Summary
Physiological responses to repeated bouts of short duration maximal-intensity exercise were evaluated. Seven male subjects performed three exercise protocols, on separate days, with either 15 (S15), 30 (S30) or 40 (S40) m sprints repeated every 30 s. Plasma hypoxanthine (HX) and uric acid (UA), and blood lactate concentrations were evaluated pre- and postexercise. Oxygen uptake was measured immediately after the last sprint in each protocol. Sprint times were recorded to analyse changes in performance over the trials. Mean plasma concentrations of HX and UA increased during S30 and S40 (P<0.05), HX increasing from 2.9 (SEM 1.0) and 4.1 (SEM 0.9), to 25.4 (SEM 7.8) and 42.7 (SEM 7.5) µmol · l−1, and UA from 372.8 (SEM 19) and 382.8 (SEM 26), to 458.7 (SEM 40) and 534.6 (SEM 37) µmol · l−1, respectively. Postexercise blood lactate concentrations were higher than pretest values in all three protocols (P<0.05), increasing to 6.8 (SEM 1.5), 13.9 (SEM 1.7) and 16.8 (SEM 1.1) mmol · l−1 in S15, S30 and S40, respectively. There was no significant difference between oxygen uptake immediately after S30 [3.2 (SEM 0.1) l · min−1] and S40 [3.3 (SEM 0.4) l · min−1], but a lower value [2.6 (SEM 0.1) l · min−1] was found after S15 (P<0.05). The time of the last sprint [2.63 (SEM 0.04) s] in S15 was not significantly different from that of the first [2.62 (SEM 0.02) s]. However, in S30 and S40 sprint times increased from 4.46 (SEM 0.04) and 5.61 (SEM 0.07) s (first) to 4.66 (SEM 0.05) and 6.19 (SEM 0.09) s (last), respectively (P<0.05). These data showed that with a fixed 30-s intervening rest period, physiological and performance responses to repeated sprints were markedly influenced by sprint distance. While 15-m-sprints could be repeated every 30 s without decreases in performance, 40-m sprint times increased after the third sprint (P<0.05) and this exercise pattern was associated with a net loss to the adenine nucleotide pool.
Similar content being viewed by others
References
Åstrand I, Åstrand PO, Christensen EH, Hedman R (1960) Intermittent muscular work. Acta Physiol Scand 48:448–453
Bessman SP (1985) The creatine-creatine phosphate energy shuttle. Annu Rev Biochem 54:831–862
Boobis LH (1987) Metabolic aspects of fatigue during sprinting. In: Macleod D, Maughan RJ, Nimmo M, Reilly T, Williams C (eds) Exercise: benefits, limitations and adaptions. Spon, London, pp 116–140
Brooks S, Nevill ME, Meleagros L, Lakomy HKA, Hall GM, Bloom SR, Williams C (1990) The hormonal response to repetitive brief maximal exercise in humans. Eur J Appl Physiol 60:144–148
Cain DF, Davids RE (1962) Breakdown of adenosine triphosphate during a single contraction of working muscle. Biochem Biophys Res Commun 8:361–366
Christensen EH, Hedman R, Saltin B (1960) Intermittent and continuous running. Acta Physiol Scand 50:269–286
Essen B (1978) Studies on the regulation of metabolism in human skeletal muscle using intermittent exercise as an experimental model. Acta Physiol Scand [Suppl] 454:1–32
Harris RC, Sahlin K, Hultman E (1977) Phosphagen and lactate contents of m. quadriceps femoris of man after exercise. J Appl Physiol 43:852–857
Hellsten-Westing Y, Ekblom B, Sjödin B (1989) The metabolic relationship between hypoxanthine and uric acid in man following maximal short distance running. Acta Physiol Scand 137:341–345
Hellsten-Westing Y, Sollevi A, Sjödin B (1991) Plasma accumulation of hypoxanthine, uric acid and creatine kinase following exhausting runs of different durations in man. Eur J Appl Physiol 62:380–384
Holmyard DJ, Cheetham ME, Lakomy HKA, Williams C (1988) Effect of recovery duration on performance during multiple treadmill sprints. In: Reilly T, Lees A, Davids K, Murphy WJ (eds) Science and football. Spon, London, pp 134–142
Hultman E, Sjöholm H (1983) Substrate availability. In: Knuttgen HG, Vogel JA, Poortmans J (eds) Biochemistry of exercise. Human Kinetics, Champaign, Ill., pp 63–75
Ketai LH, Simon RH, Kreit JW, Grum CM (1987) Plasma hypoxanthine and exercise. Am Rev Respir Dis 136:98–101
Margaria R, Oliva RD, Di Prampero PE, Cerretelli P (1969) Energy utilization in intermittent exercise of supramaximal intensity. J Appl Physiol 26:752–756
Sahlin K, Broberg S (1990) Adenine nucleotide depletion in human muscle during exercise: causality and significance of AMP deamination. Int J Sports Med 11 [Suppl 2]:S62-S67
Saltin B, Essen B, Pedersen K (1976) Intermittent exercise: its physiology and some practical implications. In: Jokl E (ed) Medicine sport, vol 9. Advances in exercise physiology. Karger, Basel, pp 23–51
Sjödin B, Hellsten Westing Y, Apple F (1990) Biochemical mechanisms for oxygen free radical formation during exercise. Sports Med 10:236–254
Thorstensson A, Sjödin B, Karlsson J (1975) Enzyme activities and muscle strength after sprint training in man. Acta Physiol Scand 94:313–318
Wilkie D (1981) Shortage of chemical fuel as a cause of fatigue: studies by nuclear magnetic resonance and bicycle ergometry. In: Human muscle fatigue: physiological mechanisms. Ciba Foundation symposium 82. Pitman Medical, London, pp 102–119
Williams C (1990) Metabolic aspects of exercise. In: Reilly T, Sichir N, Snell P, Williams C (eds) Physiology of sports. Spon, London, pp 3–39
Wooton SA, Williams C (1983) The influence of recovery duration on repeated maximal sprints. In: Knuttgen HG, Vogel JA, Poortmans J (eds) Biochemistry of exercise. Human Kinetics, Champaign, Ill., pp 269–273
Wung WE, Howell SB (1980) Simultaneous liquid chromatography of 5-fluorouracil, uridine, hypoxanthine, xanthine, uric acid, allopurinol and oxipurinol in plasma. Clin Chem 26:1704–1708
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Balsom, P.D., Seger, J.Y., Sjödin, B. et al. Physiological responses to maximal intensity intermittent exercise. Europ. J. Appl. Physiol. 65, 144–149 (1992). https://doi.org/10.1007/BF00705072
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00705072