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与齐夫综合征相关的短暂性溶血性贫血中的红细胞代谢

Red cell metabolism in transient haemolytic anaemia associated with Zieve's syndrome.

作者信息

Goebel K M

出版信息

Eur J Clin Invest. 1975 Feb;5(1):83-91. doi: 10.1111/j.1365-2362.1975.tb00432.x.

Abstract

Reversible haemolytic anaemia associated with decreased red cell half-life and reticulocytosis was studied in 10 patients with Zieve's syndrome. Since the underlying cause of the red cell destruction is as yet unknown, we determined the critical metabolic functions of the red cells in order to define the assumed intracorpuscular defect causing haemolysis. The glucose metabolizing enzymes had normal or raised values. - In view of the diminished ATP and raised 2,3-diphosphoglycerate (2.3 DPG) levels - a combination which suggests a pyruvate kinase (PK) deficiency - additional procedures were carried out in order to detect an abnormal activity of the red cell PK. Studies of biochemical properties of PK such as thermostability, Michaelis-Menten constants, and activation and inhibition tests brought results markedly deviating from the norm.-Fractions containing old cells particularly disclosed PK instability. A defective red cell matabolism resulted which was measurable through ATP-instability, altered glucose utilization and lactate production. - Experimental cell aging procedures led to a markedly decreased red cell metabolism. These assays revealed that mutations of PK-control mechanisms might be involved as factor triggering haemolytic anaemia of Zieve's syndrome.

摘要

对10例齐夫综合征患者进行了研究,这些患者存在与红细胞半衰期缩短和网织红细胞增多相关的可逆性溶血性贫血。由于红细胞破坏的根本原因尚不清楚,我们测定了红细胞的关键代谢功能,以确定假定的导致溶血的细胞内缺陷。葡萄糖代谢酶的值正常或升高。鉴于ATP减少和2,3-二磷酸甘油酸(2,3-DPG)水平升高——这种组合提示丙酮酸激酶(PK)缺乏——为检测红细胞PK的异常活性进行了额外的检查。对PK的生化特性进行研究,如热稳定性、米氏常数以及激活和抑制试验,结果明显偏离正常。特别是含有衰老细胞的部分显示出PK不稳定。导致了有缺陷的红细胞代谢,这可通过ATP不稳定、葡萄糖利用改变和乳酸产生来衡量。实验性细胞老化过程导致红细胞代谢明显降低。这些检测表明,PK控制机制的突变可能是引发齐夫综合征溶血性贫血的一个因素。

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