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尿毒症患者血浆中胍类物质对尿毒症时胰岛素与红细胞受体结合的影响。

The effect of guanidino substances from uremic plasma on insulin binding to erythrocyte receptors in uremia.

作者信息

Rocić B, Breyer D, Granić M, Milutinović S

机构信息

Institute for Diabetes, Endocrinology and Metabolic Diseases, Medical Faculty University of Zagreb, Yugoslavia.

出版信息

Horm Metab Res. 1991 Oct;23(10):490-4. doi: 10.1055/s-2007-1003736.

Abstract

We have studied insulin binding to erythrocyte receptors in a group of 25 nonobese, nondiabetic uremic patients undergoing maintenance hemodialysis for 2-54 months and 14 healthy controls. Erythrocytes of predialyzed uremics bind significantly less insulin than control erythrocytes (p less than 0.01). Dialysis resulted in a rapid increase of insulin binding (p less than 0.001). The concentrations of plasma insulin and glucose remained essentially unchanged during 5-hour hemodialysis and did not significantly differ from the control values. The down regulation of insulin receptors in undialyzed patients in the presence of normal plasma insulin concentration indicates that factors other than insulin itself could be responsible for insulin receptor activity during uremia. The results demonstrated that creatinine, creatine and glycocyamine have a direct suppressive effect on insulin binding of postdialyzed plasma (p less than 0.05) in concentration of 1 mmol/l. This suggested that specific uremic toxins could play an important role in the mechanisms of altered insulin binding during hemodialysis. Despite the high concentration of these compounds in blood of uremics, the only common feature for these compounds is the presence of the guanidino group in the molecule.

摘要

我们研究了25名非肥胖、非糖尿病的尿毒症患者(接受维持性血液透析2至54个月)和14名健康对照者红细胞受体对胰岛素的结合情况。透析前尿毒症患者的红细胞结合胰岛素的能力明显低于对照红细胞(p<0.01)。透析导致胰岛素结合迅速增加(p<0.001)。在5小时的血液透析过程中,血浆胰岛素和葡萄糖浓度基本保持不变,且与对照值无显著差异。在血浆胰岛素浓度正常的情况下,未透析患者胰岛素受体下调表明,除胰岛素本身外,其他因素可能在尿毒症期间对胰岛素受体活性起作用。结果表明,肌酐、肌酸和胍基乙酸在浓度为1 mmol/l时对透析后血浆的胰岛素结合有直接抑制作用(p<0.05)。这表明特定的尿毒症毒素可能在血液透析期间胰岛素结合改变的机制中起重要作用。尽管这些化合物在尿毒症患者血液中的浓度很高,但这些化合物的唯一共同特征是分子中存在胍基。

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