Gordon E E, de Hartog M
J Gen Physiol. 1969 Nov;54(5):650-63. doi: 10.1085/jgp.54.5.650.
Cell membrane transport of K(+) stimulates the rate of glycolysis in Ehrlich ascites tumor cells. A study of the characteristics of this relationship indicates that the stimulation occurs under anaerobic as well as under aerobic conditions. The data suggest that glycolysis is stimulated by a K(+) transport mechanism that is coupled to Na(+) transport because the effect is blunted or abolished when the principal intracellular ion is lithium or choline. This stimulus to glycolysis is blocked by ouabain and ethacrynic acid, agents that have been shown to inhibit monovalent cation transport in erythrocytes. In contrast to the action of ouabain, glycolysis is inhibited by ethacrynic acid in Ehrlich ascites tumor cells in the absence of cell membrane K(+) transport. In studies with ghost-free hemolysates of human erythrocytes and with cytosol prepared from Ehrlich ascites tumor cells, ethacrynic acid significantly blocks lactate formation from fructose diphosphate demonstrating the direct inhibitory effect of this agent on one or more enzymes of the Embden-Meyerhof pathway. Since ethacrynic acid has no influence on lactate formation in intact erythrocytes utilizing an endogenous substrate, the presumptive site of inhibition is proximal to the 3-phosphoglycerate level.
钾离子的细胞膜转运可刺激艾氏腹水瘤细胞中的糖酵解速率。对这种关系特征的一项研究表明,这种刺激在无氧和有氧条件下均会发生。数据表明,糖酵解受到一种与钠离子转运偶联的钾离子转运机制的刺激,因为当主要细胞内离子为锂或胆碱时,这种效应会减弱或消失。这种对糖酵解的刺激被哇巴因和依他尼酸阻断,这两种试剂已被证明可抑制红细胞中的单价阳离子转运。与哇巴因的作用相反,在没有细胞膜钾离子转运的情况下,依他尼酸可抑制艾氏腹水瘤细胞中的糖酵解。在用无空泡人红细胞溶血产物和从艾氏腹水瘤细胞制备的细胞溶质进行的研究中,依他尼酸显著阻断了由果糖二磷酸形成乳酸的过程,证明了该试剂对糖酵解途径中一种或多种酶的直接抑制作用。由于依他尼酸对利用内源性底物的完整红细胞中的乳酸形成没有影响,推测的抑制位点在3-磷酸甘油酸水平附近。