Literature DB >> 9518709

Changes in the maximum speed of shortening of frog muscle fibres early in a tetanic contraction and during relaxation.

R K Josephson1, K A Edman.   

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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Year:  1998        PMID: 9518709      PMCID: PMC2230787          DOI: 10.1111/j.1469-7793.1998.511bt.x

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  28 in total

1.  Non-hyperbolic force-velocity relationship in single muscle fibres.

Authors:  K A Edman; L A Mulieri; B Scubon-Mulieri
Journal:  Acta Physiol Scand       Date:  1976-10

2.  The force-velocity relationship in vertebrate muscle fibres at varied tonicity of the extracellular medium.

Authors:  K A Edman; J C Hwang
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

3.  Development of activation and rise of tension in an isometric tetanus.

Authors:  G Cecchi; F Colomo; V Lombardi; G Piazzesi
Journal:  Pflugers Arch       Date:  1979-07       Impact factor: 3.657

4.  The influence of calcium on shortening velocity of skinned frog muscle cells.

Authors:  R A Podolin; L E Ford
Journal:  J Muscle Res Cell Motil       Date:  1983-06       Impact factor: 2.698

5.  Effects of fatigue and altered pH on isometric force and velocity of shortening at zero load in frog muscle fibres.

Authors:  K A Edman; A R Mattiazzi
Journal:  J Muscle Res Cell Motil       Date:  1981-09       Impact factor: 2.698

6.  The variation in isometric tension with sarcomere length in vertebrate muscle fibres.

Authors:  A M Gordon; A F Huxley; F J Julian
Journal:  J Physiol       Date:  1966-05       Impact factor: 5.182

7.  The velocity of unloaded shortening and its relation to sarcomere length and isometric force in vertebrate muscle fibres.

Authors:  K A Edman
Journal:  J Physiol       Date:  1979-06       Impact factor: 5.182

8.  Force-velocity relation in normal and nitrate-treated frog single muscle fibres during rise of tension in an isometric tetanus.

Authors:  G Cecchi; F Colomo; V Lombardi
Journal:  J Physiol       Date:  1978-12       Impact factor: 5.182

9.  Development of force-velocity relation, stiffness and isometric tension in frog single muscle fibres.

Authors:  C Ambrogi-Lorenzini; F Colomo; V Lombardi
Journal:  J Muscle Res Cell Motil       Date:  1983-04       Impact factor: 2.698

10.  Force-velocity relation for frog muscle fibres: effects of moderate fatigue and of intracellular acidification.

Authors:  N A Curtin; K A Edman
Journal:  J Physiol       Date:  1994-03-15       Impact factor: 5.182

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  13 in total

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Journal:  J Physiol       Date:  2000-05-15       Impact factor: 5.182

2.  Synchronous oscillations of length and stiffness during loaded shortening of frog muscle fibres.

Authors:  K A Edman; N A Curtin
Journal:  J Physiol       Date:  2001-07-15       Impact factor: 5.182

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5.  Determinants of force rise time during isometric contraction of frog muscle fibres.

Authors:  K A P Edman; R K Josephson
Journal:  J Physiol       Date:  2007-02-15       Impact factor: 5.182

6.  Titin-based contribution to shortening velocity of rabbit skeletal myofibrils.

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Journal:  J Physiol       Date:  2002-04-01       Impact factor: 5.182

7.  Thin filament activation and unloaded shortening velocity of rabbit skinned muscle fibres.

Authors:  Carl A Morris; Larry S Tobacman; Earl Homsher
Journal:  J Physiol       Date:  2003-05-02       Impact factor: 5.182

8.  Force-velocity and unloaded shortening velocity during graded potassium contractures in frog skeletal muscle fibres.

Authors:  F Colomo; L Pizza; A Scialpi
Journal:  J Muscle Res Cell Motil       Date:  2000-01       Impact factor: 2.698

9.  Large-scale models reveal the two-component mechanics of striated muscle.

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10.  Complex myograph allows the examination of complex muscle contractions for the assessment of muscle force, shortening, velocity, and work in vivo.

Authors:  Niels Rahe-Meyer; Matthias Pawlak; Christian Weilbach; Wilhelm Alexander Osthaus; Hainer Ruhschulte; Cristina Solomon; Siegfried Piepenbrock; Michael Winterhalter
Journal:  Biomed Eng Online       Date:  2008-07-10       Impact factor: 2.819

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