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大鼠载脂蛋白A-IV的代谢

Metabolism of apolipoprotein A-IV in rat.

作者信息

Ghiselli G, Crump W L, Musanti R, Sherrill B C, Gotto A M

机构信息

Baylor College of Medicine, Houston, TX.

出版信息

Biochim Biophys Acta. 1989 Nov 6;1006(1):26-34. doi: 10.1016/0005-2760(89)90319-6.

Abstract

The metabolism of apolipoprotein A-IV (apo-IV) has been investigated in the rat. In this animal species, apoA-IV is a major protein constituent of plasma HDL and lymph chylomicron. The apolipoprotein is also present in the lipoprotein-deficient fraction (LDF) of plasma and lymph. In vivo studies with the radioiodinated protein showed the apoA-IV does not exchange freely between HDL and LDF and that LDF apoA-IV had a faster catabolism than HDL apoA-IV. ApoA-IV in chylomicrons is a direct precursor of apoA-IV in plasma HDL but not of that in LDF. On the other hand lymph LDF apoA-IV is an important precursor of plasma LDF apoA-IV. Transfer of apoA-IV from plasma to lymph is negligible, and since most of apoA-IV in lymph is present in LDF, we speculate that LDF apoA-IV is the major apoA-IV secretory product of the intestine. Studies aimed at identifying the site of catabolism of apoA-IV utilizing either radioiodinated or [14C]sucrose labelled apoA-IV, gave results consistent with the view that the liver plays a major role. When tested, human apoA-IV behaved in vivo in rat as the autologous protein. These findings, together with others previously published (Ghiselli, G. et al. (1987) J. Lipid Res. 27, 813-827), support the conclusion that the plasma metabolism of apoA-IV is remarkably similar in rat and human. We speculate that in mammals the rapid plasma catabolism of apoA-IV is mediated by an efficient uptake by the liver.

摘要

已在大鼠中研究了载脂蛋白A-IV(apo-IV)的代谢。在这种动物物种中,apoA-IV是血浆高密度脂蛋白(HDL)和淋巴乳糜微粒的主要蛋白质成分。该载脂蛋白也存在于血浆和淋巴的脂蛋白缺陷组分(LDF)中。用放射性碘化蛋白进行的体内研究表明,apoA-IV在HDL和LDF之间不能自由交换,并且LDF中的apoA-IV比HDL中的apoA-IV具有更快的分解代谢。乳糜微粒中的apoA-IV是血浆HDL中apoA-IV的直接前体,但不是LDF中apoA-IV的直接前体。另一方面,淋巴LDF中的apoA-IV是血浆LDF中apoA-IV的重要前体。apoA-IV从血浆向淋巴的转移可忽略不计,并且由于淋巴中大多数apoA-IV存在于LDF中,我们推测LDF中的apoA-IV是肠道主要的apoA-IV分泌产物。利用放射性碘化或[14C]蔗糖标记的apoA-IV来确定apoA-IV分解代谢部位的研究结果与肝脏起主要作用的观点一致。经测试,人apoA-IV在大鼠体内的行为与自身蛋白相同。这些发现与之前发表的其他研究结果(Ghiselli, G.等人,(1987年)《脂质研究杂志》27卷,813 - 827页)一起,支持了apoA-IV在大鼠和人类中的血浆代谢非常相似的结论。我们推测,在哺乳动物中,apoA-IV在血浆中的快速分解代谢是由肝脏的有效摄取介导的。

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