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[不同形式溶血性贫血中红细胞群体的年龄组成、红细胞中的ATP和2,3-二磷酸甘油酸组成]

[Age composition of the erythrocyte population, ATP and 2,3-diphosphoglycerate composition in erythrocytes in different forms of hemolytic anemia].

作者信息

Luganova I S, Blinov M N, Abdulkadyrova A S

出版信息

Vopr Med Khim. 1978 Jul-Aug;24(4):499-505.

PMID:685194
Abstract

The total erythrocyte population was subdivided into three age groups using as criteria the stability of red blood cells to osmotic shock and the values of glucose-6-phosphate dehydrogenase (G6PD) activity. The "old" erythrocytes constituted about 8%, "mature"--87% and "young"--5% under normal conditions. In hereditary microspherocytosis 70% of erythrocytes possessed a decreased osmotic resistance and higher G6PD activity as compared with normal state. Two categories of erythrocytes was found among "young" cells in Marchiafava-Micheli disease; one of them possessed normal osmotic resistance, the other--decreased osmotic resistance. The age composition of the erythrocyte population was normal in functional hyperbilirubinemia. Content of ATP was decreased in erythrocytes of patients with hereditary microspherocytosis, it was increased in Marchiafava-Micheli disease and approached the normal level in patients with functional hyperbilirubinemia. Concentration of 2,3-diphosphoglycerate was similar to the normal level in erythrocytes of patients with functional hyperbilirubinemia; an inverse correlation was observed between contents of hemoglobin and of 2,3-diphosphoglycerate in blood of patients with hereditary microspherocytosis and with Marchiafava-Michel disease.

摘要

根据红细胞对渗透休克的稳定性以及葡萄糖-6-磷酸脱氢酶(G6PD)活性值,将红细胞总数细分为三个年龄组。在正常情况下,“老龄”红细胞约占8%,“成熟”红细胞占87%,“年轻”红细胞占5%。在遗传性球形红细胞增多症中,与正常状态相比,70%的红细胞渗透抵抗力降低,G6PD活性更高。在Marchiafava-Micheli病的“年轻”细胞中发现了两类红细胞;其中一类具有正常的渗透抵抗力,另一类渗透抵抗力降低。功能性高胆红素血症患者红细胞群体的年龄组成正常。遗传性球形红细胞增多症患者红细胞中的ATP含量降低,Marchiafava-Micheli病患者红细胞中的ATP含量增加,功能性高胆红素血症患者红细胞中的ATP含量接近正常水平。功能性高胆红素血症患者红细胞中的2,3-二磷酸甘油酸浓度与正常水平相似;在遗传性球形红细胞增多症患者和Marchiafava-Michel病患者的血液中,血红蛋白含量与2,3-二磷酸甘油酸含量呈负相关。

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