Literature DB >> 3597214

Role of intracellular pH in muscle fatigue.

J M Metzger, R H Fitts.   

Abstract

Intracellular pH of in vitro diaphragm preparations was determined following low- (5 Hz, 1.5 min) and high- (75 Hz, 1 min) frequency stimulation, using glass microelectrodes of the liquid membrane type (pHm). Results were compared with values obtained by the standard homogenate technique (pHh). High- and low-frequency stimulation reduced peak tetanic tension to 21 +/- 1 (SE) and 71 +/- 2% of initial values, respectively. Peak tetanic tension returned to resting values after 10- to 15-min recovery from high- or low-frequency stimulation. Resting pHm was 7.063 +/- 0.011 (n = 72), and after fatiguing stimulation declined to values as low as 6.33. During recovery pHm significantly increased and by 10 min had returned to prefatigue values. No difference was observed in the recovery of pHm between the low- and high-frequency stimulation groups (analysis of variance test, ANOVA), and in both groups pHm recovery was highly correlated to the recovery of peak tetanic tension (r = 0.94, P less than 0.001). Resting pHh was 7.219 +/- 0.023 (n = 13), which was significantly higher than the pHm value. In contrast to pHm, intracellular pHh was significantly higher during recovery from 75- vs. 5-Hz stimulation (P less than 0.05). For both groups pHh increased significantly with time and by 10 min returned to prestimulation values. The ANOVA test demonstrated that pHh values were significantly higher than pHm values during recovery from fatigue. The results from this study support our hypothesis that fatigue from both high- and low-frequency stimulation is at least partially due to the deleterious effects of intracellular acidosis on excitation-contraction coupling.

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Year:  1987        PMID: 3597214     DOI: 10.1152/jappl.1987.62.4.1392

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  17 in total

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3.  Influence of recovery mode (passive vs. active) on time spent at maximal oxygen uptake during an intermittent session in young and endurance-trained athletes.

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4.  Low cell pH depresses peak power in rat skeletal muscle fibres at both 30 degrees C and 15 degrees C: implications for muscle fatigue.

Authors:  S T Knuth; H Dave; J R Peters; R H Fitts
Journal:  J Physiol       Date:  2006-06-29       Impact factor: 5.182

5.  Depression of Ca2+ insensitive tension due to reduced pH in partially troponin-extracted skinned skeletal muscle fibers.

Authors:  J M Metzger; R L Moss
Journal:  Biophys J       Date:  1988-12       Impact factor: 4.033

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7.  Phosphate and acidosis act synergistically to depress peak power in rat muscle fibers.

Authors:  Cassandra R Nelson; Edward P Debold; Robert H Fitts
Journal:  Am J Physiol Cell Physiol       Date:  2014-09-03       Impact factor: 4.249

Review 8.  Factors affecting the rate of phosphocreatine resynthesis following intense exercise.

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9.  Ca++-sensitizing mutations in troponin, P(i), and 2-deoxyATP alter the depressive effect of acidosis on regulated thin-filament velocity.

Authors:  Thomas J Longyear; Matthew A Turner; Jonathan P Davis; Joseph Lopez; Brandon Biesiadecki; Edward P Debold
Journal:  J Appl Physiol (1985)       Date:  2014-03-20

10.  Effect of acute hypoxia on respiratory muscle fatigue in healthy humans.

Authors:  Samuel Verges; Damien Bachasson; Bernard Wuyam
Journal:  Respir Res       Date:  2010-08-11
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