The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.
Motor drive and metabolic responses during repeated submaximal contractions in humans
Abstract
Contractile failure during various types of exercise has been attributed to intramuscular metabolic changes. We examined the temporal changes in force-generating capacity and metabolic state during intermittent isometric contractions in humans. One-legged quadriceps contractions at 30% maximum voluntary contraction (MVC) were executed for 6 s, with 4 s of rest between. The decrease in force-generating capacity was tested from brief MVC's and short bursts of 50-Hz stimulation applied at 5-min intervals. After 1 min of exercise, the MVC force declined linearly and in parallel to the 50-Hz stimulation force, indicating that the contractile failure was due to intramuscular processes. After 30 min of exercise the MVC force had declined by approximately 40% compared with the value obtained after 1 min. In separate experiments the same contraction protocol was followed, but two-legged contractions were used. Muscle biopsies taken after 5, 15, and 30 min of exercise showed only minor changes in the concentrations of glycogen, lactate, creatine phosphate (CrP), and ATP. However, at exhaustion, defined as loss of ability to sustain the target force, the concentrations of CrP and glycogen were reduced by 73 and 32%, and muscle lactate concentration had increased to 4.8 mmol/kg wet wt. Thus the gradual decline in force-generating capacity was not due to lactacidosis or lack of substrates for ATP resynthesis and must have resulted from excitation/contraction coupling failure, whereas exhaustion was closely related to phosphagen depletion, without significant lactacidosis.
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“and (2) ®ndings to suggest that high-intensity intermittent exercise performed in a 5 s work/5 s recovery duty cycle is likely to be fuelled largely by muscle high-energy phosphate breakdown during work and resynthesis of high energy phosphates by oxidative phosphorylation during recovery (Edwards et al. 1973, Vollestad et al. 1988).”
From Slower fatigue and faster recovery of the adductor pollicis muscle in women matched for strength with men (1999) · cites this paper as Vollestad et al. 1988
Citations
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“Others also have observed similar relative reductions in voluntary and electrically evoked isometric torque after fatiguing tasks of the knee extensors (12,13) and adductor pollicis (12) muscles.”
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Metadata
- Authors
- Vollestad, N. K., Sejersted, O. M., Bahr, R., Woods, J. J., & Bigland-Ritchie, B.
- Venue
- Journal of Applied Physiology
- Publisher
- American Physiological Society
- Published
- 1988-04-01
- Volume
- 64
- Issue
- 4
- Pages
- 1421-1427
- ISSN
- 0161-7567 (ISSN-L)
- 8750-7587
- 1522-1601
- OpenAlex
- W2269573921
- Cited by
- 172
- References
- 20
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 1 · 2023: 2 · 2022: 1 · 2021: 3 · 2020: 1 · 2019: 5 · 2017: 3 · 2016: 1 · 2015: 3 · 2014: 3 · 2013: 4 · 2012: 5
- FWCI
- 13.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Applied Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL30062)
- National Institute of Neurological Disorders and Stroke (NS 14576)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Cardiovascular and exercise physiology
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Physical Sciences › Engineering › Biomedical Engineering › Muscle activation and electromyography studies
- Keywords
- contractile failure, excitation-contraction coupling, muscle fatigue, quadriceps, isometric contraction, force-generating capacity, muscle lactate, muscle glycogen, ATP resynthesis, exercise exhaustion, submaximal exercise, muscle metabolism
- MeSH terms
- Adenosine Triphosphate, Central Nervous System, Electric Stimulation, Energy Metabolism, Physical Exertion, Fatigue, Female, Glycogen, Humans, Isometric Contraction, Lactates, Male, Muscle Contraction, Muscles, Phosphocreatine
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