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Am J Physiol Heart Circ Physiol 288: H389-H399, 2005; doi:10.1152/ajpheart.00722.2003
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Analysis of hystereses in force length and force calcium relations

Yael Yaniv,1 Raphael Sivan,1 and Amir Landesberg2

1Department of Electrical Engineering and 2Department of Biomedical Engineering, Technion, Israel Institute of Technology, Haifa, Israel

Submitted 31 July 2003 ; accepted in final form 6 August 2004

Analysis of the hystereses in the force-length relationship at constant Ca2+ concentration and in the force-calcium relationship at constant sarcomere length (SL) provides insight into the mechanisms that control cross-bridge (XB) recruitment. The hystereses are related here to two mechanisms that regulate the number of strong XBs: the cooperativity, whereby the number of strong XBs determines calcium affinity, and the mechanical feedback, whereby the shortening velocity determines the duration for which the XBs are in the strong state. The study simulates the phenomena and defines the role of these feedbacks. The model that couples calcium kinetics with XB cycling was built on Simulink software (Matlab). Counterclockwise (CCW) hysteresis, wherein the force response lags behind the SL oscillations, at a constant calcium level, is obtained in the force-length plane when neglecting the mechanical feedback and accounting only for the cooperativity mechanism. Conversely, the force response precedes the SL oscillations, yielding a clockwise (CW) hysteresis when only the mechanical feedback is allowed to exist. In agreement with experimental observations, either CW or CCW hysteresis is obtained when both feedbacks coexist: CCW hystereses are obtained at low frequencies (<3 Hz), and the direction is reversed to CW at higher frequencies (>3 Hz). The cooperativity dominates at low frequencies and allows the muscle to adapt XB recruitment to slow changes in the loading conditions. The changeover frequency from CCW to CW hysteresis defines the velocity limit above which the muscle absorbs rather than generates energy. The hysteresis in the force-calcium relation is conveniently explained by the same cooperativity mechanism. We propose that a single cooperativity mechanism that depends on the number of strong XBs can explain the hystereses in the force-length as well as in the force-calcium relationships.

excitation-contraction coupling; regulated actin; work loop; force-length relationship



Address for reprint requests and other correspondence: A. Landesberg, Dept. of Biomedical Engineering, Technion-IIT, Haifa 32000, Israel (E-mail: amir{at}biomed.technion.ac.il)




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Am. J. Physiol. Heart Circ. Physiol.Home page
O. Tchaicheeyan and A. Landesberg
Regulation of energy liberation during steady sarcomere shortening
Am J Physiol Heart Circ Physiol, November 1, 2005; 289(5): H2176 - H2182.
[Abstract] [Full Text] [PDF]




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