Clausen T, Gissel H
Department of Physiology, University of Aarhus, DK-8000 Aarhus C, Denmark.
Acta Physiol Scand. 2005 Mar;183(3):263-71. doi: 10.1111/j.1365-201X.2004.01394.x.
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.
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.
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.
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.
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。
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。
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。
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。