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细胞外钠离子对钠钾泵抑制作用的动力学

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

作者信息

Sachs J R

出版信息

J Physiol. 1977 Jan;264(2):449-70. doi: 10.1113/jphysiol.1977.sp011677.

Abstract
  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.
摘要
  1. 当在无钠溶液中测量哇巴因敏感的钾流入或哇巴因敏感的铯流入作为细胞外钾或铯浓度的函数时,所得的饱和曲线起初比矩形双曲线上升得更快,即曲线呈反S形。2. 如果在无钠溶液中,在固定的低钾或低铯浓度以及不同的锂浓度下测量哇巴因敏感的钾流入或哇巴因敏感的铯流入,随着锂浓度的升高,流入量单调下降,且没有竞争性激活的证据。3. 这些发现可以用一个模型来解释,该模型提出存在两个钾或铯的结合位点,并且单负载和双负载的泵都能够进行转运。4. 细胞外钠将钾和铯的饱和曲线形状从反S形变为S形。狄克逊图(在固定的钾或铯浓度下,1/哇巴因敏感的流入量与钠浓度的关系)在中等钾或铯浓度下是线性的。5. 如果在使用内部钠浓度接近饱和的细胞、在接近饱和的钾浓度下进行测量,钠不会改变钾流入的速率。因此,外部钠的作用不能用任何要求钠改变泵的Vmax的机制来解释。6. 在具有不同固定钠浓度的溶液中,测量哇巴因敏感的铯流入作为外部铯浓度的函数,得到的曲线从无钠溶液中的反S形变为随着钠浓度升高而变为S形。狄克逊图在除最低和最高铯浓度外的所有浓度下都是线性的。7. 所得曲线最适合由一个模型推导的方程,该模型提出钠既作为终末竞争性抑制剂又作为异促变构效应剂起作用。提出钠仅作为终末竞争性抑制剂或作为异促变构效应剂起作用的更简单模型不如这个更复杂的模型拟合得好。8. 竞争性抑制和变构效应剂的组合模型也充分描述了在不同外部钠浓度下测量的哇巴因敏感的钾流入与外部钾浓度之间的关系。

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