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Effect of Passive and Active Recovery on PCr Kinetics

  • Takayoshi Yoshida
  • Hiroshi Watari
Chapter
  • 181 Downloads

Abstract

Recently, 31phosphorus-nuclear magnetic resonance spectroscopy (31P-MRS) has been used as a noninvasive technique to measure changes in the concentrations of adenosine 5’-triphosphate (ATP), phosphocreatine (PCr) and inorganic phosphate (Pi), as well as the intramuscular pH, both during and after exercise. Splitting of the Pi peak into two has been observed during exercise and is attributable to two different pH distributions in exercising muscle (high pH and low pH) (1, 3, 5, 8, 11, 15). Previously, we reported that the two split Pi peaks showed different time courses at the onset of exercise and during recovery (16, 19, 22); high-pH Pi increased promptly at the onset of exercise and disappeared rapidly after exercise, while the low-pH Pi peak increased gradually after a delay of approximately 60 sec at the onset of exercise and decreased over a longer period after exercise was stopped.

Keywords

Active Recovery Recovery Test Passive Recovery Repeated Exercise Glycolytic Fiber 
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References

  1. 1.
    Achten E., M. Van Cauteren, R. Willem, R. Luypaert, WJ. Malaisse, G. Van Bosch, G. Delanghe, K. De Meirleir, and M. Osteaux. 31P-NMR spectroscopy and the metabolic properties of different muscle fibers. J. Appl. Physiol. 68: 644–649, 1990.PubMedGoogle Scholar
  2. 2.
    Chance, B., J.S. Leigh Jr, J. Kent, and K. McCully. Metabolic control principles and 31P-NMR. Fed. Proc. 45:2915–2920,1986.PubMedGoogle Scholar
  3. 3.
    Clark III, B.J., M.A. Acker, K.K. McCully, H.V Subramanian, R.L. Hammond, S. Salmons, B. Chance, and L.W. Stephenson. In vivo 31P-NMR spectroscopy of chronically stimulated canine skeletal muscle. Am. J. Physiol 254 (Cell Physiol. 23): C258–C266, 1988.PubMedGoogle Scholar
  4. 4.
    Hermansen, L., and I. Stensvold. Production and removal of lactate during exercise in man. Acta Physiol. Scand. 86: 191–201, 1972.PubMedCrossRefGoogle Scholar
  5. 5.
    Jeneson, J.A.L., M.W. Wesseling, R.W. De Boer, and H.G. Amelink. Peak-splitting of inorganic phosphate during exercise, anatomy or physiology? A MRI-guided 31P MRS study of human forearm muscle. In: Proceedings of the Eighth Annual Meeting of Society of Magnetic Resonance in Medicine. Abstract 1030. Society of Magnetic Resonance in Medicine, Berkeley, California, 1989.Google Scholar
  6. 6.
    Kushmerick, M.J., and R.A. Meyer. Chemical changes in rat leg muscle by phosphorus nuclear magnetic resonance. Am. J. Physiol. 248 (Cell Physiol. 17): C542–C549, 1985.PubMedGoogle Scholar
  7. 7.
    McLellan, T.M., and J.S. Skinner. Blood lactate removal during active recovery related to the aerobic threshold. Int. J. Sports Med. 3: 224–229, 1982.CrossRefGoogle Scholar
  8. 8.
    Meyer, R.A., T.R. Brown, and M.J. Kushmerick. Phosphorus nuclear magnetic resonance of fast-and slowtwitch muscle. Am. J. Physiol. 248 (Cell Physiol. 17): C279–C287, 1985.PubMedGoogle Scholar
  9. 9.
    Mizuno, M., L.O. Justesen, J. Bedolla, D.B. Riedman, N.H. Secher, and B. Quistroff. Partial curarization abolishes splitting of the inorganic phosphate peak in P-NMR spectroscopy during intense forearm exercise in man. Acta Physiol Scand. 139: 611–612, 1990.PubMedCrossRefGoogle Scholar
  10. 10.
    Mole, P.A., R.L. Coulson, J.R. Caton, B.G, Nichols, and T.J. Barstow. In vivo 31P-NMR in human muscle: transient patterns with exercise. J. Appl Physiol. 59: 101–104, 1985.PubMedGoogle Scholar
  11. 11.
    Park, J.H., R.L. Brown, C.R. Park, K.K. McCully, M. Cohn, J. Hasellgrove, and B. Chance. Functional pools of oxidative and glycolytic fibers in human muscle observed by 31P magnetic resonance spectroscopy during exercise. Proc. Natl Acad. Sci. USA 84: 8976–8980, 1987.PubMedCrossRefGoogle Scholar
  12. 12.
    Quistorff, B., L. Johansen, and K. Sahlin. Absence of phosphocreatine resynthesis in human calf muscle during ischemic recovery. cBiochem. J. 291: 681–686, 1992.Google Scholar
  13. 13.
    Saltin, B., and P.D. Gollnick. Skeletal muscle adaptability: significance for metabolism and performance. In: Handbook of physiology. Skeletal Muscle. Bethesda, MD: Am. Physiol. Soc, 1983, Sect. 10, Chapt.19, p.555–631.Google Scholar
  14. 14.
    Tesch, P.A., A Thorsson, and N. Fujitsuka. Creatine phosphate in fiber types of skeletal muscle before and after exhaustive exercise. J. Appl Physiol. 66: 1756–1759, 1989.PubMedGoogle Scholar
  15. 15.
    Vandenborne, K., K. McCully, H. Kakihara, M. Prammer, L. Bolinger, J.A. Detre, K. De Meirleie, K. Walter, and B. Chance. Metabolic heterogeneity in human calf muscle during maximal exercise. Proc. Natl. Acad. Sci. USA, 88: 5714–5718, 1991.PubMedCrossRefGoogle Scholar
  16. 16.
    Yoshida, T., and H. Watari. Noninvasive and continuous determination of energy metabolism during muscular contraction and recovery. Med. Sci. Sport Exerc. 37: 364–373, 1992.Google Scholar
  17. 17.
    Yoshida, T., and H. Watari. Muscle metabolism during repeated exercise studied by 31P-MRS. Ann. Physiol Anthrop. 11: 241–250, 1992.CrossRefGoogle Scholar
  18. 18.
    Yoshida, T., and H. Watari. Effect of hypoxia on muscle metabolite during exercise studied by 31P-MRS. Med. Sci. Sport Exerc. 25(Suppl): S174, 1993.CrossRefGoogle Scholar
  19. 19.
    Yoshida, T., and H. Watari. 31P-MRS study of the time course of energy metabolism during exercise and recovery. Eur. J. Appl. Physiol. 66: 494–499, 1993.CrossRefGoogle Scholar
  20. 20.
    Yoshida, T., and H. Watari. Metabolic consequences of repeated exercise in long distance runners. Eur. J. Appl Physiol. 67: 261–265, 1993.CrossRefGoogle Scholar
  21. 21.
    Yoshida, T., and H. Watari. Changes in intracellular pH during repeated exercise. Eur. J. Appl Physiol. 67: 274–278, 1993.CrossRefGoogle Scholar
  22. 22.
    Yoshida, T., and H. Watari. Exercise-induced splitting of the inorganic phosphate peak: investigation by time-resolved 31 P-nuctear magnetic resonance spectroscopy. Eur. J. Appl Physiol. 69: 465–73, 1994.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 1996

Authors and Affiliations

  • Takayoshi Yoshida
    • 1
  • Hiroshi Watari
    • 1
  1. 1.Exercise Physiology LaboratoryFaculty of Health and Sports Sciences Osaka UniversityToyonakaJapan

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