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钠钾泵抑制和再激活过程中心脏浦肯野纤维的细胞内钠活性

The intracellular sodium activity of cardiac Purkinje fibres during inhibition and re-activation of the Na-K pump.

作者信息

Deitmer J W, Ellis D

出版信息

J Physiol. 1978 Nov;284:241-59. doi: 10.1113/jphysiol.1978.sp012539.

Abstract
  1. The intracellular Na activity, aiNa, of sheep heart Purkinje fibres was continuously monitored using Na+-sensitive glass micro-electrodes. The effects of removal and restoration of external K, and of application and removal of various cardioactive steroids, were investigated. 2. The aiNa increased in K-free solutions and rapidly recovered on addition of external K. The rate of this recovery depended on both the external K concentration, [K]o, and the aiNa. The rate of aiNa recovery was found to be half maximally activated at a [K]o of about 10 mM. If corrections are applied to allow for changes in the net passive Na influx at various [K]o, then this value is increased to approximately 12.5 mM. 3. At a given [K]o, there appeared to be a linear relationship between the rate of aiNa recovery and the level to which aiNa had increased in K-free solution (over the range of aiNa from 7.5 to 31 mM). 4. Addition of the cardioactive steroids strophanthidin, acetylstrophanthidin, actodigin (AY 22,241) or dihydro-ouabain produced rapid changes of aiNa. At low concentrations, these compounds sometimes produced a small decrease in aiNa, while at concentrations above 10(-7) M they produced a dose-dependent increase. 5. The effects on aiNa of both low and high concentrations of all these cardioactive steroids were readily reversible within 120 min. The time course of the aiNa recovery mainly depended on the concentration of the cardioactive steroid applied, and on the level to which aiNa had increased. 6. Upon addition of a cardioactive steroid (above 10(-7) M, aiNa at first increased almost linearly with time. The rates of such an increase were measured during this period at various cardioactive steroid concentrations and used to produce dose-response curves. The concentrations that produced a half-maximum rate of aiNa increase were near to 10(-6) M for strophanthidin and acetylstrophanthidin, but near to 10(-5) M for actodigin and dihydro-ouabain. 7. The mean maximum rate of aiNa increase produced by the addition of a high cardioactive steroid concentration was 0.49 +/- 0.17 mM/min (+/-S.D., n = 21). This would indicate a net passive Na influx into the cells of approximately 2.8 p-mole/cm2sec. 8. This maximum rate of aiNa increase could be achieved by the addition of 10(-5) M-strophanthidin or acetylstrophanthidin, but 10(-4) to 10(-3) M-actodigin or dihydro-ouabain was required to produce a similar rate of increase. 9. The addition of these high cardioactive steroid concentrations produced an initially rapid increase of aiNa. After 15-30 min this aiNa increase slowed considerably. The aiNa appeared to reach a 'plateau' within 2-4 hr at levels much below those predicted for a Na electrochemical equilibrium across the cell membrane.
摘要
  1. 使用对钠离子敏感的玻璃微电极持续监测绵羊心脏浦肯野纤维的细胞内钠离子活性(aiNa)。研究了去除和恢复细胞外钾离子以及应用和去除各种强心甾类药物的影响。2. 在无钾溶液中aiNa升高,加入细胞外钾离子后迅速恢复。这种恢复速率取决于细胞外钾离子浓度([K]o)和aiNa。发现aiNa恢复速率在[K]o约为10 mM时达到最大激活速率的一半。如果进行校正以考虑不同[K]o下净被动钠离子内流的变化,那么该值会增加到约12.5 mM。3. 在给定的[K]o下,aiNa恢复速率与在无钾溶液中aiNa升高的水平之间似乎存在线性关系(在aiNa从7.5到31 mM的范围内)。4. 加入强心甾类药物毒毛花苷、乙酰毒毛花苷、阿克托地苷(AY 22,241)或双氢哇巴因会使aiNa迅速变化。在低浓度时,这些化合物有时会使aiNa略有降低,而在浓度高于10(-7) M时,它们会产生剂量依赖性增加。5. 所有这些强心甾类药物的低浓度和高浓度对aiNa 的影响在120分钟内都很容易逆转。aiNa恢复的时间进程主要取决于所应用的强心甾类药物的浓度以及aiNa升高的水平。6. 加入强心甾类药物(浓度高于10(-7) M)后,aiNa起初几乎随时间呈线性增加。在此期间,在不同强心甾类药物浓度下测量这种增加的速率,并用于绘制剂量 - 反应曲线。毒毛花苷和乙酰毒毛花苷使aiNa增加速率达到最大值一半时的浓度接近10(-6) M,而阿克托地苷和双氢哇巴因则接近10(-5) M。7. 加入高浓度强心甾类药物产生的aiNa增加的平均最大速率为0.49 +/- 0.17 mM/分钟(+/-标准差,n = 21)。这表明钠离子净被动流入细胞的量约为2.8皮摩尔/平方厘米·秒。8. 加入10(-5) M毒毛花苷或乙酰毒毛花苷可实现aiNa增加的最大速率,但需要10(-4)至10(-3) M阿克托地苷或双氢哇巴因才能产生类似的增加速率。9. 加入这些高浓度强心甾类药物会使aiNa起初迅速增加。15 - 30分钟后,这种aiNa增加显著减缓。aiNa似乎在2 - 4小时内达到一个“平台期”,其水平远低于细胞膜上钠离子电化学平衡所预测的水平。

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