Mainwood G W, Renaud J M, Mason M J
Can J Physiol Pharmacol. 1987 Apr;65(4):648-58. doi: 10.1139/y87-108.
Following a period of intense repetitive stimulation (e.g., brief tetanic stimuli every second for 3 min), muscle isometric tension development is reduced by about 80%. This suppression is reversible at a high external pH (8.0) with a half time of 15-20 min, but if the external pH is low (6.4) or the buffer concentration is low, recovery is prevented. Inhibition of recovery is associated with a slowed rate of lactate loss, which may suggest that intracellular lactacidosis is the cause of the inhibition. Alternatively, a low external pH may affect recovery from fatigue quite independently of its effect on lactate efflux. The possibility that surface membrane properties are changed by fatigue in a pH-dependent fashion was examined by measuring the cable properties and action potentials of fatigued fibres at different external pH values. A low external pH during recovery from fatigue was shown to result in a prolonged membrane depolarization of 10-12 mV, an increased transmembrane resistance, and a prolonged action potential. At a high external pH transmembrane resistance is lowered by fatigue, the depolarization lasts only about 10-15 min, and there is a smaller effect on the action potential. While the fatigued fibre membrane does show a changed response that is dependent on external pH, it is not clear that this could be related to the suppression of contraction. Direct measurements of intracellular pH show a fall of about 0.4 to 0.5 pH units in the surface fibres following fatigue. This results from the lactic acid generated during activity. It is now clear that lactate crosses the membrane in association with protons and at least part of this flux is mediated by a specific carrier mechanism. Efflux is limited by the transmembrane pH gradient, which in turn depends on the extracellular buffer concentration in the diffusion limited space around the fibres. Intracellular lactacidosis in resting muscles can be generated by a reversal of the normal flux. Fibres can be loaded with lactate (L) by increasing the extracellular [H+][L-] product with a resultant fall in intracellular pH. Lactate loads similar to those seen in fatigued muscle simulate some but not all of the responses seen in the postfatigue state. The twitch is prolonged with a slow relaxation phase, an increased time to peak tension but with an increase in peak tension. The effects are reversible but usually result in a reduced contractile response following the washout.(ABSTRACT TRUNCATED AT 400 WORDS)
在一段强烈的重复刺激(例如,每秒进行短暂强直刺激,持续3分钟)之后,肌肉等长张力的发展降低约80%。这种抑制在高外部pH值(8.0)时是可逆的,半衰期为15 - 20分钟,但如果外部pH值低(6.4)或缓冲液浓度低,则恢复受到阻碍。恢复的抑制与乳酸流失速率减慢有关,这可能表明细胞内乳酸酸中毒是抑制的原因。或者,低外部pH值可能相当独立于其对乳酸外流的影响而影响疲劳恢复。通过测量不同外部pH值下疲劳纤维的电缆特性和动作电位,研究了表面膜特性是否以pH依赖的方式因疲劳而改变。结果表明,疲劳恢复期间的低外部pH值会导致膜去极化延长10 - 12 mV、跨膜电阻增加以及动作电位延长。在高外部pH值时,疲劳会降低跨膜电阻,去极化仅持续约10 - 15分钟,对动作电位的影响较小。虽然疲劳纤维膜确实表现出依赖于外部pH值的变化反应,但尚不清楚这是否与收缩抑制有关。细胞内pH值的直接测量显示,疲劳后表面纤维的pH值下降约0.4至0.5个单位。这是由活动期间产生的乳酸所致。现在清楚的是,乳酸与质子一起穿过膜,并且这种通量至少部分是由特定的载体机制介导的。外流受跨膜pH梯度限制,而跨膜pH梯度又取决于纤维周围扩散受限空间中的细胞外缓冲液浓度。静息肌肉中的细胞内乳酸酸中毒可通过正常通量的逆转产生。通过增加细胞外[H + ][L - ]产物,使纤维加载乳酸(L),从而导致细胞内pH值下降。与疲劳肌肉中所见类似的乳酸负荷模拟了疲劳后状态下所见反应的一部分但不是全部。单收缩延长,舒张期缓慢,达到峰值张力的时间增加,但峰值张力增加。这些影响是可逆的,但冲洗后通常会导致收缩反应降低。(摘要截断于400字)