Skip to main content
Log in

Fibre type transition and stiffness modification of soleus muscle of trained rats

  • Excitable Tissues and Central Nervous Physiology
  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

Rat soleus muscles were subjected to two types of overload with intent to induce fibre type transitions and modifications in muscular stiffness. The overloading techniques were respectively an endurance training program and a strength training program. The method of controlled releases was used to obtain tension-extension curves characterizing the elastic behaviour of the soleus. Fibre typing was made by myofibrillar ATPase staining and the effectiveness of the training programs was also evaluated by assessing enzymatic activities. Endurance training resulted in an increase of stiffness associated with a decrease of type II fibers. The opposite change was found as a result of strength training. These results demonstrate that endurance training and strength training induce opposite modifications in muscular stiffness which are correlated with fibre type transitions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bagby GJ, Sembrowich WL, Gollnick PD (1972) Myosin ATPase and fiber composition from trained and untrained rat skeletal muscle. Am J Physiol 223:1415–1417

    Google Scholar 

  • Baldwin KM, Winder WW, Terjung RL, Holloszy JO (1973) Glycolytic enzymes in different types of skeletal muscle: adaptation to exercise. Am J Physiol 225:962–966

    Google Scholar 

  • Bergmeyer HU, Bernt E (1974) Malate dehydrogenase. In: Bergmeyer HU (ed) Methoden der enzymatischen Analyse. Verlag-Chemie, Weinheim, pp 649–652

    Google Scholar 

  • Bergmeyer HU, Hillmann G, Schmidt E, Schmidt FW, Szasz G (1972) Empfehlungen der Deutschen Gesellschaft für klinisch experimentale Chemie. Begründung der optimalsten Standardbedingungen. Z Klin Chem U Klin Biochem 10:183–187

    Google Scholar 

  • Bergström J, Hultman E, Roch-Norlund AE (1972) Muscle glycogen synthetase in normal subjects. Scand J Clin Lab Invest 29:231–236

    Google Scholar 

  • Blangé T, Karemaker JM, Kramer AEJL (1972) Elasticity as an expression of cross-bridge activity in rat muscle. Pflügers Arch 336:277–288

    Google Scholar 

  • Bosco C, Tihanyi J, Komi PV, Fekete G, Apor P (1982) Store and recoil of elastic energy in slow and fast types of human skeletal muscles. Acta Physiol Scand 116:343–349

    Google Scholar 

  • Bressler BH, Clinch NF (1974) The compliance of contracting skeletal muscle. J Physiol (Lond) 237:477–493

    Google Scholar 

  • Brooke MH, Kaiser KK (1970) Muscle fiber types: how many and what kind? Arch Neurol 23:369–379

    Google Scholar 

  • Cavagna GA (1977) Storage and utilization of elastic energy in skeletal muscle. Exerc Sport Sci Rev 15:89–129

    Google Scholar 

  • Close RI (1972) Dynamic properties of mammalian skeletal muscles. Physiol Rev 52:129–197

    Google Scholar 

  • Exner GU, Staudte HW, Pette D (1973) Isometric training of rats. Effects upon fast and slow muscle and modification by an anabolic hormone (nandrolone decaonate). I. Female rats. Pflügers Arch 345:1–14

    Google Scholar 

  • Ford LE, Huxley AF, Simmons RM (1981) The relation between stiffness and filament overlap in stimulated frog muscle fibres. J Physiol (Lond) 311:219–249

    Google Scholar 

  • Goldspink G (1981) Design of muscle for locomotion and the maintenance of posture. Trends in Neurosciences 4:218–221

    Google Scholar 

  • Gonyea W, Bonde-Petersen F (1978) Alterations in muscle contractile properties and fiber composition after weight-lifting exercise in cats. Exp Neurol 50:75–84

    Google Scholar 

  • Goubel F (1978) Muscular compliance during isometric contraction. J Physiol (Paris) 74:609–614

    Google Scholar 

  • Green HJ, Reichmann H, Pette D (1983) Fibre type specific transformations in the enzyme activity pattern of rat vastus lateralis muscle by prolonged endurance training. Pflügers Arch 399:216–222

    Google Scholar 

  • Green HJ, Klug GA, Reichmann H, Seedorf U, Wieher W, Pette D (1984) Exercise-induced fibre type transitions with regard to myosin, parvalbumin, and sarcoplasmic reticulum in muscles of the rat. Pflügers Arch 400:432–438

    Google Scholar 

  • Gunderson H, Savage S, Rasmussen S, Wright K, Castro M (1985) Muscle enzymatic changes which occur with endurance and sprint training. Clin Physiol 5 (suppl 4):11

    Google Scholar 

  • Hill AV (1938) The heat of shortening and the dynamic constants of muscle. Proc R Soc Lond [Biol] 126:136–195

    Google Scholar 

  • Holloszy JO (1975) Adaptation of skeletal muscle to endurance exercise. Med Sci Sports Exerc 7:155–164

    Google Scholar 

  • Holloszy JO, Booth FW (1976) Biochemical adaptations to endurance exercise in muscle. Annu Rev Physiol 38:273–291

    Google Scholar 

  • Holloszy JO, Oscai LB, Don IJ, Molé PA (1970) Mitochondrial citric acid cycle and related enzymes: adaptative response to exercise. Biochem Biophys Res Commun 40:1368–1373

    Google Scholar 

  • Huxley AF, Simmons RM (1971) Proposed mechanism of force generation in striated muscle. Nature 233:533–538

    Google Scholar 

  • Jaweed MM, Herbison GJ, Ditunno JF (1977) Myosin ATPase activity after strengthening exercise. J Anat 214:371–381

    Google Scholar 

  • Kovanen V, Suominen H, Heikkinen E (1980) Connective tissue of “fast” and “slow” skeletal muscle — effects of endurance training. Acta Physiol Scand 108:173–180

    Google Scholar 

  • Kovanen V, Suominen H, Heikkinen E (1984) Mechanical properties of fast and slow skeletal muscle with special reference to collagen and endurance training. J Biochem 17:725–735

    Google Scholar 

  • Luginbuhl AJ, Dudley GA, Staron RS (1984) Fiber type changes in rat skeletal muscle after intense interval training. Histochemistry 81:55–58

    Google Scholar 

  • Molé PA, Baldwin KM, Terjung RL, Holloszy JO (1973) Enzymatic pathways of pyruvate metabolism in skeletal muscle: adaptations to exercise. Am J Physiol 224:50–54

    Google Scholar 

  • Morgan DL (1977) Separation of active and passive components of short-range stiffness of muscle. Am J Physiol 232:45–49

    Google Scholar 

  • Muller W (1974) Temporal progress of muscle adaptation to endurance training in hindlimb muscle of young rats. A histochemical and morphometrical study. Cell Tiss Res 156:61–88

    Google Scholar 

  • Parmley WW, Yeatman LA, Sonnenblick EH (1970) Differences between isotonic and isometric force-velocity relations in cardiac and skeletal muscle. Am J Physiol 219:546–550

    Google Scholar 

  • Pette D (1984) Activity-induced fast to slow transitions in mammalian muscle. Med Sci Sports Exerc 16:517–528

    Google Scholar 

  • Rack PMH, Westbury DR (1984) Elastic properties of the cat soleus tendon and their functional importance. J Physiol (Lond) 347:479–495

    Google Scholar 

  • Saltin B, Karlsson J (1971) Muscle glycogen utilization during work of different intensities. In: Pernon B, Saltin B (eds) Muscle metabolism during exercise. Plenum Press, New York, pp 289–300

    Google Scholar 

  • Sherwin AL, Karpati G, Bulcke JA (1969) Immunohistochemical localization of creatine phosphokinase in skeletal muscle. Proc Natl Acad Sci USA 64:171–175

    Google Scholar 

  • Sugi H (1979) The origin of the series elasticity in striated muscle fibers. In: Sugi H, Pollack GH (eds) Cross-bridge mechanism in muscle contraction. University Park Press, Baltimore, pp 85–102

    Google Scholar 

  • Szasz G, Gruber W, Bernt E (1976) Creatine kinase in serum. I. Determination of optimum reaction conditions. Clin Chem 22:650–656

    Google Scholar 

  • Tesch P (1980) Muscle fatigue in man with special reference to lactate accumulation during short term intense exercise. Acta Physiol Scand (Suppl) 480:1–40

    Google Scholar 

  • Walmsley B, Proske U (1981) Comparison of stiffness of soleus and medial gastrocnemius muscles in cats. J Neurophysiol 46:250–259

    Google Scholar 

  • Wells JB (1965) Comparison of mechanical properties between slow and fast mammalian muscles. J Physiol (Lond) 178:252–269

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Goubel, F., Marini, J.F. Fibre type transition and stiffness modification of soleus muscle of trained rats. Pflugers Arch. 410, 321–325 (1987). https://doi.org/10.1007/BF00580283

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00580283

Key words

Navigation