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采用31P-NMR监测疲劳的代谢和非代谢成分。

Metabolic and nonmetabolic components of fatigue monitored with 31P-NMR.

作者信息

Baker A J, Carson P J, Miller R G, Weiner M W

机构信息

Department of Medicine, University of California, San Francisco 94121.

出版信息

Muscle Nerve. 1994 Sep;17(9):1002-9. doi: 10.1002/mus.880170907.

Abstract

The goal of this study was to determine the roles of metabolic and nonmetabolic factors in muscle fatigue. Rat gastrocnemius muscles were fatigued by stimulation of the nerve (n = 6) or muscle (n = 4, after 2 days of denervation). 31Phosphorus nuclear magnetic resonance spectroscopy was used to measure levels of intracellular inorganic phosphate (Pi) and hydrogen ions (H+) (which are thought to inhibit contraction) and the high-energy phosphates, phosphocreatine (PCr), and ATP. For both indirect and direct stimulation, with fatigue to approximately 60% initial tetanic force, [Pi] increased from approximately 3.5 mmol/L to approximately 20 mmol/L and [PCr] decreased from approximately 27 mmol/L to approximately 9 mmol/L. However, with continued fatigue to 25-35% initial tetanic force, neither [Pi] or [PCr] changed further. [ATP] and pH changed only slightly during fatigue. The results are consistent with early fatigue arising from metabolic inhibition of contraction; but later fatigue arising independent of metabolites, due to impaired activation beyond the neuromuscular junction.

摘要

本研究的目的是确定代谢和非代谢因素在肌肉疲劳中的作用。通过刺激神经(n = 6)或肌肉(去神经支配2天后,n = 4)使大鼠腓肠肌疲劳。采用31磷核磁共振波谱法测量细胞内无机磷酸盐(Pi)和氢离子(H+)(被认为可抑制收缩)以及高能磷酸盐、磷酸肌酸(PCr)和三磷酸腺苷(ATP)的水平。对于间接和直接刺激,当疲劳至初始强直收缩力的约60%时,[Pi]从约3.5 mmol/L增加至约20 mmol/L,[PCr]从约27 mmol/L降至约9 mmol/L。然而,当持续疲劳至初始强直收缩力的25 - 35%时,[Pi]和[PCr]均未进一步变化。[ATP]和pH在疲劳过程中仅略有变化。结果表明,早期疲劳源于收缩的代谢抑制;但后期疲劳独立于代谢产物产生,是由于神经肌肉接头以外的激活受损所致。

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