Gumińska M, Wazewska-Czyzewska M
Clin Chim Acta. 1975 Oct 15;64(2):165-72. doi: 10.1016/0009-8981(75)90198-9.
It has been shown that in some cases of congenital non-spherocytic haemolytic anaemia (CNSHA) with pyruvate kinase deficiency, the primary defect may be related to diminished magnesium-stimulated ATPase activity, followed by elevation of the erythrocyte ATP level. ATP as the end product of glycolysis inhibits by negative feedback control the activities of key glycolytic enzymes involved in energy production, i.e. pyruvate kinase (PK) and phosphofructokinase (PFK). Erythrocyte-deficient PK, however, is insensitive to the stimulating effect of fructose 1,6-diphosphate (FDP), which is normally a positive effector of PK. Both competing effectors, i.e. ATP and FDP, seem to show specific interaction. PK, inactive in the presence of high concentrations of ATP, seems to lose its sensitivity to FDP. This effect persists until ATP molecules are present in excess. In vitro incubation of deficient PK with ATPase resulted in increased PK activity as well as in recovery of its sensitivity to the stimulating effect of FDP. The same effects were obtained in vivo by administering magnesium levulinate intravenously to CNSHA patients with PK deficiency. This may indicate that magnesium ions stimulate deficient ATPase activity and lead to diminution of ATP as a negative effector for other regulatory enzymes.
业已表明,在某些丙酮酸激酶缺乏的先天性非球形红细胞溶血性贫血(CNSHA)病例中,主要缺陷可能与镁刺激的ATP酶活性降低有关,随后红细胞ATP水平升高。作为糖酵解终产物的ATP通过负反馈控制抑制参与能量产生的关键糖酵解酶的活性,即丙酮酸激酶(PK)和磷酸果糖激酶(PFK)。然而,红细胞缺乏PK对1,6 - 二磷酸果糖(FDP)的刺激作用不敏感,而FDP通常是PK的正效应物。两种竞争性效应物,即ATP和FDP,似乎表现出特异性相互作用。在高浓度ATP存在下无活性的PK似乎失去了对FDP的敏感性。这种效应一直持续到ATP分子过量存在。用ATP酶对缺乏的PK进行体外孵育导致PK活性增加以及恢复其对FDP刺激作用的敏感性。通过给患有PK缺乏的CNSHA患者静脉注射乙酰丙酸镁,在体内也获得了相同的效果。这可能表明镁离子刺激缺乏的ATP酶活性并导致作为其他调节酶负效应物的ATP减少。