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May 1, 1988Proceedings of the National Academy of Sciences589 citationsOpen Access

Effect of Ca2+ on cross-bridge turnover kinetics in skinned single rabbit psoas fibers: implications for regulation of muscle contraction.

BBBernhard Brenner

Structured PICO

P
Population
Skinned single rabbit psoas fibers
I
Intervention
Ca2+ activation
C
Comparator
Different levels of Ca2+ activation
O
Outcome
Rate constant of force redevelopment (fapp + gapp)surrogate

Ca2+ regulates muscle contraction primarily by affecting the rate constant of transition from non-force-generating to force-generating states (fapp) in rabbit psoas fibers.

Abstract

The effect of Ca2+ upon the rate constant of force redevelopment following a period of isotonic shortening with immediate restretch to the starting sarcomere length was studied in rabbit psoas fibers at 5 degrees C. Control experiments support the assumption that the rate constant of force redevelopment represents isometric cross-bridge turnover kinetics (fapp + gapp), where fapp and gapp are the rate constants characterizing the transitions from the non-force-generating states to the force-generating states and back to the non-force-generating states, respectively. Parallel measurements of the rate constant of force redevelopment and of force, stiffness, and fiber ATPase during isometric contraction allow the effect of Ca2+ upon fapp and gapp to be determined. Analysis reveals that Ca2+ has a marked effect upon fapp, while gapp remains approximately unchanged. Furthermore, in the range above 25-30% of maximum Ca2+ activation, regulation of force, stiffness, and ATPase is mediated through changes in fapp. Below this range, however, it cannot be ruled out that, in addition, cross-bridges are also switched in and out of the turnover process ("recruitment"). As a consequence of regulation through turnover kinetics, both Ca2+ sensitivity and the slope of force-pCa (-logCa2+) relations are shown to be affected by the ratio fapp/gapp, which may represent an important mechanism of modulation of contractile function in addition to modulation through changes within the regulatory protein system.

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Cite This Study

Bernhard Brenner (1988) studied this question.

synapsesocial.com/papers/6a15fc1bd9ab26d82ed14827https://doi.org/10.1073/pnas.85.9.3265
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