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疾病状态下血浆中的肠道型碱性磷酸酶

Intestinal variant alkaline phosphatase in plasma in disease.

作者信息

Kuwana T, Rosalki S B

机构信息

Department of Chemical Pathology and Human Metabolism, Royal Free Hospital, London, U.K.

出版信息

Clin Chem. 1990 Nov;36(11):1918-21.

PMID:1700741
Abstract

We investigated by enzyme electrophoresis after prolonged neuraminidase treatment the activity of "intestinal variant" (alpha 2-globulin mobility) alkaline phosphatase (EC 3.1.3.1; ALP) in the plasma of 189 patients selected for disorders (diabetes mellitus, liver cirrhosis, and chronic renal failure) with a known high frequency of increased plasma intestinal (beta-globulin mobility) ALP activity. The overall frequency of the variant ALP was 23.8%, whereas in the samples showing intestinal ALP it was 45.0%. The variant ALP was not observed in the absence of intestinal ALP, nor in patients of blood group A. Its frequency did not differ significantly between the different patient groups. Quantification of the variant ALP by densitometry was unsatisfactory but the quantity could be estimated by subtracting the intestinal ALP activity measured by electrophoresis from the activity determined by immunoassay with monoclonal antibody that reacts with both the intestinal and the variant forms. This indicated median activity of 12 U/L for the variant, approximately equal to that of the concomitant intestinal ALP. From the effects of papain and bromelain treatments, we suggest that "intestinal variant" represents intestinal ALP with attached membrane-binding domain.

摘要

我们通过长时间神经氨酸酶处理后的酶电泳,研究了189例因患有糖尿病、肝硬化和慢性肾衰竭等疾病而入选的患者血浆中“肠道变异型”(α2球蛋白迁移率)碱性磷酸酶(EC 3.1.3.1;ALP)的活性,这些疾病已知血浆肠道型(β球蛋白迁移率)ALP活性升高的频率较高。变异型ALP的总体频率为23.8%,而在显示肠道型ALP的样本中为45.0%。在没有肠道型ALP的情况下未观察到变异型ALP,在A型血患者中也未观察到。其频率在不同患者组之间无显著差异。通过密度测定法对变异型ALP进行定量并不理想,但可以通过用与肠道型和变异型均反应的单克隆抗体免疫测定法所测定的活性减去电泳法测定的肠道型ALP活性来估计其含量。这表明变异型的中位活性为12 U/L,大约等同于伴随的肠道型ALP的活性。从木瓜蛋白酶和菠萝蛋白酶处理的效果来看,我们认为“肠道变异型”代表具有附着膜结合结构域的肠道型ALP。

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