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    A Re-examination of Calcium Activation in the Huxley Cross-Bridge Model

    Source: Journal of Biomechanical Engineering:;1997:;volume( 119 ):;issue: 001::page 20
    Author:
    G. I. Zahalak
    ,
    I. Motabarzadeh
    DOI: 10.1115/1.2796060
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: This paper investigates mathematical relations between models of calcium activation kinetics and Huxley-type models of cross-bridge dynamics in muscle. It is found that different calcium-activation schemes lead to the same form of generalized Huxley rate equation with calcium activation (∂n/∂t) − v (∂n/∂x) = rf(α − n) − gn if it is assumed that calcium–troponin interaction rates are fast compared to the rates of transition associated with force-generating cross-bridge states. Calcium affects cross-bridge dynamics by modifying the bonding rate f, but does not affect the number of interacting cross bridges α or the unbonding rate g; this occurs through the appearance in the equation of an activation factor, r, which is a pure function of sarcoplasmic free calcium concentration. In particular, it is shown that both the “tight-coupling” and “loose-coupling” calcium-activation schemes introduced by Zahalak and Ma [1] lead to the same rate equation with the same activation factor; the difference between them appears in the calcium mass-balance equation. While both of these activation models can be made to fit simple twitch and force-velocity data equally well, experimentally observed load-dependent shifts in the free calcium concentration are compatible with the tight-coupling scheme, but not with loose coupling.
    keyword(s): Dynamics (Mechanics) , Force , Bonding , Stress , Equations AND Muscle ,
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      A Re-examination of Calcium Activation in the Huxley Cross-Bridge Model

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    contributor authorG. I. Zahalak
    contributor authorI. Motabarzadeh
    date accessioned2017-05-08T23:52:50Z
    date available2017-05-08T23:52:50Z
    date copyrightFebruary, 1997
    date issued1997
    identifier issn0148-0731
    identifier otherJBENDY-25971#20_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/118330
    description abstractThis paper investigates mathematical relations between models of calcium activation kinetics and Huxley-type models of cross-bridge dynamics in muscle. It is found that different calcium-activation schemes lead to the same form of generalized Huxley rate equation with calcium activation (∂n/∂t) − v (∂n/∂x) = rf(α − n) − gn if it is assumed that calcium–troponin interaction rates are fast compared to the rates of transition associated with force-generating cross-bridge states. Calcium affects cross-bridge dynamics by modifying the bonding rate f, but does not affect the number of interacting cross bridges α or the unbonding rate g; this occurs through the appearance in the equation of an activation factor, r, which is a pure function of sarcoplasmic free calcium concentration. In particular, it is shown that both the “tight-coupling” and “loose-coupling” calcium-activation schemes introduced by Zahalak and Ma [1] lead to the same rate equation with the same activation factor; the difference between them appears in the calcium mass-balance equation. While both of these activation models can be made to fit simple twitch and force-velocity data equally well, experimentally observed load-dependent shifts in the free calcium concentration are compatible with the tight-coupling scheme, but not with loose coupling.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleA Re-examination of Calcium Activation in the Huxley Cross-Bridge Model
    typeJournal Paper
    journal volume119
    journal issue1
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.2796060
    journal fristpage20
    journal lastpage29
    identifier eissn1528-8951
    keywordsDynamics (Mechanics)
    keywordsForce
    keywordsBonding
    keywordsStress
    keywordsEquations AND Muscle
    treeJournal of Biomechanical Engineering:;1997:;volume( 119 ):;issue: 001
    contenttypeFulltext
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