A Mathematical Model of Muscle Containing Heterogeneous Half-Sarcomeres Exhibits Residual Force Enhancement

A skeletal muscle fiber that is stimulated to contract and then stretched from L1 to L2 produces more force after the initial transient decays than if it is stimulated at L2. This behavior has been well studied experimentally, and is known as residual force enhancement. The underlying mechanism remains controversial. We hypothesized that residual force enhancement could reflect mechanical interactions between heterogeneous half-sarcomeres. To test this hypothesis, we subjected a computational model of interacting heterogeneous half-sarcomeres to the same activation and stretch protocols that produce residual force enhancement in real preparations. Following a transient period of elevated force associated with active stretching, the model predicted a slowly decaying force enhancement lasting >30 seconds after stretch. Enhancement was on the order of 13% above isometric tension at the post-stretch muscle length, which agrees well with experimental measurements. Force enhancement in the model was proportional to stretch magnitude but did not depend strongly on the velocity of stretch, also in agreement with experiments. Even small variability in the strength of half-sarcomeres (2.1% standard deviation, normally distributed) was sufficient to produce a 5% force enhancement over isometric tension. Analysis of the model suggests that heterogeneity in half-sarcomeres leads to residual force enhancement by storing strain energy introduced during active stretch in distributions of bound cross-bridges. Complex interactions between the heterogeneous half-sarcomeres then dissipate this stored energy at a rate much slower than isolated cross-bridges would cycle. Given the variations in half-sarcomere length that have been observed in real muscle preparations and the stochastic variability inherent in all biological systems, half-sarcomere heterogeneity cannot be excluded as a contributing source of residual force enhancement.

[1]  B. Colombini,et al.  Non cross-bridge stiffness in skeletal muscle fibres at rest and during activity. , 2005, Advances in experimental medicine and biology.

[2]  B. Colombini,et al.  A non-cross-bridge stiffness in activated frog muscle fibers. , 2002, Biophysical journal.

[3]  B. C. Abbott,et al.  ABSTRACTS OF MEMOIRS RECORDING WORK DONE AT THE PLYMOUTH LABORATORY THE FORCE EXERTED BY ACTIVE STRIATED MUSCLE DURING AND AFTER CHANGE OF LENGTH , 2022 .

[4]  K. Campbell,et al.  A thixotropic effect in contracting rabbit psoas muscle: prior movement reduces the initial tension response to stretch , 2000, The Journal of physiology.

[5]  D L Morgan,et al.  The effect on tension of non‐uniform distribution of length changes applied to frog muscle fibres. , 1979, The Journal of physiology.

[6]  B. Colombini,et al.  Crossbridge properties during force enhancement by slow stretching in single intact frog muscle fibres , 2007, The Journal of physiology.

[7]  H. T. ter Keurs,et al.  Arrhythmogenic Ca(2+) release from cardiac myofilaments. , 2006, Progress in biophysics and molecular biology.

[8]  M. Noble,et al.  Residual force enhancement after stretch of contracting frog single muscle fibers , 1982, The Journal of general physiology.

[9]  J. Seidman,et al.  Effect of Cardiac Myosin Binding Protein-C on Mechanoenergetics in Mouse Myocardium , 2004, Circulation research.

[10]  Gaudenz Danuser,et al.  Single muscle fiber contraction is dictated by inter-sarcomere dynamics. , 2002, Journal of theoretical biology.

[11]  T. Robinson,et al.  The measurement and dynamic implications of thin filament lengths in heart muscle. , 1979, The Journal of physiology.

[12]  K W Ranatunga,et al.  Crossbridge and non‐crossbridge contributions to tension in lengthening rat muscle: force‐induced reversal of the power stroke , 2006, The Journal of physiology.

[13]  Kenneth S. Campbell,et al.  Interactions between Connected Half-Sarcomeres Produce Emergent Mechanical Behavior in a Mathematical Model of Muscle , 2009, PLoS Comput. Biol..

[14]  K W Ranatunga,et al.  Dynamic behaviour of half‐sarcomeres during and after stretch in activated rabbit psoas myofibrils: sarcomere asymmetry but no ‘sarcomere popping’ , 2006, The Journal of physiology.

[15]  Kenneth B. Campbell,et al.  Model representation of the nonlinear step response in cardiac muscle , 2010, The Journal of general physiology.

[16]  W Herzog,et al.  Residual force enhancement in skeletal muscle , 2006, The Journal of physiology.

[17]  M. Bartoo,et al.  Active tension generation in isolated skeletal myofibrils , 1993, Journal of Muscle Research & Cell Motility.

[18]  M. Noble,et al.  Enhancement of mechanical performance of striated muscle by stretch during contraction , 1992, Experimental physiology.

[19]  K. Edman The velocity of unloaded shortening and its relation to sarcomere length and isometric force in vertebrate muscle fibres. , 1979, The Journal of physiology.

[20]  Jachen Denoth,et al.  Half-sarcomere dynamics in myofibrils during activation and relaxation studied by tracking fluorescent markers. , 2006, Biophysical journal.

[21]  L. McLoon,et al.  Complex three-dimensional patterns of myosin isoform expression: differences between and within specific extraocular muscles , 1999, Journal of Muscle Research & Cell Motility.

[22]  R. Moss,et al.  Ablation of Cardiac Myosin-Binding Protein-C Accelerates Stretch Activation in Murine Skinned Myocardium , 2006, Circulation research.

[23]  W. Herzog,et al.  Force enhancement in single skeletal muscle fibres on the ascending limb of the force–length relationship , 2004, Journal of Experimental Biology.

[24]  H. Sugi,et al.  Tension changes during and after stretch in frog muscle fibres , 1972, The Journal of physiology.

[25]  A. Arner,et al.  Desmin filaments influence myofilament spacing and lateral compliance of slow skeletal muscle fibers. , 2005, Biophysical journal.

[26]  A. Huxley Muscle structure and theories of contraction. , 1957, Progress in biophysics and biophysical chemistry.

[27]  G. Piazzesi,et al.  The contractile response during steady lengthening of stimulated frog muscle fibres. , 1990, The Journal of physiology.

[28]  J. Denoth,et al.  Inter-Sarcomere Dynamics in Muscle Fibres , 2003 .

[29]  R. Horowits Passive force generation and titin isoforms in mammalian skeletal muscle. , 1992, Biophysical journal.

[30]  D L Morgan An explanation for residual increased tension in striated muscle after stretch during contraction , 1994, Experimental physiology.

[31]  W. Herzog,et al.  Residual force enhancement exceeds the isometric force at optimal sarcomere length for optimized stretch conditions. , 2008, Journal of applied physiology.

[32]  W Herzog,et al.  Force enhancement following stretch in a single sarcomere. , 2010, American journal of physiology. Cell physiology.

[33]  W Herzog,et al.  Residual force enhancement in myofibrils and sarcomeres , 2008, Proceedings of the Royal Society B: Biological Sciences.