Literature DB >> 10555062

Do cross-bridges contribute to the tension during stretch of passive muscle?

U Proske1, D L Morgan.   

Abstract

The tension rise during stretch of passive skeletal muscle is biphasic, with an initial steep rise, followed by a subsequent more gradual change. The initial rise has been interpreted as being due to the presence of numbers of long-term, stable cross-bridges in resting muscle fibres. A point of weakness with the cross-bridge interpretation is that the initial stiffness reaches its peak value at muscle lengths beyond the optimum for myofilament overlap. To explain this result it has been suggested that despite the reduced overlap at longer lengths, the closer interfilament spacing and a higher sensitivity of the myofilaments to Ca2+ allows more stable cross-bridges to form. Recently the stretch responses of passive muscle have been re-examined and it has been suggested that it is not necessary to invoke cross-bridge mechanisms at all. Explanations based on a viscous resistance to interfilament sliding and mechanical properties of the elastic filaments, the gap filaments, were thought to adequately account for the observed tension changes. However, an important property of passive muscle, the dependence of stretch responses on the immediate history of contraction and length changes, thixotropy, cannot be explained simply in terms of viscous and viscoelastic properties. The review discusses the cross-bridge interpretation of muscle thixotropy and the relationship of passive stiffness to filament resting tension and latency relaxation. It is proposed that cross-bridges can exist in three states; one, responsible for the resting stiffness, requires resting levels of calcium. When, during activation, calcium levels rise, cross-bridges enter a low-force, high-stiffness state, signalled by latency relaxation, before they move to the third, force-generating state. It is concluded that, compared with viscoelastic models, a cross-bridge-based explanation of passive muscle properties is better able to accommodate the currently known facts although, as new information becomes available, this view may need to be revised.

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Year:  1999        PMID: 10555062     DOI: 10.1023/a:1005573625675

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  44 in total

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Journal:  Am J Physiol       Date:  1997-07

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Journal:  J Physiol       Date:  1995-01-15       Impact factor: 5.182

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  48 in total

1.  A thixotropic effect in contracting rabbit psoas muscle: prior movement reduces the initial tension response to stretch.

Authors:  K S Campbell; R L Moss
Journal:  J Physiol       Date:  2000-06-01       Impact factor: 5.182

2.  History-dependent mechanical properties of permeabilized rat soleus muscle fibers.

Authors:  Kenneth S Campbell; Richard L Moss
Journal:  Biophys J       Date:  2002-02       Impact factor: 4.033

3.  Passive mechanical properties of the medial gastrocnemius muscle of the cat.

Authors:  N P Whitehead; J E Gregory; D L Morgan; U Proske
Journal:  J Physiol       Date:  2001-11-01       Impact factor: 5.182

4.  Do cross-bridges contribute to the tension during stretch of passive muscle? A response.

Authors:  G Mutungi; K W Ranatunga
Journal:  J Muscle Res Cell Motil       Date:  2000-04       Impact factor: 2.698

5.  Cardiac titin: molecular basis of elasticity and cellular contribution to elastic and viscous stiffness components in myocardium.

Authors:  Wolfgang A Linke; Julio M Fernandez
Journal:  J Muscle Res Cell Motil       Date:  2002       Impact factor: 2.698

6.  Lengthening but not shortening history of paraspinal muscle spindles in the low back alters their dynamic sensitivity.

Authors:  Dong-Yuan Cao; Joel G Pickar
Journal:  J Neurophysiol       Date:  2010-11-03       Impact factor: 2.714

7.  Muscle spindle signals combine with the sense of effort to indicate limb position.

Authors:  J A Winter; T J Allen; U Proske
Journal:  J Physiol       Date:  2005-08-18       Impact factor: 5.182

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Authors:  Dilson E Rassier; Eun-Jeong Lee; Walter Herzog
Journal:  Biol Lett       Date:  2005-09-22       Impact factor: 3.703

9.  A structural origin of latency relaxation in frog skeletal muscle.

Authors:  Naoto Yagi
Journal:  Biophys J       Date:  2006-10-06       Impact factor: 4.033

10.  Time course for the development of muscle history in lumbar paraspinal muscle spindles arising from changes in vertebral position.

Authors:  Weiqing Ge; Joel G Pickar
Journal:  Spine J       Date:  2007-07-19       Impact factor: 4.166

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