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Enregistrement W2061370383 · doi:10.1113/jphysiol.2013.258566

‘SIT’ down and relax: the interpolated twitch technique is still a valid measure of central fatigue during sustained contraction tasks

2013· letter· en· W2061370383 sur OpenAlexaff
Arthur J. Cheng, Brian H. Dalton, Brad Harwood, Geoffrey A. Power

Notice bibliographique

RevueThe Journal of Physiology · 2013
Typeletter
Langueen
DomaineEngineering
ThématiqueMuscle activation and electromyography studies
Établissements canadiensUniversity of CalgaryUniversity of British Columbia
Organismes subventionnairesnon disponible
Mots-clésIsometric exerciseMuscle fatigueContraction (grammar)Muscle contractionLimitingMotor cortexElectromyographyAmplitudePhysical medicine and rehabilitationStimulus (psychology)StimulationMathematicsPhysicsChemistryNeuroscienceMedicinePsychologyAnatomyPhysical therapyInternal medicineEngineering

Résumé

récupéré en direct d'OpenAlex

The interpolated twitch technique is a practical method used to determine whether impairments in voluntary drive are a limiting factor in the reduction of muscle contractile force during and following fatiguing efforts. This method has been validated and is extensively employed in neuromuscular research, although its accuracy has been questioned (Taylor, 2009). The principal component of the technique is that if an electrically evoked maximal twitch (SIT) elicits extra force when superimposed upon a maximal voluntary isometric contraction (MVC), this may represent the extent to which voluntary drive is impaired. Thus, a fatigue-induced increase in SIT amplitude can be attributed to central fatigue (i.e. decreased volitional drive from the motor cortex to the skeletal muscle; Gandevia et al. 2013), which may be responsible in part for the fatigue-induced force loss. A fatigue-related increase in SIT force probably results from either activation of additional motor units or an increase in the instantaneous firing frequency of motor units to the muscle. Surprisingly, Place et al. (2008) observed that a relative fatigue-related increase in SIT amplitude also occurs during in vitro experiments. Specifically, in mouse single fibres, superimposed stimuli were applied every 2–3 s on repeated near-maximal fatiguing contractions that lasted ∼1–2 min. A relative increase in SIT was explained by a shift in the force elicited by 70 Hz constant frequency stimulation to the steep part of the force–Ca2+ relationship during fatigue. In other words, a small increase in myoplasmic free [Ca2+] ([Ca2+]i) with a superimposed stimulus results in a relatively larger increase in force compared with the plateau portion of the force–Ca2+ relationship. Recently, Gandevia et al. (2013), the paper under focus for this Journal Club discussion, evoked SITs during an involuntary sustained contraction at 30 Hz stimulation frequency lasting 1 min in the human adductor pollicis muscle. This stimulation frequency represented stable maximal in vivo motor unit firing rates in this particular muscle. Interestingly and in opposition to the single fibre model, the human adductor pollicis SIT amplitude progressively decreased until task failure. It could be suggested that the decrease in SIT amplitude throughout the fatigue task in the human adductor pollicis was caused by decreased membrane excitability, as indicated by impairments in the corresponding M-wave properties for the SIT, in particular the large decrease in M-wave amplitude. Because motor unit discharge rates typically decrease during a high-intensity fatigue task, it is possible that maintaining a high stimulation frequency (i.e. 30 Hz) throughout a sustained isometric effort exceeds the physiological capacity to propagate action potentials along the sarcolemma. Importantly, the main finding that SIT force does not increase with time during an involuntary tetanic contraction of a human muscle (Gandevia et al. 2013) was opposite to the finding from fatigued single mouse muscle fibres (Place et al. 2008) in which SIT amplitude increased progressively until task failure. Gandevia et al. (2013) argued that the force–[Ca2+]i relationship is unimportant to the assessment of central fatigue during sustained contractions performed in humans because impaired action potential propagation seems to occur upstream of the site of sarcoplasmic reticulum Ca2+ release. Thus, even large changes in the force–[Ca2+]i relationship would be masked by sarcolemmal or t-tubular membrane depolarization failure. The implication here is that when assessing central fatigue using the interpolated twitch technique during sustained voluntary contractions, fatigue-induced increases in SIT amplitude can largely be explained by central fatigue mechanisms when action propagation failure is evident. In contrast to a sustained contraction task, Place et al. (2008) used intermittent isometric contractions to induce fatigue of single muscle fibres. Tasks involving intermittent contractions do not necessarily exhibit fatigue-induced reductions in M-wave amplitude (Duchateau & Hainaut, 1985), because intermittent contractions may provide sufficient recovery of membrane excitability between subsequent contractions. Accordingly, increased SIT amplitudes were observed during fatigue induced by intermittent contractions in the study by Place et al. (2008). Furthermore, membrane excitability problems may not be the sole explanation for the decreased SIT during sustained contractions. In mammalian single fibres, it was shown during 12 s of sustained 100 Hz stimulation that force decreased rapidly to 10% of its initial value (Duty & Allen, 1994). The fast progression of force loss was due to decreased Ca2+ release and also by large decreases in myofibrillar Ca2+ sensitivity as the force–[Ca2+]i relationship during fatigue was shifted to the right of the unfatigued force–[Ca2+]i curve. This observation could be explained by a rapid accumulation of metabolites such as inorganic phosphate that greatly reduces myofibrillar Ca2+ sensitivity during a sustained contraction without rest intervals. Nonetheless, these data support the observation by Gandevia et al. (2013) that intramuscular mechanisms are more likely to decrease rather than increase SIT during a sustained fatiguing contraction. Gandevia et al. (2013) have presented strong evidence that the development of SIT force during a sustained fatiguing contraction is not of peripheral origin but is primarily a result of central fatigue. That is, the increase in SIT force reflects the failure to recruit some motor units or to discharge them fast enough. In instances in which sarcolemmal action potential propagation failure has not occurred, it cannot yet be ruled out that intramuscular factors do not affect SIT amplitude given that the interpolated twitch technique depends intrinsically on the properties of skeletal muscle to generate force. Therefore, it should be kept in perspective that both peripheral and central factors can contribute to SIT force depending on the fatigue task performed. Ultimately, we believe that the interpolated twitch technique remains a useful and practical tool to provide a qualitative assessment of central fatigue. We thank Professor Charles L. Rice for his helpful guidance in overseeing the preparation of this article.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,002
score de la tête « metaresearch » (Gemma)0,003
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Expérimental (laboratoire) · Signal consensuel: Expérimental (laboratoire)
GenreSignal candidat: Méthodes · Signal consensuel: aucune
Score de désaccord entre enseignants0,003
Score d'incertitude au seuil0,012

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0020,003
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0010,000
Bibliométrie0,0010,001
Études des sciences et des technologies0,0000,001
Communication savante0,0010,001
Science ouverte0,0010,001
Intégrité de la recherche0,0010,001
Charge utile insuffisante (le modèle a refusé de juger)0,0030,001

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,012
Tête enseignante GPT0,223
Écart entre enseignants0,211 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeExpérimental (laboratoire)
Domainenon disponible
GenreMéthodes

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations9
Publié2013
Routes d'admission1
Résumé présentoui

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