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接受促红细胞生成素治疗的血液透析患者红细胞中嘌呤核苷酸浓度和酶活性的变化

Changed purine nucleotide concentrations and enzyme activities in erythrocytes of haemodialysis patients undergoing erythropoietin therapy.

作者信息

Siems W, Grune T, Hampl H, Wendel G, Gerber G, Riedel E

机构信息

Institut für Biochemie, Charité, Humboldt-Universität zu Berlin.

出版信息

Eur J Clin Chem Clin Biochem. 1992 Aug;30(8):455-60. doi: 10.1515/cclm.1992.30.8.455.

Abstract

Therapy of renal anaemia in haemodialysis patients with chronic renal failure by application of recombinant human erythropoietin leads to an increase of the haematocrit. Rejuvenation of the erythrocyte population results in a decrease of the median density (D50), an increase of cell age-dependent enzyme activities, such as aspartate aminotransferase, and elevated concentrations of purine nucleotides in the erythrocytes. After density gradient separation of erythrocyte populations into cell age-dependent fractions, the concentrations of adenosine-5'-triphosphate, guanosine-5'-triphosphate and guanosine-5'-diphosphate were be found to be elevated by 25-100% in all cell fractions from haemodialysis patients, compared with a healthy control group. Therapy of haemodialysis patients with recombinant human erythropoietin leads to further increase (65%) of ATP in the younger (low density) cells, but not in the older (high density) cells. The elevated concentrations of ATP and total adenine nucleotides during recombinant human erythropoietin therapy possibly result in improved deformability of erythrocytes. The data point to an enhancement of the proportion of younger erythrocytes, but not to an improvement of the reduced life span of erythrocytes of haemodialysis patients during therapy with recombinant human erythropoietin.

摘要

应用重组人促红细胞生成素治疗慢性肾衰竭血液透析患者的肾性贫血会导致血细胞比容增加。红细胞群体的年轻化会导致中位密度(D50)降低、细胞年龄依赖性酶活性增加,如天冬氨酸氨基转移酶,以及红细胞中嘌呤核苷酸浓度升高。将红细胞群体通过密度梯度分离成细胞年龄依赖性组分后,发现与健康对照组相比,血液透析患者所有细胞组分中的三磷酸腺苷、三磷酸鸟苷和二磷酸鸟苷浓度升高了25% - 100%。用重组人促红细胞生成素治疗血液透析患者会使较年轻(低密度)细胞中的三磷酸腺苷进一步增加(65%),但较老(高密度)细胞中则不会。重组人促红细胞生成素治疗期间三磷酸腺苷和总腺嘌呤核苷酸浓度升高可能会导致红细胞变形性改善。数据表明较年轻红细胞的比例增加,但在重组人促红细胞生成素治疗期间血液透析患者红细胞缩短的寿命并未得到改善。

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