Jacobasch G, Grieger M, Gerth C, Bier K
Acta Biol Med Ger. 1977;36(5-6):717-30.
Until now pyruvate kinase enzymopathies have been described only for red blood cells. On the basis of these results special structural properties of the erythrocyte PK was assumed, which are not yet totally established. PK defects may cause a nonspherocytic hemolytic anemia. This enzymopathy is characterized by a polymorphism, which is expressed in more than 5 different pathological variants. Up to now 16 cases of PK deficiency have ben diagnozed in the GDR. The following parameters are used for the characterization of the PK: the PEP-dependance, the inhibition by ATP and alanine, the specificity to nucleotides, the stability to temperature and urea and the maturation dependence. Two pathological variants of the PK with a decreased PEP-affinity are described. Furthermore the differences in the energy metabolism of the red blood cells of these two patients under aerobic and anaerobic conditions are discussed.
到目前为止,丙酮酸激酶酶病仅在红细胞中被描述。基于这些结果,推测红细胞丙酮酸激酶具有特殊的结构特性,但尚未完全确定。丙酮酸激酶缺陷可能导致非球形细胞溶血性贫血。这种酶病的特征是多态性,表现为5种以上不同的病理变体。到目前为止,民主德国已诊断出16例丙酮酸激酶缺乏症病例。以下参数用于丙酮酸激酶的表征:对磷酸烯醇式丙酮酸的依赖性、ATP和丙氨酸的抑制作用、对核苷酸的特异性、对温度和尿素的稳定性以及成熟依赖性。描述了两种磷酸烯醇式丙酮酸亲和力降低的丙酮酸激酶病理变体。此外,还讨论了这两名患者的红细胞在有氧和无氧条件下能量代谢的差异。