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Hemolytic anemia with impaired hexokinase activity

机译:溶血性贫血己糖激酶活性受损

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摘要

Analyses of key glycolytic intermediates in freshly drawn red cells from six related individuals suggest that decreased hexokinase activity underlies the hemolytic process in the two members with overt hemolysis. Low red cell glucose 6-phosphate (G6P) was observed not only in the anemic patients but in the presumptive heterozygotes as well and served as a useful marker for the presence of the trait. Hexokinase activity was labile in distilled water hemolysates but was only slightly low when protected by glucose, mercaptoethanol, and ethylenediaminetetraacetate (EDTA). Normal red cell hexokinase was demonstrated to be dependent on glucose for maintenance of activity after heating to 45°C. The cells of the proposita are unable to utilize glucose efficiently at glucose concentrations lower than 0.2 mmole/liter whereas normal cells maintain linear glucose consumption to at least 0.05 mM glucose. These qualitative abnormalities could result from the presence of a mutant hexokinase with an abnormally reactive sulfhydryl group and altered substrate affinity in the red cells of this kindred.
机译:对来自六个相关个体的新鲜吸取的红细胞中关键糖酵解中间产物的分析表明,己糖激酶活性降低是两个成员进行明显溶血的溶血过程的基础。低血红细胞葡萄糖6-磷酸(G6P)不仅在贫血患者中被观察到,而且在推测的杂合子中也被观察到,并且可以作为性状存在的有用标记。己糖激酶活性在蒸馏水溶解物中不稳定,但在葡萄糖,巯基乙醇和乙二胺四乙酸盐(EDTA)保护下,其活性仅稍低。正常的红细胞己糖激酶已证明在加热至45°C后依赖葡萄糖来维持活性。在低于0.2 mmole / L的葡萄糖浓度下,前体细胞无法有效利用葡萄糖,而正常细胞则将线性葡萄糖消耗维持在至少0.05 mM葡萄糖。这些定性异常可能是由于突变的己糖激酶的存在而引起的,该突变的己糖激酶具有异常的反应性巯基并且在这种红细胞中底物亲和力发生了变化。

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