Skip to main content
Log in

The effects of a reduced exercise duration taper programme on performance and muscle enzymes of endurance cyclists

  • Published:
European Journal of Applied Physiology and Occupational Physiology Aims and scope Submit manuscript

Summary

The influence of tapering on the metabolic and performance parameters in endurance cyclists was investigated. Cyclists (n = 25) trained 5 days · week−1, 60 min·day−1, at 75–85% maximal oxygen consumption (VO2max) for 8 weeks and were then randomly assigned to a taper group: 4D (4 days;n = 7), 8D (8 days;n = 6), CON (control, 4 days rest;n = 6), NOTAPER (non-taper, continued training;n = 6). Muscle biopsy specimens taken before and after training and tapering were analysed for carnitine palmityltransferase (CPT), citrate synthase, ß-hydroxyacyl CoA dehydrogenase (HOAD), cytochrome oxidase (CYTOX), lactate dehydrogenase, glycogen and protein. Significant increases inVO2max (6%), a 60-min endurance cycle test (34.5%), oxidative enzymes (77–178%), glycogen (35%) and protein (34%) occurred following training. After the taper, HOAD and CPT decreased 25 % (P<0.05) and 26% respectively, in the CON. Post-taper CYTOX values were different (P<0.05) for 4D and 8D compared with CON. Muscle glycogen levels were increased (P<0.05) after tapering in the 4D, 8D and CON, but decreased in NOTAPER. Similarly, power output at ventilation threshold was significantly increased in the 4D (27.4 W) and 8D (27 W) groups, but decreased (22 W) in the NOTAPER. These findings suggest that tapering elicited a physiological adaptation by altering oxidative enzymes and muscle glycogen levels. Such an adaptation may influence endurance cycling during a laboratory performance test.

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.

Institutional subscriptions

Similar content being viewed by others

References

  • Banister EW, Calvert TW (1980) Planning for future performance: implications for long term training. Can J Appl Sport Sci 5:170–176

    PubMed  Google Scholar 

  • Bergmeyer HU (1974) Methods of enzymatic analysis, vol 2. Academic Press, New York

    Google Scholar 

  • Bergstrom J (1962) Muscle electrolytes in man. Scand J Clin Lab Invest 68:1–110

    Google Scholar 

  • Bergstrom J, Hermansen L, Hultman E, Saltin B (1967) Diet, muscle glycogen and physical performance. Acta Physiol Scand 71:140–150

    PubMed  Google Scholar 

  • Booth FW, Holloszy JO (1977) Cytochrome c turnover in rat skeletal muscles. J Biochem Chem 252:416–419

    Google Scholar 

  • Chance B, Williams GR (1955) Respiratory enzymes in oxidative phosphorylation: kinetics of oxygen utilization. J Biol Chem 7:383–393

    Google Scholar 

  • Chi MM, Hintz CS, Coyle EF, Martin WH, Ivy JL, Nemeth PM, Holloszy JO, Lowry OH (1983) Effects of detraining on enzymes of energy metabolism in individual human muscle fibers. Am J Physiol 244: C276-C287

    PubMed  Google Scholar 

  • Cohen J (1977) Statistical power analysis for the behavioral sciences. Academic Press, Orlando, Fla.

    Google Scholar 

  • Coulee RK (1987) Muscle glycogen and exercise endurance: a twenty-year perspective. Exerc Sport Sci Rev 15:1–29

    PubMed  Google Scholar 

  • Costill DL (1986) Inside running: basis of sport physiology. Benchmark Press, Indianapolis, pp 123–152

    Google Scholar 

  • Costill DL, Fink WJ, Getchell LH, Ivy JL, Witzmann FA (1979) Lipid metabolism in skeletal muscle of endurance-trained males and females. J Appl Physiol 47:787–791

    PubMed  Google Scholar 

  • Costill DL, King DS, Thomas R, Hargreaves M (1985) Effects of reduced training on muscular power in swimmers. Phys Sports Med 13:94–101

    Google Scholar 

  • Coyle EF, Martin WH, Sinacore DR, Joyner MJ, Hagberg JM, Holloszy JO (1984) Time course of loss of adaptations after stopping prolonged intense endurance training. J Appl Physiol 47:1857–1864

    Google Scholar 

  • Davies KJ, Packer L, Brooks GA (1981) Biochemical adaptation of mitochondria, muscle, and whole-animal respiration to endurance training. Arch Biochem Biophys 209:539–554

    PubMed  Google Scholar 

  • Dudley GA, Abraham WA, Terjung RJ (1982) Influence of exercise intensity and duration on biochemical adaptations in skeletal muscle. J Appl Physiol 53:844–850

    PubMed  Google Scholar 

  • Evans W, Pinney S, Young VR (1982) Suction applied to a muscle biopsy maximizes sample size. Med Sci Sports Exerc 14:101–103

    PubMed  Google Scholar 

  • Gollnick PD, Saltin B (1982) Significance of skeletal muscle oxidative enzyme enhancement with endurance training. Clin Physiol 2:1–12

    PubMed  Google Scholar 

  • Henriksson J, Reitman JS (1977) Time course of changes in human skeletal muscle succinate dehydrogenase and cytochrome oxidase activities and maximal uptake with physical activity and inactivity. Acta Physiol Scand 99:91–97

    PubMed  Google Scholar 

  • Hermansen L, Hultman E, Saltin B (1967) Muscle glycogen during prolonged severe exercise. Acta Physiol Scand 71:129–139

    PubMed  Google Scholar 

  • Hickson RC, Rosenkoetter MA (1981) Reduced training frequencies and maintenance of increased aerobic power. Med Sci Sports Exerc 13:13–16

    PubMed  Google Scholar 

  • Hinkle DE, Wiersma W, Jurs SG (1979) Applied statistics for the behavioral sciences. Houghton Mifflin, Boston, Mass.

    Google Scholar 

  • Holloszy JO (1976) Adaptations of muscular tissue to training. Proc Cardiovasc Dis 18:445–458

    Google Scholar 

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

    PubMed  Google Scholar 

  • Holloszy JO, Coyle EF (1984) Adaptations of skeletal muscle to endurance exercise and their metabolic consequences. J Appl Physiol 56:831–838

    PubMed  Google Scholar 

  • Houston ME, Bentzen H, Larsen H (1979) Interrelationships between skeletal muscle adaptations and performance as studied by detraining and retraining. Acta Physiol Scand 105:163–170

    PubMed  Google Scholar 

  • Hultman E (1967) Physiological role of muscle glycogen in man, with specific reference to exercise. Circ Res 20-21 [Suppl 1]:199–1114

    Google Scholar 

  • Hultman E, Bergstrom J, Roch-Norland AE (1971) Glycogen storage in human skeletal muscle. In: Pernow E, Saltin B (eds) Muscle metabolism during exercise. Plenum, New York, pp 273–288

    Google Scholar 

  • Jones NL, Ehrsam RE (1982) The anaerobic threshold. Exerc Sport Sci Rev 10:49–83

    PubMed  Google Scholar 

  • Lowry OH, Rosebrough NL Farr AL, Randall RJ (1951) Protein determination with the Folin phenol treagent. J Biol Chem 193:265–275

    PubMed  Google Scholar 

  • Lowry CV, Kimmey JS, Felder S, Chi MM, Kaiser KK, Passonneau PN, Kirk KA, Lowry OH (1978) Enzyme patterns in single human muscle fibers. J Biol Chem 253:8269–8277

    PubMed  Google Scholar 

  • McLellan TM, Skinner JS (1985) Submaximal endurance performance related to the ventilation thresholds. Can J Sport Sci 10:81–87

    Google Scholar 

  • Montpetit RR (1982) Etude de deux programmes d'affutage sur la performance en natation. In: Hogg J, Montpetit RR (eds) Tapering; Coaching the championship swimmer, Level III Technical. Canadian Amateur Swim Association, Ottawa, Ontario Neary JP,

    Google Scholar 

  • MacDougall JD, Bachus R, Wenger HA (1985) The relationship between the lactate and ventilatory thresholds: coincidental or cause and effect? Eur J Appl Physiol 54:104–108

    Google Scholar 

  • Neufer PD (1989) The effects of detraining and reduced training on the physiological adaptations of aerobic exercise training. Sports Med 8:302–321

    PubMed  Google Scholar 

  • Newsholme EA, Start C (1973) Regulation in metabolism. Wiley, London

    Google Scholar 

  • Peronnet F, Thibault G, Rhodes EC, McKenzie DC (1987) Correlation between ventilation threshold and endurance capability in marathon runners. Med Sci Sports Exerc 19:610–615

    PubMed  Google Scholar 

  • Pyke FS, Craig NP, Norton KI (1988) Physiological and psychological responses of pursuit and sprint track cyclists to a period of reduced training. In: Burke ER, Newsom MM (eds) Medical and scientific aspects of cycling. Human Kinetics, Champaign, Ill

    Google Scholar 

  • Schantz PG (1986) Plasticity of human skeletal muscle. Acta Physiol Scand [Suppl] 558:6–62

    Google Scholar 

  • Sharp DS, Gahlinger PM (1988) Regression analysis in biological research: sample size and statistical power. Med Sci Sports Exerc 20:605–610

    PubMed  Google Scholar 

  • Soussi B, Idstrom JP, Schersten T, Byland-Fellenius AC (1989) Kinetic parameters of cytochrome c oxidase in rat skeletal muscle: effect of endurance training. Acta Physiol Scand 135:373–379

    PubMed  Google Scholar 

  • Suarez RK, Brown GS, Hochachka PW (1986) Metabolic sources of energy for hummingbird flight. Am J Physiol 251:R537-R542

    PubMed  Google Scholar 

  • Thoden JS (1991) Testing aerobic power. In: MacDougall JD, Wenger HA, Green HJ (eds) Physiological testing of the highperformance athlete. Human Kinetics, Champaign, Ill

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Neary, J.P., Martin, T.P., Reid, D.C. et al. The effects of a reduced exercise duration taper programme on performance and muscle enzymes of endurance cyclists. Europ. J. Appl. Physiol. 65, 30–36 (1992). https://doi.org/10.1007/BF01466271

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01466271

Key words

Navigation