首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Galactosamine-induced alpha 1-antitrypsin deficiency in rats. Alterations in plasma glycoproteins and alpha 1-antitrypsin carbohydrate composition.
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Galactosamine-induced alpha 1-antitrypsin deficiency in rats. Alterations in plasma glycoproteins and alpha 1-antitrypsin carbohydrate composition.

机译:半乳糖胺诱导的大鼠α1-抗胰蛋白酶缺乏症。血浆糖蛋白和α1-抗胰蛋白酶碳水化合物组成的改变。

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摘要

Administration of D-galactosamine (GalNH2) is known to produce alterations in plasma glycoprotein levels, including alpha 1-antitrypsin. The authors have studied the effects of GalNH2 on circulating protein bound carbohydrates and on the plasma concentrations of two alpha 1-antiproteases, transferrin, IgG, and albumin in rats. The alpha 1-antiproteases from GalNH2-treated rats were isolated and their molecular weight, isoelectric point, and carbohydrate composition compared with those of control rat alpha 1-antiproteases. Total plasma protein, albumin, and transferrin levels in the GalNH2-treated rats do not differ significantly from those of control rats. Plasma protein-bound carbohydrate is decreased significantly in the experimental animals, compared with controls: sialic acid decreased 60%, neutral sugars decreased 43%, and amino sugars decreased 38%. The concentrations of alpha 1-antitrypsin (AAT) and a higher molecular weight alpha 1-antiprotease designated AP2 are decreased by 79% and 38%, respectively. AAT isolated from the plasma of GalNH2-treated rats contains 2-3 fewer moles of sialic acid, 3 fewer moles of neutral sugar, and 2 fewer moles of amino sugar per mole of antiprotease than AAT isolated from controls. AP2 from GalNH2-treated rats contains 1 fewer mole each of sialic acid, neutral sugar, and amino sugar per mole of antiprotease than AP2 from controls. These alterations are similar to those seen in humans with genetically determined alpha 1-antiprotease deficiency.
机译:已知D-半乳糖胺(GalNH2)的使用会引起血浆糖蛋白水平(包括α1-抗胰蛋白酶)发生变化。作者研究了GalNH2对循环蛋白结合的碳水化合物以及大鼠中两种α1-抗蛋白酶,转铁蛋白,IgG和白蛋白的血浆浓度的影响。分离了经GalNH2处理的大鼠的α1-抗蛋白酶,与对照大鼠α1-抗蛋白酶相比,它们的分子量,等电点和碳水化合物组成。 GalNH2处理的大鼠的总血浆蛋白,白蛋白和转铁蛋白水平与对照大鼠无明显差异。与对照组相比,实验动物的血浆蛋白结合碳水化合物显着减少:唾液酸减少60%,中性糖减少43%,氨基糖减少38%。 α1-抗胰蛋白酶(AAT)和称为AP2的较高分子量α1-抗蛋白酶的浓度分别降低了79%和38%。与从对照中分离的AAT相比,从GalNH2处理的大鼠血浆中分离出的AAT所含的每摩尔抗蛋白酶含量少2-3摩尔唾液酸,3摩尔中性糖和2摩尔氨基糖。来自GalNH2处理的大鼠的AP2每摩尔抗蛋白酶中的唾液酸,中性糖和氨基糖分别比对照组的AP2少1摩尔。这些改变与在遗传上确定的α1-抗蛋白酶缺乏症的人类中所见相似。

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