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Kinetics of the inhibition of the Na-K pump by external sodium.

机译:外部钠对Na-K泵抑制的动力学。

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摘要

1. When the ouabain-sensitive K influx or the ouabain-sensitive Cs influx is measured as a function of the extracellular concentration of K or Cs in Na-free solutions the resulting saturation curve at first rises more rapidly than a rectangular hyperbola, i.e. the curve is antisigmoid. 2. If the ouabain-sensitive K influx or the ouabain-sensitive Cs influx is measured in Na-free solutions at a fixed low concentration of K or Cs and at varying concentrations of Li, the influx decreases monotonically as the Li concentration rises and there is no evidence of competitive activation. 3. These findings can be accounted for by a model which proposes that there are two binding sites for K or Cs and that both the singly loaded and doubly loaded pump is capable of transport. 4. Extracellular Na changes the shape of both the K and the Cs saturation curve from antisigmoid to sigmoid. Dixon plots (1/ouabain-sensitive influx versus Na concentration at fixed K or Cs concentration) are linear at intermediate concentrations of K or Cs. 5. Na does not change the rate of K influx if the measurements are made at nearly saturating K concentrations using cells with nearly saturating internal Na concentrations. The effect of outside Na cannot therefore be explained by any mechanism which requires that Na alter the Vmax of the pump. 6. Measurement of the ouabain-sensitive Cs influx as a function of the external Cs concentration in solutions with different fixed Na concentrations results in curves which change from antisigmoid in Na-free solutions to sigmoid as the Na concentration rises. Dixon plots are linear at all but the lowest and highest Cs concentrations. 7. The resulting curves are best fit by equations which result from a model which proposes that Na acts both as a dead-end competitive inhibitor and as a heterotropic allosteric effector. Simpler models which propose either that Na acts solely as a dead-end competitive inhibitor or as a heterotropic allosteric effector do not fit as well as the more complicated model. 8. The combined competitive inhibition and allosteric effector model also describes adequately the relation between the ouabain-sensitive K influx and external K concentration measured at different external Na concentrations.
机译:1.当在无钠溶液中对哇巴因敏感的K涌入或哇巴因敏感的Cs涌入作为细胞外K或Cs浓度的函数进行测量时,所产生的饱和度曲线首先比矩形双曲线更快地上升,即曲线是反乙状结肠。 2.如果在无钠溶液中以固定的低K或Cs浓度和不同的Li浓度测量了哇巴因敏感的K流入量或哇巴因敏感的Cs流入量,则随着Li浓度的增加,流入量单调减少。尚无竞争激活的证据。 3.这些发现可以由一个模型解释,该模型提出存在两个K或Cs结合位点,并且单载和双载泵都能够运输。 4.细胞外Na将K和Cs饱和曲线的形状从反乙状结肠变为乙状结肠。 Dixon图(在固定的K或Cs浓度下,1 /哇巴因敏感的入渗量与Na浓度)在中等浓度的K或Cs下呈线性关系。 5.如果使用内部Na浓度接近饱和的电池以接近饱和的K浓度进行测量,则Na不会改变K的流入速率。因此,外部Na的影响无法通过任何需要Na改变泵的Vmax的机制来解释。 6.在具有不同固定Na浓度的溶液中,哇巴因敏感的Cs涌入量作为外部Cs浓度的函数,其测量曲线随Na浓度的升高从无Na溶液中的抗乙状结肠变为乙状结肠。除最低和最高Cs浓度外,狄克逊图在所有情况下都是线性的。 7.所得曲线最适合由一个模型得出的方程拟合,该方程表明Na既充当末端竞争性抑制剂,又充当异质变构效应物。较简单的模型提出了Na只能单独充当末端竞争性抑制剂或异向性变构效应子的说法,但并不适合较复杂的模型。 8.竞争抑制和变构效应子模型的组合还充分描述了哇巴因敏感的K流入量与在不同外部Na浓度下测得的外部K浓度之间的关系。

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