脂蛋白脂肪酶(LPL)活性降低相关,但 apoCIII 转基因小鼠显示 LPL 活性升高。在这项研究中,我们生成了专门在肝脏中表达人 apoCIII 基因的转基因(Tg)兔,并研究了 apoCIII 过表达对兔脂质代谢的影响。与非 Tg 同窝仔兔相比,Tg 兔的进食和禁食后血浆甘油三酯分别增加了 3 倍和 3.2 倍。相比之下,Tg 和非 Tg 兔的血浆总胆固醇和高密度脂蛋白胆固醇水平没有显著差异。脂蛋白组分分析表明,Tg 兔血浆甘油三酯水平升高主要归因于极低密度脂蛋白/乳糜微粒大小颗粒的增加。此外,与非 Tg 对照组相比,Tg 兔的血浆甘油三酯清除明显延迟,肝素后血浆中的 LPL 活性显著降低。总之,这些结果表明,apoCIII 转基因兔通过延迟清除血浆甘油三酯而类似于高甘油三酯血症患者发生高甘油三酯血症,并且可作为研究与动脉粥样硬化疾病相关的人类高脂血症的有价值工具。

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