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兴奋诱导大鼠骨骼肌中钠钾泵的激活。

Excitation-induced activation of the Na(+)-K+ pump in rat skeletal muscle.

作者信息

Everts M E, Clausen T

机构信息

Institute of Physiology, Aarhus University, Denmark.

出版信息

Am J Physiol. 1994 Apr;266(4 Pt 1):C925-34. doi: 10.1152/ajpcell.1994.266.4.C925.

DOI:10.1152/ajpcell.1994.266.4.C925
PMID:8178965
Abstract

The stimulating effect of excitation on the Na(+)-K+ pump was characterized in measurements of 22Na efflux, intracellular Na+ content, 86Rb influx, and [3H]ouabain binding in isolated rat soleus muscle. Direct stimulation (10 V, 1 ms, 2 Hz) rapidly increased 22Na efflux and 86Rb influx about twofold. These effects were blocked by tetracaine and ouabain, were not associated with any significant increase in intracellular Na+, and could not be attributed to a rise in extracellular K+. The stimulation of 22Na efflux was unaffected by tubocurarine, dantrolene, trifluoperazine, or bumetanide. Stimulation at 2 Hz increased the rate of [3H]ouabain binding by approximately 120% within 1 min, indicating an early specific activation of the Na(+)-K+ pump. Stimulation at 60 Hz for 10 s increased intracellular Na+ content by 58%. Reextrusion of Na+ was complete in 2 min and could be prevented by ouabain (10(-4) M) or by cooling to 0 degrees C. It is concluded that, in rat soleus muscle, excitation leads to a rapid and pronounced (up to 15-fold) stimulation of the Na(+)-K+ pump, even at modest increases in intracellular Na+. This activation mechanism may be essential for the maintenance of transmembrane Na(+)-K+ gradients and prompt recovery of excitability during contractile activity.

摘要

在对分离的大鼠比目鱼肌进行的22Na外流、细胞内Na+含量、86Rb内流以及[3H]哇巴因结合的测量中,对兴奋对钠钾泵的刺激作用进行了表征。直接刺激(10V,1ms,2Hz)迅速使22Na外流和86Rb内流增加约两倍。这些效应被丁卡因和哇巴因阻断,与细胞内Na+的任何显著增加无关,也不能归因于细胞外K+的升高。22Na外流的刺激不受筒箭毒碱、丹曲林、三氟拉嗪或布美他尼的影响。2Hz刺激在1分钟内使[3H]哇巴因结合率增加约120%,表明钠钾泵早期特异性激活。60Hz刺激10秒使细胞内Na+含量增加58%。2分钟内Na+的再排出完成,可被哇巴因(10-4M)或冷却至0℃阻止。得出的结论是,在大鼠比目鱼肌中,即使细胞内Na+适度增加,兴奋也会导致钠钾泵快速且显著(高达15倍)的刺激。这种激活机制对于维持跨膜钠钾梯度以及在收缩活动期间迅速恢复兴奋性可能至关重要。

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