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大鼠肠系膜淋巴中A-I及富含精氨酸载脂蛋白的起源与转运

Origin and transport of the A-I and arginine-rich apolipoproteins in mesenteric lymph of rats.

作者信息

Imaizumi K, Havel R J, Fainaru M, Vigne J L

出版信息

J Lipid Res. 1978 Nov;19(8):1038-46.

PMID:215684
Abstract

Transport of apolipoprotein A-I and argininerich apolipoprotein in mesenteric lymph was examined in rats given constant intraduodenal infusions of saline, glucose in saline, or emulsified fat. Lymph flow in all groups was constant from 5 to 50 hr after beginning the infusions. Lymphatic transport of triglycerides was about 20-fold greater and transport of apoprotein A-I was about twofold greater in fat-infused rats than in the other two groups. In each group transport of apoprotein A-I bore a significant positive relationship to transport of triglycerides. Lymphatic transport of the arginine-rich apoprotein was only 6-12% of that of apoprotein A-I and was more closely related to lymphatic transport of total protein than to that of triglycerides. In fat-infused rats given [(3)H]lysine intraduodenally, about two-thirds of the (3)H in the chylomicron proteins was in apoprotein A-I and only about 1% was in the arginine-rich apoprotein. Estimated specific activity of chylomicron proteins was highest for apoprotein A-I and apoprotein A-IV, and lowest for the arginine-rich apoprotein and proteins of low molecular weight (mainly C apoproteins). In fat-infused rats given constant intravenous infusions of radioiodinated high density lipoproteins from blood plasma, the specific activity of apoprotein A-I in lymph chylomicrons was only about 5% of that of apoprotein A-I in blood high density lipoproteins, indicating that more than 90% of the apoprotein A-I in chylomicrons was synthesized in the intestine. From these and other data it is concluded that both the intestine and liver are significant sources of apoprotein A-I whereas only the liver synthesizes significant amounts of the arginine-rich apoprotein.

摘要

在给大鼠进行十二指肠持续输注生理盐水、盐水中的葡萄糖或乳化脂肪后,检测了载脂蛋白A-I和富含精氨酸的载脂蛋白在肠系膜淋巴中的转运情况。在开始输注后的5至50小时内,所有组的淋巴流量保持恒定。与其他两组相比,输注脂肪的大鼠中甘油三酯的淋巴转运量大约高20倍,载脂蛋白A-I的转运量大约高两倍。在每组中,载脂蛋白A-I的转运与甘油三酯的转运呈显著正相关。富含精氨酸的载脂蛋白的淋巴转运量仅为载脂蛋白A-I的6%-12%,并且与总蛋白的淋巴转运关系更为密切,而非甘油三酯。在十二指肠内给予[(3)H]赖氨酸的输注脂肪的大鼠中,乳糜微粒蛋白中约三分之二的(3)H存在于载脂蛋白A-I中,而在富含精氨酸的载脂蛋白中仅约1%。乳糜微粒蛋白的估计比活性对于载脂蛋白A-I和载脂蛋白A-IV最高,而对于富含精氨酸的载脂蛋白和低分子量蛋白(主要是C载脂蛋白)最低。在给输注脂肪的大鼠持续静脉输注来自血浆的放射性碘化高密度脂蛋白后,淋巴乳糜微粒中载脂蛋白A-I的比活性仅约为血液高密度脂蛋白中载脂蛋白A-I比活性的5%,这表明乳糜微粒中超过90%的载脂蛋白A-I是在肠道中合成的。从这些以及其他数据可以得出结论,肠道和肝脏都是载脂蛋白A-I的重要来源,而只有肝脏合成大量富含精氨酸的载脂蛋白。

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