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钠钾泵在大鼠骨骼肌细胞膜完整性丧失后恢复收缩性中的作用。

Role of Na,K pumps in restoring contractility following loss of cell membrane integrity in rat skeletal muscle.

作者信息

Clausen T, Gissel H

机构信息

Department of Physiology, University of Aarhus, DK-8000 Aarhus C, Denmark.

出版信息

Acta Physiol Scand. 2005 Mar;183(3):263-71. doi: 10.1111/j.1365-201X.2004.01394.x.

Abstract

BACKGROUND AND AIM

In skeletal muscles, electrical shocks may elicit acute loss of force, possibly related to increased plasma membrane permeability, induced by electroporation (EP). We explore the role of the Na(+),K(+) pumps in force recovery after EP.

METHODS

Isolated rat soleus or extensor digitorum longus (EDL) muscles were exposed to EP paradigms in the range 100-800 V cm(-1), and changes in tetanic force, Na(+),K(+) contents, membrane potential, (14)C-sucrose space and the release of the intracellular enzyme lactic acid dehydrogenase (LDH) were characterized. The effects of Na(+),K(+) pump stimulation or inhibition were followed.

RESULTS

Electroporation caused voltage-dependent loss of force, followed by varying rates and degrees of recovery. EP induced a reversible loss of K(+) and gain of Na(+), which was not suppressed by tetrodotoxin, but associated with increased (14)C-sucrose space and release of LDH. In soleus, EP at 500 V cm(-1) induced complete loss of force, followed by a spontaneous, partial recovery. Stimulation of active Na(+),K(+) transport by adrenaline, the beta(2)-agonist salbutamol, calcitonin gene-related peptide (CGRP) and dibutyryl cyclic AMP increased initial rate of force recovery by 183-433% and steady-state force level by 104-143%. These effects were blocked by ouabain (10(-3) m), which also completely suppressed spontaneous force recovery. EP caused rapid and marked depolarization, followed by a repolarization, which was accelerated by salbutamol. Also in EDL, EP caused complete loss of force, followed by a spontaneous partial recovery, which was markedly stimulated by salbutamol.

CONCLUSION

Electroporation induces reversible depolarization, partial rundown of Na(+),K(+) gradients, cell membrane leakage and loss of force. This may explain the paralysis elicited by electrical shocks. Na(+),K(+) pump stimulation promotes restoration of contractility, possibly via its electrogenic action. The major new information is that the Na(+),K(+) pumps are sufficient to compensate a simple mechanical leakage. This may be important for force recovery in leaky muscle fibres.

摘要

背景与目的

在骨骼肌中,电刺激可能引发力量的急性丧失,这可能与电穿孔(EP)诱导的质膜通透性增加有关。我们探究了钠钾泵在电穿孔后力量恢复中的作用。

方法

将分离的大鼠比目鱼肌或趾长伸肌(EDL)暴露于100 - 800 V/cm范围内的电穿孔模式下,对强直收缩力、钠钾含量、膜电位、¹⁴C - 蔗糖空间以及细胞内酶乳酸脱氢酶(LDH)的释放变化进行表征。观察钠钾泵刺激或抑制的效果。

结果

电穿孔导致电压依赖性的力量丧失,随后是不同速率和程度的恢复。电穿孔引起钾的可逆性丧失和钠的增加,这不受河豚毒素抑制,但与¹⁴C - 蔗糖空间增加和LDH释放相关。在比目鱼肌中,500 V/cm的电穿孔导致力量完全丧失,随后是自发的部分恢复。肾上腺素、β₂ - 激动剂沙丁胺醇、降钙素基因相关肽(CGRP)和二丁酰环磷酸腺苷刺激钠钾主动转运,使力量恢复的初始速率提高183 - 433%,稳态力量水平提高104 - 143%。这些作用被哇巴因(10⁻³ m)阻断,哇巴因也完全抑制了自发的力量恢复。电穿孔导致快速且显著的去极化,随后是复极化,沙丁胺醇加速了复极化过程。同样在趾长伸肌中,电穿孔导致力量完全丧失,随后是自发的部分恢复,沙丁胺醇显著刺激了这一恢复过程。

结论

电穿孔诱导可逆性去极化、钠钾梯度部分降低、细胞膜渗漏和力量丧失。这可能解释了电刺激引起的麻痹。钠钾泵刺激可能通过其生电作用促进收缩力的恢复。主要的新信息是钠钾泵足以补偿简单的机械渗漏。这可能对渗漏肌纤维中的力量恢复很重要。

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