首页> 外文期刊>Acta physiologica Scandinavica >Role of Na,K pumps in restoring contractility following loss of cell membrane integrity in rat skeletal muscle.
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Role of Na,K pumps in restoring contractility following loss of cell membrane integrity in rat skeletal muscle.

机译:Na,K泵在大鼠骨骼肌细胞膜完整性丧失后恢复收缩力中的作用。

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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.
机译:背景与目的:在骨骼肌中,电击可能引起电穿孔(EP)引起的急性力损失,这可能与质膜通透性增加有关。我们探讨了EP后,Na(+),K(+)泵在力恢复中的作用。方法:将孤立的大鼠比目鱼肌或趾长伸肌(EDL)的肌肉暴露于100-800 V cm(-1)范围内的EP范式下,并观察其强直肌力,Na(+),K(+)含量,膜电位的变化,表征了(14)C-蔗糖空间和细胞内酶乳酸脱氢酶(LDH)的释放。遵循Na(+),K(+)泵刺激或抑制作用。结果:电穿孔导致电压依赖性力的损失,其次是恢复速率和恢复程度的变化。 EP诱导了K(+)的可逆损失和Na(+)的增加,其不受河豚毒素抑制,但与(14)C-蔗糖空间增加和LDH释放有关。在比目鱼眼中,EP在500 V cm(-1)引起力的完全丧失,随后自发,部分恢复。刺激肾上腺素,β(2)-激动剂沙丁胺醇,降钙素基因相关肽(CGRP)和二丁酰环AMP的活性Na(+),K(+)转运,使最初的力量恢复率增加了183-433%,并且稳定状态的力量水平提高了104-143%。这些作用被哇巴因(10(-3)m)阻止,后者也完全抑制了自发力的恢复。 EP引起快速而明显的去极化,然后再极化,沙丁胺醇可加速极化。同样在EDL中,EP导致力量完全丧失,随后自发部分恢复,这被沙丁胺醇明显刺激。结论:电穿孔诱导可逆去极化,Na(+),K(+)梯度的部分减少,细胞膜泄漏和力的损失。这可以解释由电击引起的麻痹。 Na(+),K(+)泵刺激可能通过其电生成作用促进收缩力的恢复。最新的主要信息是,Na(+),K(+)泵足以补偿简单的机械泄漏。这对于恢复渗漏的肌肉纤维中的力可能很重要。

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