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铷、钠和哇巴因对大鼠红细胞中铷流入的相互作用。

Rubidium, sodium and ouabain interactions on the influx of rubidium in rat red blood cells.

作者信息

Beaugé L A, Ortíz O

出版信息

J Physiol. 1970 Oct;210(3):519-32. doi: 10.1113/jphysiol.1970.sp009224.

Abstract
  1. The activation curve of rubidium influx by external rubidium in rat red cells showed an inflexion at a concentration around 0.2 mM. This inflexion point was displaced to the right by ouabain.2. The removal of sodium from the external solution changed the characteristics of the activation curve of rubidium influx. At external rubidium below 0.5 mM the uptake increased whereas above that concentration there was marked reduction. Thus the sodium-free effect on rubidium uptake is dependent on the external rubidium concentration.3. With 0.25 mM rubidium, the relationship between increase of rubidium influx and reduction of external sodium followed a more or less exponential function. All the increment was ouabain-sensitive.4. With a rubidium concentration above 0.5 mM the reduction of the rubidium uptake, as sodium was removed, followed curves of complex shape. With 10 mM rubidium, when sodium was reduced from 5 mM to zero, there was an increase instead of a further reduction. These results suggest interactions of several effects.5. The ouabain sensitivity of the rubidium influx in rat red cells is smaller than in other systems studied up to now. The dose-response curve was shifted to the right as the rubidium concentration increased and a plateau was obtained with rubidium only below 1 mM at 10(-5)M ouabain. When plotted as a percentage of the maximal inhibition the points fell into the theoretical curve following a simple one reactant/one site reaction.6. Ouabain inhibition seems to be a complex function of at least three variables: the concentration of the glycoside, the concentration of sodium and the concentration of rubidium. When sodium was absent, 10 muM rubidium was able to prevent, to a great extent, the inhibition produced by 10(-5) and 10(-4)M ouabain.
摘要
  1. 大鼠红细胞中,外源性铷引起的铷内流激活曲线在浓度约0.2 mM处出现拐点。哇巴因使该拐点右移。

  2. 去除细胞外溶液中的钠会改变铷内流激活曲线的特征。当细胞外铷浓度低于0.5 mM时,摄取增加;而高于该浓度时则显著降低。因此,无钠对铷摄取的影响取决于细胞外铷浓度。

  3. 当铷浓度为0.25 mM时,铷内流增加与细胞外钠减少之间的关系大致呈指数函数。所有增加均对哇巴因敏感。

  4. 当铷浓度高于0.5 mM时,随着钠的去除,铷摄取的减少呈现复杂形状的曲线。当铷浓度为10 mM,钠从5 mM降至零时,摄取反而增加而非进一步减少。这些结果提示存在多种效应的相互作用。

  5. 大鼠红细胞中铷内流对哇巴因的敏感性低于迄今所研究的其他系统。随着铷浓度增加,剂量 - 反应曲线右移,在10⁻⁵M哇巴因存在时,仅在铷浓度低于1 mM时获得平台期。当以最大抑制百分比作图时,各点符合一个简单的单反应物/单位点反应的理论曲线。

  6. 哇巴因抑制似乎是至少三个变量的复杂函数:糖苷浓度、钠浓度和铷浓度。当无钠时,10 μM铷能够在很大程度上防止10⁻⁵M和10⁻⁴M哇巴因产生的抑制作用。

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本文引用的文献

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The sensitivity of the sodium pump to external sodium.钠泵对细胞外钠离子的敏感性。
J Physiol. 1967 Sep;192(1):175-88. doi: 10.1113/jphysiol.1967.sp008295.

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