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. 1984 Feb;45(2):389–397. doi: 10.1016/S0006-3495(84)84163-6

Stiffness, force, and sarcomere shortening during a twitch in frog semitendinosus muscle bundles.

M Schoenberg, J B Wells
PMCID: PMC1434863  PMID: 6607749

Abstract

The time course of force and stiffness during a twitch was determined at 6 and 26 degrees C in frog semitendinosus muscle bundles using the transmission time technique of Schoenberg, M., J.B. Wells, and R.J. Podolsky, 1974, J. Gen. Physiol. 64:623-642. Sarcomere shortening due to series compliance was also measured using a laser light diffraction technique. Following stimulation, stiffness developed more rapidly than force, but had a slower time course than published Ca2+ transients determined from light signals using Ca2+ sensitive dyes (Baylor, S.M., W.K. Chandler, and M.W. Marshall, 1982, J. Physiol. (Lond.). 331:139-177). Stiffness (S) did not reach its tetanic value during a twitch at 6 or 26 degrees C, although at 6 degrees C, it approached close to this value with S-twitch/S-tetanus = 0.82 +/- 0.07 (+/- SEM). During relaxation, force fell more rapidly than stiffness both for a twitch and also a tetanus. Also in this paper, several of the assumptions inherent in using the transmission time technique for the measurement of stiffness are considered in detail.

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Selected References

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  1. ABBOTT B. C., RITCHIE J. M. The onset of shortening in striated muscle. J Physiol. 1951 Apr;113(2-3):336–345. doi: 10.1113/jphysiol.1951.sp004577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ashley C. C., Ridgway E. B. On the relationships between membrane potential, calcium transient and tension in single barnacle muscle fibres. J Physiol. 1970 Jul;209(1):105–130. doi: 10.1113/jphysiol.1970.sp009158. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baylor S. M., Chandler W. K., Marshall M. W. Use of metallochromic dyes to measure changes in myoplasmic calcium during activity in frog skeletal muscle fibres. J Physiol. 1982 Oct;331:139–177. doi: 10.1113/jphysiol.1982.sp014368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Blinks J. R., Rüdel R., Taylor S. R. Calcium transients in isolated amphibian skeletal muscle fibres: detection with aequorin. J Physiol. 1978 Apr;277:291–323. doi: 10.1113/jphysiol.1978.sp012273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Borejdo J., Mason P. Sarcomere length changes during stimulation of frog semitendinosus muscle. J Mechanochem Cell Motil. 1976 Mar;3(3):155–161. [PubMed] [Google Scholar]
  6. Bressler B. H., Clinch N. F. The compliance of contracting skeletal muscle. J Physiol. 1974 Mar;237(3):477–493. doi: 10.1113/jphysiol.1974.sp010493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cecchi G., Colomo F., Lombardi V. Force-velocity relation in normal and nitrate-treated frog single muscle fibres during rise of tension in an isometric tetanus. J Physiol. 1978 Dec;285:257–273. doi: 10.1113/jphysiol.1978.sp012570. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cecchi G., Griffiths P. J., Taylor S. Muscular contraction: kinetics of crossbridge attachment studied by high-frequency stiffness measurements. Science. 1982 Jul 2;217(4554):70–72. doi: 10.1126/science.6979780. [DOI] [PubMed] [Google Scholar]
  9. Civan M. M., Podolsky R. J. Contraction kinetics of striated muscle fibres following quick changes in load. J Physiol. 1966 Jun;184(3):511–534. doi: 10.1113/jphysiol.1966.sp007929. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Cleworth D. R., Edman K. A. Changes in sarcomere length during isometric tension development in frog skeletal muscle. J Physiol. 1972 Dec;227(1):1–17. doi: 10.1113/jphysiol.1972.sp010016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Close R. I. Activation delays in frog twitch muscle fibres. J Physiol. 1981;313:81–100. doi: 10.1113/jphysiol.1981.sp013652. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Ford L. E., Huxley A. F., Simmons R. M. Tension responses to sudden length change in stimulated frog muscle fibres near slack length. J Physiol. 1977 Jul;269(2):441–515. doi: 10.1113/jphysiol.1977.sp011911. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ford L. E., Huxley A. F., Simmons R. M. The relation between stiffness and filament overlap in stimulated frog muscle fibres. J Physiol. 1981 Feb;311:219–249. doi: 10.1113/jphysiol.1981.sp013582. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. González-Serratos H. Inward spread of activation in vertebrate muscle fibres. J Physiol. 1971 Feb;212(3):777–799. doi: 10.1113/jphysiol.1971.sp009356. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. HUXLEY A. F. Muscle structure and theories of contraction. Prog Biophys Biophys Chem. 1957;7:255–318. [PubMed] [Google Scholar]
  16. Hill D. K. Tension due to interaction between the sliding filaments in resting striated muscle. The effect of stimulation. J Physiol. 1968 Dec;199(3):637–684. doi: 10.1113/jphysiol.1968.sp008672. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hill T. L., Eisenberg E., Chen Y. D., Podolsky R. J. Some self-consistent two-state sliding filament models of muscle contraction. Biophys J. 1975 Apr;15(4):335–372. doi: 10.1016/S0006-3495(75)85823-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Huxley A. F., Simmons R. M. Proposed mechanism of force generation in striated muscle. Nature. 1971 Oct 22;233(5321):533–538. doi: 10.1038/233533a0. [DOI] [PubMed] [Google Scholar]
  19. Huxley H. E., Faruqi A. R., Kress M., Bordas J., Koch M. H. Time-resolved X-ray diffraction studies of the myosin layer-line reflections during muscle contraction. J Mol Biol. 1982 Jul 15;158(4):637–684. doi: 10.1016/0022-2836(82)90253-4. [DOI] [PubMed] [Google Scholar]
  20. JEWELL B. R., WILKIE D. R. An analysis of the mechanical components in frog's striated muscle. J Physiol. 1958 Oct 31;143(3):515–540. doi: 10.1113/jphysiol.1958.sp006075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Katz B. The relation between force and speed in muscular contraction. J Physiol. 1939 Jun 14;96(1):45–64. doi: 10.1113/jphysiol.1939.sp003756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Kawai M., Brandt P. W. Two rigor states in skinned crayfish single muscle fibers. J Gen Physiol. 1976 Sep;68(3):267–280. doi: 10.1085/jgp.68.3.267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kawai M., Brandt P., Orentlicher M. Dependence of energy transduction in intact skeletal muscles on the time in tension. Biophys J. 1977 May;18(2):161–172. doi: 10.1016/S0006-3495(77)85605-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Kobayashi T., Sugi H. Segmental length changes in stimulated frog sartorius muscle during dynamic mechanical responses. Jpn J Physiol. 1982;32(5):817–830. doi: 10.2170/jjphysiol.32.817. [DOI] [PubMed] [Google Scholar]
  25. Matsubara I., Yagi N. A time-resolved X-ray diffraction study of muscle during twitch. J Physiol. 1978 May;278:297–307. doi: 10.1113/jphysiol.1978.sp012305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Schoenberg M., Wells J. B., Podolsky R. J. Muscle compliance and the longitudinal transmission of mechanical impulses. J Gen Physiol. 1974 Dec;64(6):623–642. doi: 10.1085/jgp.64.6.623. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Stienen G. J., Blangé T. Local movement in stimulated frog sartorius muscle. J Gen Physiol. 1981 Aug;78(2):151–170. doi: 10.1085/jgp.78.2.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Yagi N., Ito M. H., Nakajima H., Izumi T., Matsubara I. Return of myosin heads to thick filaments after muscle contraction. Science. 1977 Aug 12;197(4304):685–687. doi: 10.1126/science.301660. [DOI] [PubMed] [Google Scholar]

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