ArticleThe Journal of physiology1998
Changes in the maximum speed of shortening of frog muscle fibres early in a tetanic contraction and during relaxation.
Article in The Journal of physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
13 citing papers in PubMed.
- Potential role of passively increased muscle temperature on contractile function.European journal of applied physiology · 2022Review
- Post-activation Potentiation Versus Post-activation Performance Enhancement in Humans: Historical Perspective, Underlying Mechanisms, and Current Issues.Frontiers in physiology · 2019Review
- Article
- Large-scale models reveal the two-component mechanics of striated muscle.International journal of molecular sciences · 2008Article
- Complex myograph allows the examination of complex muscle contractions for the assessment of muscle force, shortening, velocity, and work in vivo.Biomedical engineering online · 2008Article
- Determinants of force rise time during isometric contraction of frog muscle fibres.The Journal of physiology · 2007Article
- Activation kinetics of skinned cardiac muscle by laser photolysis of nitrophenyl-EGTA.Biophysical journal · 2004Article
- Thin filament activation and unloaded shortening velocity of rabbit skinned muscle fibres.The Journal of physiology · 2003Article
- Titin-based contribution to shortening velocity of rabbit skeletal myofibrils.The Journal of physiology · 2002Article
- Synchronous oscillations of length and stiffness during loaded shortening of frog muscle fibres.The Journal of physiology · 2001Article
- Ca2+ dependence of loaded shortening in rat skinned cardiac myocytes and skeletal muscle fibres.The Journal of physiology · 2000Article
- Force-velocity and unloaded shortening velocity during graded potassium contractures in frog skeletal muscle fibres.Journal of muscle research and cell motility · 2000Article
- Rate of phosphate release after photoliberation of adenosine 5'-triphosphate in slow and fast skeletal muscle fibers.Biophysical journal · 1998Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. Isotonic shortening velocities at very light loads were examined in single fibres of the anterior tibialis muscle of the frog, Rana temporaria, using load-clamp recording and slack tests (temperature, 1-3 degrees C; initial sarcomere length, 2.25 microns). 2. Shortening velocities at very light loads (force-clamp recording) were found to be higher early in the rise of a tetanic contraction than during the plateau of the contraction. The upper limit of the load at which there was elevated shortening velocity early in the contraction was 1.5-5.4% of the maximum tetanic tension (Fo) depending on the particular fibre. 3. The maximum shortening velocity determined using the slack test method (Vo) was as much as 30% greater early in a contraction than at the tetanic plateau. Vo was elevated above the plateau level up to about 30 ms after the end of the latent period, which is equivalent to the time required for the force in an isometric contraction to rise to about 30% of Fo. Vo is depressed below the plateau value during relaxation at the cessation of stimulation. 4. Stimulation studies show that the cross-bridge model of Huxley (1957) predicts the maximum shortening velocity to be greater early in a contraction, when new actin binding sites are becoming activated and new cross-bridge connections are being formed rapidly, than during steady-state contraction. The elevated shortening velocity in the model is a consequence of new cross-bridges being formed in the pulling configuration, and there being a delay before the newly added bridges are dragged beyond their equilibrium position so they begin to retard shortening. The model also predicts that maximum shortening velocity should be depressed below the plateau level during early relaxation as cross-bridge binding sites are rapidly removed from the active population.
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