Shortening-induced force depression is primarily caused by cross-bridges in strongly bound states

Journal of Biomechanics

Volumn 42, Issue 14, 2009, Pages 2336-2340

  Lee, Eun Jeong ^a   Herzog, Walter ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

BDM; Cross bridge theory; Force depression; Skeletal muscle fibers

Indexed keywords

BDM; BOUND STATE; CONSTANT VELOCITIES; CROSS-BRIDGE; CROSS-BRIDGE THEORY; DOSE-DEPENDENT MANNER; FORCE DEPRESSION; FROG MUSCLES; ISOMETRIC CONTRACTIONS; ISOMETRIC FORCE; KINETIC CONDITIONS; RESIDUAL FORCES; RINGER'S SOLUTION; SKELETAL MUSCLE FIBERS;

FIBERS;

MUSCLE;

DIACETYL OXIME; RINGER SOLUTION;

ANIMAL TISSUE; ARTICLE; CONCENTRATION RESPONSE; CONTROLLED STUDY; FROG; KINEMATICS; MUSCLE CELL; MUSCLE FORCE; MUSCLE ISOMETRIC CONTRACTION; MUSCLE STIFFNESS; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; CELLS, CULTURED; COMPUTER SIMULATION; ISOMETRIC CONTRACTION; MODELS, ANATOMIC; MODELS, BIOLOGICAL; MUSCLE, SKELETAL; RANA PIPIENS; SARCOMERES; STRESS, MECHANICAL;

EID: 70349448529     PISSN: 00219290     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jbiomech.2009.06.026     Document Type: Article

References (29)

1. Abbott B.C., and Aubert X.M. The force exerted by active striated muscle during and after change of length. J. Physiol. (London) 117 (1952) 77-86
2. Bagni M.A., Cecchi G., Colomo F., and Garzella P. Effects of 2,3-butanedione monoxime on the crossbridge kinetics in frog single muscle-fibers. J. Muscle Res. Cell Motil. 13 (1992) 516-522
3. Bullimore S.R., Leonard T.R., Rassier D.E., and Herzog W. History-dependence of isometric muscle force: effect of prior stretch or shortening amplitude. J. Biomech. 40 (2007) 1518-1524
4. Daniel T.L., Trimble A.C., and Chase P.B. Compliant realignment of binding sites in muscle: transient behaviour and mechanical tuning. Biophys J. 74 (1998) 1611-1621
5. De Ruiter C.J., de Haan A., Jones D.A., and Sargeant A.J. Shortening-induced force depression in human adductor pollicis muscle. J. Physiol. (London) 507.2 (1998) 583-591
6. De Ruiter C.J., and de Haan A. Shortening-induced depression of voluntary force in unfatigued and fatigued human adductor pollicis muscle. J. Appl. Physiol. 94 (2003) 69-74
7. Edman K.A.P., Caputo C., and Lou F. Depression of tetanic force induced by loaded shortening of frog muscle fibres. J. Physiol. (London) 466 (1993) 535-552
8. Ettema G.J., and Meijer K. Muscle contraction history: modified Hill versus an exponential decay model. Biol. Cybern. 83 6 (2000) 491-500
9. Granzier H.L., and Pollack G.H. Effect of active pre-shortening on isometric and isotonic performance of single frog muscle fibres. J. Physiol. 415 (1989) 299-327
10. Herrmann C., Wray J., Travers F., and Barman T. Effect of 2,3-butanedione monoxime on myosin and myofibrillar ATPases. An example of an uncompetitive inhibitor. Biochemistry 31 (1992) 12227-12232
11. Herzog W., and Leonard T.R. Depression of cat soleus forces following isokinetic shortening. J. Biomech. 30 9 (1997) 865-872
12. Herzog W., Leonard T.R., and Wu J.Z. The relationship between force depression following shortening and mechanical work in skeletal muscle. J. Biomech. 33 (2000) 659-668
13. Higuchi H., Yanagida T., and Goldman Y.E. Compliance of thin filaments in skinned fibers of rabbit skeletal muscle. Biophys. J. 69 (1995) 1000-1010
14. Horiuti K., Higuchi H., Umazume Y., Konishi M., Okazaki O., and Kurihara S. Mechanism of action of 2, 3-Butanedione 2-monoxime on contraction of frog skeletal-muscle fibers. J. Muscle Res. Cell Motil. 9 (1988) 156-164
15. Huxley A.F., and Simmons R.M. Proposed mechanism of force generation in striated muscle. Nature 233 (1971) 533-538
16. Huxley H.E., Stewart A., Sosa H., and Irving T. X-ray diffraction measurements of the extensibility of actin and myosin filaments in contracting muscles. Biophys. J. 67 (1994) 2411-2421
17. Josephson R.K., and Stokes D.R. Work-dependent deactivation of a crustacean muscle. J. Exp. Biol. 202 18 (1999) 2551-2565
18. Joumaa V., and Herzog W. Force depression in single myofibrils. Biophys. J. 94 (2008) 903-Plat
19. Julian F.J., and Sollins M.R. Variation of muscle stiffness with force at increasing speeds of shortening. J. Gen. Physiol. 66 (1975) 287-302
20. Kojima H., Ishijima A., and Yanagida T. Direct measurement of stiffness of single actin filaments with and without tropomyosin by in vitro nanomanipulation. Proc. Natl. Acad. Sci. USA 91 (1994) 12962-12966
21. Lee H.D., and Herzog W. Force depression following muscle shortening of voluntarily activated and electricallystimulated human adductor pollicis. J. Physiol. (London) 551 (2003) 993-1003
22. Maréchal G., and Plaghki L. The deficit of the isometric tetanic tension redeveloped after a release of frog muscle at a constant velocity. J. Gen. Physiol. 73 (1979) 453-467
23. Morgan D.L., Whitehead N.P., Wise A.K., Gregory J.E., and Proske U. Tension changes in the cat soleus muscle following slow stretch or shortening of the contracting muscle. J. Physiol. (London) 522.3 (2000) 503-513
24. Regnier M., Morris C., and Homsher E. Regulation of the cross-bridge transition from a weakly to strongly bound state in skinned rabbit muscle fibers. Am. J. Physiol. 269 (1995) C1532-C1539
25. Stuyvers B.D., McCulloch A.D., Guo J., Duff H.J., and ter Keurs H.E. Effect of stimulation rate, sarcomere length and Ca(2+) on force generation by mouse cardiac muscle. J. Physiol. 544 (2002) 817-830
26. Sugi H., and Tsuchiya T. Stiffness changes during enhancement and deficit of isometric force by slow length changes in frog skeletal muscle fibres. J. Physiol. (London) 407 (1988) 215-229
27. ter Keurs H.E.D.J., Iwazumi T., and Pollack G.H. The sarcomere length-tension relation in skeletal muscle. J. Gen. Physiol. 72 (1978) 565-592
28. Tesi C., Colomo F., Piroddi N., and Poggesi C. Characterization of the cross-bridge force-generating step using inorganic phosphate and BDM in myofibrils from rabbit skeletal muscles. J. Physiol. (London) 541.1 (2002) 187-199
29. Wakabayashi K., Sugimoto Y., Tanaka H., Ueno Y., Takezawa Y., and Amemiya Y. X-ray-diffraction evidence for the extensibility of actin and myosin-filaments during muscle-contraction. Biophys. J. 67 (1994) 2422-2435