Altamirano A A, Breitwieser G E, Russell J M
Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston 77550.
Am J Physiol. 1988 Apr;254(4 Pt 1):C582-6. doi: 10.1152/ajpcell.1988.254.4.C582.
The effects of vanadate and fluoride on the Na+-K+-Cl- cotransporter of the squid giant axon were assessed. In axons not treated with these agents, intracellular dialysis with ATP-depleting fluids caused bumetanide-inhibitable 36Cl influx to fall with a half time of approximately 16 min. In the presence of either 40 microM vanadate or 5 mM fluoride, the decay of bumetanide-inhibitable 36Cl influx was significantly slowed; half time for vanadate-treated axons is 45 min and for fluoride-treated axons is 37 min. These agents are not exerting their effects on Na+-K+-Cl- cotransport by influencing the rate of ATP depletion of the axon, since they had no effect on the ATP hydrolysis rate of an optic ganglia homogenate. We therefore suggest that these data support the hypothesis that Na+-K+-Cl- cotransport in squid axons is regulated by a phosphorylation-dephosphorylation mechanism and that vanadate and fluoride reduce the rate of dephosphorylation by inhibiting a protein phosphatase.
评估了钒酸盐和氟化物对枪乌贼巨大轴突钠钾氯共转运体的影响。在未用这些试剂处理的轴突中,用消耗ATP的液体进行细胞内透析会导致布美他尼抑制的36Cl内流下降,半衰期约为16分钟。在存在40 microM钒酸盐或5 mM氟化物的情况下,布美他尼抑制的36Cl内流的衰减明显减慢;钒酸盐处理的轴突半衰期为45分钟,氟化物处理的轴突半衰期为37分钟。这些试剂并非通过影响轴突ATP消耗速率来对钠钾氯共转运发挥作用,因为它们对视神经节匀浆的ATP水解速率没有影响。因此,我们认为这些数据支持以下假设:枪乌贼轴突中的钠钾氯共转运受磷酸化-去磷酸化机制调节,并且钒酸盐和氟化物通过抑制一种蛋白磷酸酶来降低去磷酸化速率。