Literature DB >> 306434

Filament sliding and energy absorbed by the cross-bridge in active muscle subjected to cycical length changes.

F W Flitney, D G Hirst.   

Abstract

1. The effects of single and double cycles of stretch and release on the tension response and relative sliding movement of the actin and myosin filaments in active frog's muscle were investigated. 2. The cross-bridges linking the filaments together are able to accommodate a greater range of filament displacement before becoming detached during a second cycle stretch, providing it commences without delay following the preceding release: sarcomere 'give' then occurs for displacements of around 18 nm, as compared with 12 nm for a first cycle stretch. It is postulated that the difference arises because the myosin heads adopt different 'preferred' positions in the isometric steady-state and at the end of a previous release. 3. Muscle length-tension loops were recorded and used to measure the energy absorbed when a muscle is subjected to cycles of stretch and release. The work absorbed per unit length change increases with increasing displacement of the cross-bridges from their initial (isometric) steady-state position, up to the point at which sarcomere 'give' occurs (S2); thereafter it remains constant. 4. More work is absorbed during the first cycle of a double stretch-release combination than during the second. The greater amount absorbed during the first cycle is associated with a correspondingly greater amount of filament sliding in the period following sarcomere 'give'. Sarcomere length-tension loops were constructed and these showed that not less than 80-85% of the work done on a muscle is absorbed by the sarcomeres themselves. 5. A greater amount of work is done on stretching up to (but not beyond) S2 during second cycle stretch as compared to a first. The difference amounts about 1 mJ.m-2 per half-sarcomere. 6. The results are compatible with the mechanism for force production proposed by Huxley & Simmons (1973), in which each myosin head generates force in a number of stepping movements, from one attached state to another. It is concluded that (a) during an unloaded isotonic contraction the working 'stroke' of the head would result in a 10-13 nm relative sliding movement of the filaments, and (b) the potential energy difference separating the two 'preferred' states is 6-9.6 kT per cross-bridge, or 3-4.8 kT per S-1 sub-units, assuming that each one interacts simultaneously with the actin filament.

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Year:  1978        PMID: 306434      PMCID: PMC1282438          DOI: 10.1113/jphysiol.1978.sp012247

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


  9 in total

1.  Use of an X-ray television for diffraction of the frog striated muscle.

Authors:  I Matsubara; N Yagi; H Hashizume
Journal:  Nature       Date:  1975-06-26       Impact factor: 49.962

2.  The instantaneous elasticity of frog skeletal muscle fibres [proceedings].

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1976-09       Impact factor: 5.182

3.  Cross-bridge detachment and sarcomere 'give' during stretch of active frog's muscle.

Authors:  F W Flitney; D G Hirst
Journal:  J Physiol       Date:  1978-03       Impact factor: 5.182

4.  X-ray evidence for radial cross-bridge movement and for the sliding filament model in actively contracting skeletal muscle.

Authors:  J C Haselgrove; H E Huxley
Journal:  J Mol Biol       Date:  1973-07-15       Impact factor: 5.469

Review 5.  The activation of striated muscle and its mechanical response.

Authors:  A F Huxley
Journal:  Proc R Soc Lond B Biol Sci       Date:  1971-06-15

6.  Muscular contraction.

Authors:  A F Huxley
Journal:  J Physiol       Date:  1974-11       Impact factor: 5.182

Review 7.  Recent x-ray diffraction studies of muscle.

Authors:  J Hanson
Journal:  Q Rev Biophys       Date:  1968-06       Impact factor: 5.318

8.  Mechanical properties of the cross-bridges of frog striated muscle.

Authors:  A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1971-10       Impact factor: 5.182

9.  Heat work and phosphorylcreatine break-down in muscle.

Authors:  D R Wilkie
Journal:  J Physiol       Date:  1968-03       Impact factor: 5.182

  9 in total
  20 in total

1.  Stiffness and tension during and after sudden length changes of glycerinated single insect fibrillar muscle fibres.

Authors:  K Güth; H J Kuhn; B Drexler; W Berberich; J C Rüegg
Journal:  Biophys Struct Mech       Date:  1979-08

2.  Millisecond-scale biochemical response to change in strain.

Authors:  Dale C Bickham; Timothy G West; Martin R Webb; Roger C Woledge; Nancy A Curtin; Michael A Ferenczi
Journal:  Biophys J       Date:  2011-11-15       Impact factor: 4.033

3.  Increased force levels after shortening and restretching skinned cardiac muscle.

Authors:  N M De Clerck
Journal:  J Muscle Res Cell Motil       Date:  1991-04       Impact factor: 2.698

4.  Effects of solution tonicity on crossbridge properties and myosin lever arm disposition in intact frog muscle fibres.

Authors:  Barbara Colombini; Maria Angela Bagni; Giovanni Cecchi; Peter John Griffiths
Journal:  J Physiol       Date:  2006-10-05       Impact factor: 5.182

5.  Crossbridge properties during force enhancement by slow stretching in single intact frog muscle fibres.

Authors:  Barbara Colombini; Marta Nocella; Giulia Benelli; Giovanni Cecchi; Maria Angela Bagni
Journal:  J Physiol       Date:  2007-10-11       Impact factor: 5.182

6.  Reversal of the myosin power stroke induced by fast stretching of intact skeletal muscle fibers.

Authors:  Barbara Colombini; Marta Nocella; Giulia Benelli; Giovanni Cecchi; Peter J Griffiths; M Angela Bagni
Journal:  Biophys J       Date:  2009-12-02       Impact factor: 4.033

7.  A cross-bridge mechanism can explain the thixotropic short-range elastic component of relaxed frog skeletal muscle.

Authors:  K S Campbell; M Lakie
Journal:  J Physiol       Date:  1998-08-01       Impact factor: 5.182

8.  Energetics of lengthening in mouse and toad skeletal muscles.

Authors:  J K Constable; C J Barclay; C L Gibbs
Journal:  J Physiol       Date:  1997-11-15       Impact factor: 5.182

9.  The contractile response during steady lengthening of stimulated frog muscle fibres.

Authors:  V Lombardi; G Piazzesi
Journal:  J Physiol       Date:  1990-12       Impact factor: 5.182

10.  Analysis of Ca2+ and Sr2+ activation characteristics in skinned muscle fibre preparations with different proportions of myofibrillar isoforms.

Authors:  G S Lynch; D G Stephenson; D A Williams
Journal:  J Muscle Res Cell Motil       Date:  1995-02       Impact factor: 2.698

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