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疲劳人体骨骼肌中舒张缓慢的代谢原因。

The metabolic causes of slow relaxation in fatigued human skeletal muscle.

作者信息

Cady E B, Elshove H, Jones D A, Moll A

机构信息

Department of Medicine, University College London, Rayne Institute.

出版信息

J Physiol. 1989 Nov;418:327-37. doi: 10.1113/jphysiol.1989.sp017843.

Abstract
  1. The relationship between slowing of relaxation and changes of intracellular pH and phosphorous metabolites has been examined in human skeletal muscle during the development of fatigue and subsequent recovery. Results obtained with normal subjects have been compared with those from a subject with myophosphorylase deficiency (MPD) who produced no H+ from glycolysis during exercise and therefore afforded the opportunity of assessing the role of H+ in the slowing of relaxation. 2. Subjects fatigued the first dorsal interosseous muscle in a stepwise fashion under ischaemic conditions, with intervals between the fatiguing contractions during which the relaxation rate was measured from brief tetanic contractions and the muscle phosphorous metabolites and pH were measured by nuclear magnetic resonance spectroscopy. 3. After 21 s maximal voluntary contraction under ischaemic conditions, relaxation in the MPD subject slowed to approximately 50% of the rate in the fresh muscle at a time when the intramuscular pH had not changed. This demonstrates that there is a mechanism causing slowing of relaxation that is independent of H+ accumulation. 4. The normal subjects showed a slow recovery of relaxation compared to the MPD subject when the circulation was restored. The main difference in the intracellular metabolite concentrations between MPD and normal subjects at this time was that, for the latter, the pH remained low (around 6.5) for at least 60 s after the circulation was restored. The results suggest that the slow recovery is a consequence of continuing acidosis, i.e. the existence of a pH-dependent mechanism of slowing. 5. The existence of a pH-dependent mechanism was further indicated by the fact that for the normal subjects, for a similar intracellular concentration of phosphocreatine, relaxation of the recovering muscle was approximately half that of the fatiguing muscle. This was at a time when the pH of the recovering muscle was 0.3-0.4 units less than in the partially fatigued muscle. 6. The results show that in normal muscle there are at least two processes that lead to slow relaxation in fatigued muscle: one due to H+ accumulation, the other being independent of H+.
摘要
  1. 在人体骨骼肌疲劳发展及随后恢复过程中,研究了松弛减慢与细胞内pH值及磷代谢物变化之间的关系。已将正常受试者的结果与一名肌磷酸化酶缺乏症(MPD)受试者的结果进行比较,该受试者在运动过程中糖酵解不产生H⁺,因此提供了评估H⁺在松弛减慢中作用的机会。2. 受试者在缺血条件下逐步使第一背侧骨间肌疲劳,在疲劳收缩之间的间隔期,通过短暂强直收缩测量松弛速率,并通过核磁共振波谱法测量肌肉磷代谢物和pH值。3. 在缺血条件下进行21秒最大自主收缩后,MPD受试者的松弛减慢至新鲜肌肉时速率的约50%,此时肌肉内pH值未发生变化。这表明存在一种导致松弛减慢的机制,该机制与H⁺积累无关。4. 恢复循环后,与MPD受试者相比,正常受试者的松弛恢复较慢。此时MPD受试者与正常受试者细胞内代谢物浓度的主要差异在于,对于后者,恢复循环后pH值至少60秒保持在较低水平(约6.5)。结果表明,恢复缓慢是持续酸中毒的结果,即存在pH依赖性的松弛减慢机制。5. 对于正常受试者,在磷酸肌酸细胞内浓度相似的情况下,恢复中的肌肉松弛约为疲劳肌肉的一半,这一事实进一步表明了pH依赖性机制的存在。此时恢复中肌肉的pH值比部分疲劳肌肉低0.3 - 0.4个单位。6. 结果表明,在正常肌肉中,至少有两个过程导致疲劳肌肉松弛减慢:一个是由于H⁺积累,另一个与H⁺无关。

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