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Sports Medicine
Erschienen in: Sports Medicine 9/2005

01.09.2005 | Review Article

Multiple Sprint Work

Physiological Responses, Mechanisms of Fatigue and the Influence of Aerobic Fitness

verfasst von: Dr Mark Glaister

Erschienen in: Sports Medicine | Ausgabe 9/2005

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Abstract

The activity patterns of many sports (e.g. badminton, basketball, soccer and squash) are intermittent in nature, consisting of repeated bouts of brief (≤-second) maximal/near-maximal work interspersed with relatively short (≤60-second) moderate/low-intensity recovery periods. Although this is a general description of the complex activity patterns experienced in such events, it currently provides the best means of directly assessing the physiological response to this type of exercise. During a single short (5- to 6-second) sprint, adenosine triphosphate (ATP) is resynthesised predominantly from anaerobic sources (phosphocreatine [PCr] degradation and glycolysis), with a small (<10%) contribution from aerobic metabolism. During recovery, oxygen uptake (V̇O2) remains elevated to restore homeostasis via processes such as the replenishment of tissue oxygen stores, the resynthesis of PCr, the metabolism of lactate, and the removal of accumulated intracellular inorganic phosphate (Pi). If recovery periods are relatively short, V̇O2 remains elevated prior to subsequent sprints and the aerobic contribution to ATP resynthesis increases. However, if the duration of the recovery periods is insufficient to restore the metabolic environment to resting conditions, performance during successive work bouts may be compromised. Although the precise mechanisms of fatigue during multiple sprint work are difficult to elucidate, evidence points to a lack of available PCr and an accumulation of intracellular Pi as the most likely causes. Moreover, the fact that both PCr resynthesis and the removal of accumulated intracellular Pi are oxygen-dependent processes has led several authors to propose a link between aerobic fitness and fatigue during multiple sprint work. However, whilst the theoretical basis for such a relationship is compelling, corroborative research is far from substantive. Despite years of investigation, limitations in analytical techniques combined with methodological differences between studies have left many issues regarding the physiological response to multiple sprint work unresolved. As such, multiple sprint work provides a rich area for future applied sports science research.
Literatur
1.
Bangsbo J, Nørregaard L, Thorsø F. Activity profile of competition soccer. Can J Sports Sci 1991; 16 (2): 110–6
2.
3.
Docherty D, Wenger HA, Neary P. Time-motion analysis related to the physiological demands of rugby. J Hum Mov Stud 1988; 14 (6): 269–77
4.
5.
Reilly T, Thomas V. A motion analysis of work-rate in different positional roles in professional football match-play. J Hum Mov Stud 1976; 2: 87–97
6.
Withers RT, Maricic Z, Wasilewski S, et al. Match analyses of Australian professional soccer players. J Hum Mov Stud 1982; 8: 159–76
7.
8.
Mayhew SR, Wenger HA. Time-motion analysis of professional soccer. J Hum Mov Stud 1985; 11 (1): 49–52
9.
Brodowicz GR, Schatz JC, Svoboda MD. Frequency, intensity and duration of locomotion of semi-professional soccer players. J Hum Mov Stud 1990; 18: 63–71
10.
Bangsbo J. The physiology of soccer: with special reference to intense intermittent exercise. Acta Physiol Scand Suppl 1994; 619: 1–155PubMed
11.
Nicholas CW. Anthropometric and physiological characteristics of rugby union football players. Sports Med 1997; 23 (6): 375–96PubMedCrossRef
12.
Reilly T. Energetics of high-intensity exercise (soccer) with particular reference to fatigue. J Sports Sci 1997; 15 (3): 257–63PubMedCrossRef
13.
Christmass MA, Richmond SE, Cable NT, et al. Exercise intensity and metabolic response in singles tennis. J Sports Sci 1998; 16: 739–47PubMedCrossRef
14.
Docherty D. A comparison of heart rate responses in racquet games. Br J Sports Med 1982; 16 (2): 96–100PubMedCrossRef
15.
Elliott B, Dawson B, Pyke F. The energetics of singles tennis. J Hum Mov Stud 1985; 11: 11–20
16.
Faccini P, Dal Monte A. Physiologic demands of badminton match play. Am J Sports Med 1996; 24 (6): S64–6
17.
Liddle SD, Murphy MH, Bleakley W. A comparison of the physiological demands of singles and doubles badminton: a heart rate and time-motion analysis. J Hum Mov Stud 1996; 30: 159–76
18.
Majumdar P, Khanna GL, Malik V, et al. Physiological analysis to quantify training load in badminton. Br J Sports Med 1997; 31: 342–5PubMedCrossRef
19.
20.
Fox EL. Sports physiology. Philadelphia (PA): Saunders, 1984
21.
Maud PJ. Physiological and anthropometric parameters that describe a rugby union team. Br J Sports Med 1983; 17: 16–23PubMedCrossRef
22.
Seliger V, Ejam M, Pauer M, et al. Energy metabolism in tennis. Int Z Angew Physiol 1973; 31: 333–40PubMed
23.
Boyle PM, Mahoney CA, Wallace WFM. The competitive demands of elite male field hockey. J Sport Med Phys Fit 1994; 34: 235–41
24.
Ballor DL, Volovsek AJ. Effect of exercise to rest ratio on plasma lactate concentration at work rates above and below maximum oxygen uptake. Eur J Appl Physiol 1992; 65: 365–9CrossRef
25.
Bergeron MF, Maresh CM, Kraemer WJ, et al. Tennis: a physiological profile during match play. Int J Sports Med 1991; 12 (5): 474–9PubMedCrossRef
26.
Balsom PD. High intensity intermittent exercise: performance and metabolic responses with very high intensity short duration work periods [dissertation]. Stockholm: Karolinska Institute, 1995
27.
Brooks S, Nevill ME, Meleagros L, et al. The hormonal responses to repetitive brief maximal exercise in humans. Eur J Appl Physiol 1990; 60 (2): 144–8CrossRef
28.
Christmass MA, Dawson B, Passeretto P, et al. A comparison of skeletal muscle oxygenation and fuel use in sustained continuous and intermittent exercise. Eur J Appl Physiol 1999; 80: 423–35CrossRef
29.
Gaitanos GC, Williams C, Boobis LH, et al. Human muscle metabolism during intermittent maximal exercise. J Appl Physiol 1993; 75 (2): 712–9PubMed
30.
Hamilton AL, Nevill ME, Brooks S, et al. Physiological responses to maximal intermittent exercise: differences between endurance-trained runners and games players. J Sports Sci 1991; 9 (4): 371–82PubMedCrossRef
31.
Holmyard DJ, Cheetham ME, Lakomy HKA, et al. Effect of recovery duration on performance during multiple treadmill sprints. In: Reilly T, Lees A, Davids K, et al. editors. Science and football. London: F & N Spon, 1988: 134–42
32.
Bogdanis GC, Nevill ME, Lakomy HKA, et al. Power output and muscle metabolism during and following recovery from 10 and 20 s of maximal sprint exercise in humans. Acta Physiol Scand 1998; 163: 261–72PubMedCrossRef
33.
Parolin ML, Chesley A, Matsos MP, et al. Regulation of skeletal muscle glycogen phosphorylase and PDH during maximal intermittent exercise. Am J Physiol 1999; 277: E890–900
34.
Bangsbo J, Krustrup P, González-Alonso J, et al. ATP production and efficiency of human skeletal muscle during intense exercise: effect of previous exercise. Am J Physiol 2001; 280 (6): E956–64
35.
Hultman E, Sjöholm H. Energy metabolism and contraction force of human skeletal muscle in situ during electrical stimulation. J Physiol 1983; 345: 525–32PubMed
36.
Walter G, Vandenborne K, McCully KK, et al. Noninvasive measurement of phosphocreatine recovery kinetics in single human muscles. Am J Physiol 1997; 272: C525–34
37.
Hultman E, Bergström M, Spriet LL, et al. Energy metabolism and fatigue. In: Taylor A, Gollnick P, Green H, et al. editors. Biochemistry of sport and exercise VII. Champaign (IL): Human Kinetics, 1990: 73–92
38.
Jones NL, McCartney N, Graham T, et al. Muscle performance and metabolism in maximal isokinetic cycling at slow and fast speeds. J Appl Physiol 1985; 59 (1): 132–6PubMed
39.
Gastin PB. Energy system interaction and relative contribution during maximal exercise. Sports Med 2001; 31 (10): 725–41PubMedCrossRef
40.
Greenhaff PL, Bodin K, Casey A, et al. Dietary creatine supplementation and fatigue during high-intensity exercise in humans. In: Maughan RJ, Shirreffs SM, editors. Biochemistry of sport and exercise IX. Champaign (IL): Human Kinetics, 1996: 219–42
41.
Bangsbo J, Graham T, Johansen L, et al. Elevated muscle acidity and energy production during exhaustive exercise in humans. Am J Physiol 1992; 263: R891–9
42.
Hellsten-Westing Y, Norman B, Balsom PD, et al. Decreased resting levels of adenine nucleotides in human skeletal muscle after high-intensity training. J Appl Physiol 1993; 74 (5): 2523–8PubMed
43.
Astrand I, Astrand PO, Christensen EH, et al. Myohemoglobin as an oxygen-store in man. Acta Physiol Scand 1960; 48: 454–60PubMedCrossRef
44.
Christensen EH, Hedman R, Saltin B. Intermittent and continuous running. Acta Physiol Scand 1960; 50: 269–86PubMedCrossRef
45.
Margaria R, Oliva RD, Di Prampero PE, et al. Energy utilisation in intermittent exercise of supramaximal intensity. J Appl Physiol 1969; 26 (6): 752–6PubMed
46.
Boobis L, Williams C, Wootton SA. Human muscle metabolism during brief maximal exercise. J Physiol 1982; 338: 21P-2P
47.
McMahon S, Jenkins D. Factors affecting the rate of phosphocreatine resynthesis following intense exercise. Sports Med 2002; 32 (12): 761–84PubMedCrossRef
48.
Blei ML, Conley KE, Kushmerick MJ. Separate measures of ATP utilization and recovery in human skeletal muscle. J Physiol 1993; 465: 203–22PubMed
49.
Bogdanis GC, Nevill ME, Boobis LH, et al. Recovery of power output and muscle metabolites following 30 s of maximal sprint cycling in man. J Physiol 1995; 482 (2): 467–80PubMed
50.
Cooke SR, Petersen SR, Quinney HA. The influence of maximal aerobic power on recovery of skeletal muscle following anaerobic exercise. Eur J Appl Physiol 1997; 75 (6): 512–9CrossRef
51.
Harris RC, Edwards RHT, Hultman E, et al. The time course of phosphorylcreatine resynthesis during recovery of the quadriceps muscle in man. Pflugers Arch 1976; 367: 137–42PubMedCrossRef
52.
Haseler LJ, Hogan MC, Richardson RS. Skeletal muscle phosphocreatine recovery in exercise-trained humans is dependent on O2 availability. J Appl Physiol 1999; 86 (6): 2013–8PubMed
53.
Quistorff B, Johansen L, Sahlin K. Absence of phosphocreatine resynthesis in human calf muscle during ischaemic recovery. Biochem J 1992; 291: 681–6
54.
Roussel M, Bendahan D, Mattei JP, et al. 31P magnetic resonance spectroscopy study of phosphocreatine recovery kinetics in skeletal muscle: the issue of intersubject variability. Biochim Biophys Acta 2000; 1457: 18–26PubMedCrossRef
55.
Sahlin K, Harris RC, Hultman E. Resynthesis of creatine phosphate in human muscle after exercise in relation to intramuscular pH and availability of oxygen. Scand J Clin Lab Invest 1979; 39: 551–8PubMedCrossRef
56.
Takahashi H, Inaki M, Fujimoto K, et al. Control of the rate of phosphocreatine resynthesis after exercise in trained and untrained human quadriceps muscles. Eur J Appl Physiol 1995; 71 (5): 396–404CrossRef
57.
Thompson CH, Kemp GJ, Sanderson AL, et al. Skeletal muscle mitochondrial function studied by kinetic analysis of postexercise phosphocreatine resynthesis. J Appl Physiol 1995; 78 (6): 2131–9PubMed
58.
Idström JP, Subramanian VH, Chance B, et al. Oxygen dependence of energy metabolism in contracting and recovering rat skeletal muscle. Am J Physiol 1985; 248 (17): H40–8
59.
Bergström M, Hultman E. Relaxation and force during fatigue and recovery of the human quadriceps muscle: relations to metabolite changes. Pflugers Arch 1991; 418: 153–60PubMedCrossRef
60.
Metzger JM, Fitts RH. Role of intracellular pH in muscle fatigue. J Appl Physiol 1987; 62 (4): 1392–7PubMed
61.
62.
Sahlin K, Gorski J, Edström L. Influence of ATP turnover and metabolite changes on IMP formation and glycolysis in rat skeletal muscle. Am J Physiol 1990; 259: C409–12
63.
Taylor DJ, Bore PJ, Styles P, et al. Bioenergetics of intact human muscle: a 31P nuclear magnetic resonance study. Mol Biol Med 1983; 1 (1): 77–94PubMed
64.
Sahlin K, Harris RC, Nylind B, et al. Lactate content and pH in muscle samples obtained after dynamic exercise. Pflugers Arch 1976; 367: 143–9PubMedCrossRef
65.
Bangsbo J. Regulation of muscle glycogenolysis and glycolysis during intense exercise: in vivo studies using repeated intense exercise. In: Maughan RJ, Shirreffs SM, editors. Biochemistry of exercise IX. Champaign (IL): Human Kinetics, 1996: 261–75
66.
Putman CT, Jones NL, Lands LC, et al. Skeletal muscle pyruvate dehydrogenase activity during maximal exercise in humans. Am J Physiol 1995; 269: E458–68
67.
Balsom PD, Gaitanos GC, Söderlund K, et al. High-intensity exercise and muscle glycogen availability in humans. Acta Physiol Scand 1999; 165: 337–45PubMedCrossRef
68.
Asmussen E, Klausen K, Nielsen LE, et al. Lactate production and anaerobic work capacity after prolonged exercise. Acta Physiol Scand 1974; 90: 731–42PubMedCrossRef
69.
Greenhaff PL, Gleeson M, Maughan RJ. The effects of a glycogen loading regimen on acid-base status and blood lactate concentration before and after a fixed period of high-intensity exercise in man. Eur J Appl Physiol 1988; 57: 254–9CrossRef
70.
Maughan RJ, Poole DC. The effects of a glycogen-loading regimen on the capacity to perform anaerobic exercise. Eur J Appl Physiol 1981; 46: 211–9CrossRef
71.
Bangsbo J, Graham T, Kiens B, et al. Elevated muscle glycogen and anaerobic energy production during exhaustive exercise in man. J Physiol 1992; 451: 205–27PubMed
72.
Jacobs I. Lactate concentrations after short, maximal exercise at various glycogen levels. Acta Physiol Scand 1981; 111: 465–9PubMedCrossRef
73.
Ren JM, Broberg S, Sahlin K, et al. Influence of reduced glycogen level on glycogenolysis during short-term stimulation in man. Acta Physiol Scand 1990; 139: 467–74PubMedCrossRef
74.
Spencer MK, Katz A. Role of glycogen in control of glycolysis and IMP formation in human muscle during exercise. Am J Physiol 1991; 260: E859–64
75.
Symons JD, Jacobs I. High-intensity exercise performance is not impaired by low intramuscular glycogen. Med Sci Sports Exerc 1989; 21 (5): 550–7PubMed
76.
Boscá L, Aragón JJ, Sols A. Modulation of muscle phosphofructokinase at physiological concentration of enzyme. J Biol Chem 1985; 260 (4): 2100–7PubMed
77.
Dobson GP, Yamamoto E, Hochachka PW. Phosphofructokinase control in muscle: nature and reversal of pH-dependent ATP inhibition. Am J Physiol 1986; 250: R71–6
78.
Spriet LL, Söderlund K, Bergström M, et al. Skeletal muscle glycogenolysis, glycolysis, and pH during electrical stimulation in men. J Appl Physiol 1987; 62 (2): 616–21PubMed
79.
Parmeggiani A, Bowman RH. Regulation of phosphofructokinase activity by citrate in normal and diabetic muscle. Biochem Biophys Res Commun 1963; 12 (4): 268–73PubMedCrossRef
80.
Passonneau JV, Lowry OH. P-fructokinase and the control of the citric acid cycle. Biochem Biophys Res Commun 1963; 13 (5): 372–9CrossRef
81.
Taylor WM, Halperin ML. Regulation of pyruvate dehydrogenase in muscle. J Biol Chem 1973; 248 (17): 6080–3PubMed
82.
Wu TFL, Davis EJ. Regulation of glycolytic flux in an energetically controlled cell-free system: the effects of adenine nucleotide ratios, inorganic phosphate, pH, and citrate. Arch Biochem Biophys 1981; 209 (1): 85–99PubMedCrossRef
83.
Peters SJ, Spriet LL. Skeletal muscle phosphofructokinase activity examined under physiological conditions in vitro. J Appl Physiol 1995; 78 (5): 1853–8PubMed
84.
Conley KE, Ordway GA, Richardson RS. Deciphering the mysteries of myoglobin in striated muscle. Acta Physiol Scand 2000; 168: 623–34PubMedCrossRef
85.
Richardson RS, Newcomer SC, Nnoyszewski EA. Skeletal muscle intracellular PO2 assessed by myoglobin desaturation: response to graded exercise. J Appl Physiol 2001; 91 (6): 2679–85PubMed
86.
Wittenberg BA, Wittenberg JB, Caldwell PRB. Role of myoglobin in the oxygen supply to red skeletal muscle. J Biol Chem 1975; 250 (23): 9038–43PubMed
87.
Bangsbo J, Krustrup P, González-Alonso J, et al. Muscle oxygen kinetics at onset of intense dynamic exercise in humans. Am J Physiol 2000; 279: R899–906
88.
Akeson A, Biörck G, Simon R. On the content of myoglobin in human muscles. Acta Med Scand 1968; 183: 307–16PubMedCrossRef
89.
Harris RC, Hultman E, Kaijser L, et al. The effect of circulatory occlusion on isometric exercise capacity and energy metabolism of the quadriceps muscle in man. Scand J Clin Lab Invest 1975; 35 (1): 87–95PubMedCrossRef
90.
Molé PA, Chung Y, Tran TK, et al. Myoglobin desaturation with exercise intensity in human gastrocnemius muscle. Am J Physiol 1999; 277: R173–80
91.
Richardson RS, Noyszewski EA, Kendrick KF, et al. Myoglobin O2 desaturation during exercise. J Clin Invest 1995; 96 (4): 1916–26PubMedCrossRef
92.
Bogdanis GC, Nevill ME, Boobis LH, et al. Contribution of phosphocreatine and aerobic metabolism to energy supply during repeated sprint exercise. J Appl Physiol 1996; 80 (3): 876–84PubMed
93.
Trump ME, Heigenhauser GJF, Putman CT, et al. Importance of muscle phosphocreatine during intermittent maximal cycling. J Appl Physiol 1996; 80 (5): 1574–80PubMed
94.
Bahr R, Grønnerød O, Sejersted OM. Effect of supramaximal exercise on excess postexercise O2 consumption. Med Sci Sports Exerc 1992; 24 (1): 66–71PubMed
95.
Bangsbo J, Hellsten Y. Muscle blood flow and oxygen uptake in recovery from exercise. Acta Physiol Scand 1998; 162: 305–12PubMedCrossRef
96.
Børsheim E, Knardahl S, Høstmark AT, et al. Adrenergic control of post-exercise metabolism. Acta Physiol Scand 1998; 162: 313–23PubMedCrossRef
97.
Gaesser GA, Brooks GA. Metabolic bases of excess post-exercise oxygen consumption: a review. Med Sci Sports Exerc 1984; 16 (1): 29–43PubMed
98.
Bohnert B, Ward SA, Whipp BJ. Effects of prior arm exercise on pulmonary gas exchange kinetics during high-intensity leg exercise in humans. Exp Physiol 1998; 83: 557–70PubMed
99.
Gausche MA, Harmon T, Lamarra N, et al. Pulmonary O2 uptake kinetics in humans are speeded by a bout of prior exercise above, but not below, the lactate threshold [abstract]. J Physiol 1989; 417: 138P
100.
Gerbino A, Ward SA, Whipp BJ. Effects of prior exercise on pulmonary gas-exchange kinetics during high-intensity exercise in humans. J Appl Physiol 1996; 80 (1): 99–107PubMed
101.
Rossiter HB, Ward SA, Kowalchuk JM, et al. Effects of prior exercise on oxygen uptake and phosphocreatine kinetics during high-intensity knee-extension exercise in humans. J Physiol 2001; 537 (1): 291–303PubMedCrossRef
102.
Jones AM, Koppo K, Burnley M. Effects of prior exercise on metabolic and gas exchange responses to exercise. Sports Med 2003; 33 (13): 949–71PubMedCrossRef
103.
Grassi B, Poole DC, Richardson RS, et al. Muscle O2 uptake kinetics in humans: implications for metabolic control. J Appl Physiol 1996; 80 (3): 988–98PubMed
104.
McCully KK, Authier B, Olive J, et al. Muscle fatigue: the role of metabolism. Can J Appl Physiol 2002; 27 (1): 70–82PubMedCrossRef
105.
Balsom PD, Seger JY, Sjödin B, et al. Maximal-intensity intermittent exercise: effect of recovery duration. Int J Sports Med 1992; 13 (7): 528–33PubMedCrossRef
106.
Wootton S, Williams C. The influence of recovery duration on repeated maximal sprints. In: Knuttgen HG, Vogel JA, Poortmans J, editors. Biochemistry of exercise, international series in sports science, vol. XIII. Champaign (IL): Human Kinetics, 1983: 269–73
107.
Robinson JM, Stone MH, Johnson RL, et al. Effects of different weight training exercise/rest intervals on strength, power and high intensity exercise endurance. J Strength Cond Res 1995; 9 (4): 216–21
108.
Stone MH, Sanborn K, Smith LL, et al. Effects of in-season (5 weeks) creatine and pyruvate supplementation on anaerobic performance and body composition in American football players. Int J Sport Nutr 1999; 9 (2): 146–65PubMed
109.
Abbate F, Sargeant AJ, Verdijk PW, et al. Effects of high-frequency initial pulses and posttetanic potentiation on power output of skeletal muscle. J Appl Physiol 2000; 88 (1): 35–40PubMed
110.
Güllich A, Schmidtbleicher D. MVC-induced short-term potentiation of explosive force. N Stud Athletics 1996; 11 (4): 67–81
111.
112.
Smith JC, Fry AC, Weiss LW, et al. The effects of high-intensity exercise on a 10-second sprint cycle test. J Strength Cond Res 2001; 15 (3): 344–8PubMed
113.
Bigland-Ritchie B, Woods J. Changes in muscle contractile properties and neural control during human muscular fatigue. Muscle Nerve 1984; 7 (9): 691–9PubMedCrossRef
114.
Cherry PW, Lakomy HKA, Boobis LH, et al. Rapid recovery of power output in females. Acta Physiol Scand 1998; 164: 79–87PubMedCrossRef
115.
Duchateau J, Hainaut K. Electrical and mechanical failures during sustained and intermittent contractions in humans. J Appl Physiol 1985; 58 (3): 942–7PubMed
116.
Balsom PD, Seger JY, Sjödin B, et al. Physiological responses to maximal intensity intermittent exercise. Eur J Appl Physiol 1992; 65: 144–9CrossRef
117.
Hitchcock HC. Recovery of short-term power after dynamic exercise. J Appl Physiol 1989; 67 (2): 677–81PubMed
118.
Holmyard DJ, Nevill ME, Lakomy HKA, et al. Recovery of power output after maximal treadmill sprinting [abstract]. J Sports Sci 1994; 12 (2): 140
119.
Sahlin K, Ren JM. Relationship of contraction capacity to metabolic changes during recovery from a fatiguing contraction. J Appl Physiol 1989; 67 (2): 648–54PubMed
120.
Sargeant AJ, Dolan P. Effect of prior exercise on maximal short-term power output in humans. J Appl Physiol 1987; 63 (4): 1475–80PubMed
121.
Aaserud R, Gramvik P, Olsen SR, et al. Creatine supplementation delays onset of fatigue during repeated bouts of sprint running. Scand J Med Sci Sports 1998; 8 (5): 247–51PubMedCrossRef
122.
Balsom PD, Ekblom B, Söderlund K, et al. Creatine supplementation and dynamic high-intensity intermittent exercise. Scand J Med Sci Sports 1993; 3: 143–9CrossRef
123.
Bogdanis GC, Nevill ME, Lakomy HKA, et al. The effects of oral creatine supplementation on power output during repeated treadmill sprinting. J Sports Sci 1996; 14: 65–6
124.
Jones AM, Atter T, Georg KP. Oral creatine supplementation improves multiple sprint performance in elite ice-hockey players. J Sport Med Phys Fitness 1999; 39 (3): 189–96
125.
Mujika I, Padilla S, Ibanéz J, et al. Creatine supplementation and sprint performance in soccer players. Med Sci Sports Exerc 2000; 32 (2): 518–25PubMedCrossRef
126.
Yquel RJ, Arsac LM, Thiaudière E, et al. Effect of creatine supplementation on phosphocreatine resynthesis, inorganic phosphate accumulation and pH during intermittent maximal exercise. J Sports Sci 2002; 20 (5): 427–37PubMedCrossRef
127.
Barnett C, Hinds M, Jenkins DG. Effects of oral creatine supplementation on multiple sprint cycle performance. Aust J Sci Med Sport 1996; 28 (1): 35–9PubMed
128.
Dawson B, Cutler M, Moody A, et al. Effects of oral creatine loading on single and repeated maximal short sprints. Aust J Sci Med Sport 1995; 27 (3): 56–61PubMed
129.
Delecluse C, Diels R, Goris M. Effect of creatine supplementation on intermittent sprint running performance in highly trained athletes. J Strength Cond Res 2003; 17 (3): 446–54PubMed
130.
Leenders NM, Lamb DR, Nelson TE. Creatine supplementation and swimming performance. Int J Sport Nutr 1999; 9 (3): 251–62PubMed
131.
McKenna MJ, Morton J, Selig SE, et al. Creatine supplementation increases muscle total creatine but not maximal intermittent exercise performance. J Appl Physiol 1999; 87 (6): 2244–52PubMed
132.
Cady EB, Jones DA, Lynn J, et al. Changes in force and intracellular metabolites during fatigue of human skeletal muscle. J Physiol 1989; 418: 311–25PubMed
133.
DeGroot M, Massie BM, Boska M, et al. Dissociation of [H+] from fatigue in human muscle detected by high time resolution 31P-NMR. Muscle Nerve 1993; 16 (1): 91–8PubMedCrossRef
134.
Miller RG, Boska MD, Moussavi RS, et al. 31P nuclear magnetic resonance studies of high energy phosphates and pH in human muscle fatigue: comparison of aerobic and anaerobic exercise. J Clin Invest 1988; 81 (4): 1190–6PubMedCrossRef
135.
Chase PB, Kushmerick MJ. Effects of pH on contraction of rabbit fast and slow skeletal muscle fibers. Biophys J 1988; 53 (6): 935–46PubMedCrossRef
136.
Cooke R, Franks K, Luciani GB, et al. The inhibition of rabbit skeletal muscle contraction by hydrogen ions and phosphate. J Physiol 1988; 395: 77–97PubMed
137.
Godt RE, Nosek TM. Changes of intracellular milieu with fatigue or hypoxia depress contraction of skinned rabbit skeletal and cardiac muscle. J Physiol 1989; 412: 155–80PubMed
138.
Kentish JC, Palmer S. Effect of pH on force and stiffness in skinned muscles isolated from rat and guinea-pig ventricle and from rabbit psoas muscle [abstract]. J Physiol 1989; 410: 67P
139.
Metzger JM, Moss RL. Greater hydrogen ion-induced depression of tension and velocity in skinned single fibres of rat fast than slow muscles. J Physiol 1987; 393: 727–42PubMed
140.
Bruton JD, Lannergren J, Westerblad H. Effects of CO2-induced acidification on the fatigue resistance of single mouse muscle fibers at 28 degrees C. J Appl Physiol 1998; 85 (2): 478–83PubMed
141.
Pate E, Bhimani M, Franks-Skiba K, et al. Reduced effect of pH on skinned rabbit psoas muscle mechanics at high temperatures: implications for fatigue. J Physiol 1995; 486 (3): 689–94PubMed
142.
Westerblad H, Bruton JD, Lännergren J. The effect of intracellular pH on contractile function of intact, single fibres of mouse muscle declines with increasing temperature. J Physiol 1997; 500 (1): 193–204PubMed
143.
Wiseman RW, Beck TW, Chase PB. Effect of intracellular pH on force development depends on temperature in intact skeletal muscle from mouse. Am J Physiol 1996; 271 (3): C878–86
144.
Linderman JK, Gosselink KL. The effects of sodium bicarbonate ingestion on exercise performance. Sports Med 1994; 18 (2): 75–80PubMedCrossRef
145.
Lavender G, Bird SR. Effect of sodium bicarbonate ingestion upon repeated sprints. Br J Sports Med 1989; 23 (1): 41–5PubMedCrossRef
146.
Bishop D, Edge J, Davis C, et al. Induced metabolic alkalosis affects muscle metabolism and repeated-sprint ability. Med Sci Sports Exerc 2004; 36 (5): 807–13PubMed
147.
Gaitanos GC, Nevill ME, Brooks S, et al. Repeated bouts of sprint running after induced alkalosis. J Sports Sci 1991; 9 (4): 355–70PubMedCrossRef
148.
Allen DG, Kabbara AA, Westerblad H. Muscle fatigue: the role of intracellular calcium stores. Can J Appl Physiol 2002; 27 (1): 83–96PubMedCrossRef
149.
Dahlstedt AJ, Katz A, Wieringa B, et al. Is creatine kinase responsible for fatigue? Studies of isolated skeletal muscle deficient in creatine kinase. FASEB J 2000; 14 (7): 982–90PubMed
150.
Dahlstedt AJ, Westerblad H. Inhibition of creatine kinase reduces the rate of fatigue-induced decrease in tetanic Ca2+ in mouse skeletal muscle. J Physiol 2001; 533 (3): 639–49PubMedCrossRef
151.
Fryer MW, Owen VJ, Lamb GD, et al. Effects of creatine phosphate and Pi on Ca2+ movements and tension development in rat skinned skeletal muscle fibres. J Physiol 1995; 482 (1): 123–40PubMed
152.
Kabbara AA, Allen DG. The role of calcium stores in fatigue of isolated single muscle fibres from the cane toad. J Physiol 1999; 519 (1): 169–76PubMedCrossRef
153.
Allen DG, Lee JA, Westerblad H. Intracellular calcium and tension during fatigue in isolated single muscle fibres from Xenopus laevis. J Physiol 1989; 415: 433–58PubMed
154.
Baker AJ, Kostov KG, Miller RG, et al. Slow force recovery after long duration exercise: metabolic and activation factors in muscle fatigue. J Appl Physiol 1993; 74: 2294–300PubMedCrossRef
155.
Gyorke S. Effects of repeated tetanic stimulation on excitation-contraction coupling in cut muscle fibres of the frog. J Physiol 1993; 464: 699–710PubMed
156.
Westerblad H, Lee JA, Lamb AG, et al. Spatial gradients of intracellular calcium in skeletal muscle during fatigue. Pflugers Arch 1990; 415 (6): 734–40PubMedCrossRef
157.
Duke AM, Steele DS. Mechanisms of reduced SR Ca2+ release induced by inorganic phosphate in rat skeletal muscle fibers. Am J Physiol 2001; 281: C418–29
158.
McLester Jr JR. Muscle contraction and fatigue: the role of adenosine 5’-diphosphate and inorganic phosphate. Sports Med 1997; 23 (5): 287–305PubMedCrossRef
159.
Posterino GS, Dutka TL, Lamb GD. L(+)-lactate does not affect twitch and tetanic responses in mechanically skinned mammalian muscle fibres. Pflugers Arch 2001; 442 (2): 197–203PubMedCrossRef
160.
Stackhouse SK, Reisman DS, Binder-Macleod SA. Challenging the role of pH in skeletal muscle fatigue. Phys Ther 2001; 81 (12): 1897–903PubMed
161.
Westerblad H, Allen DG, Lännergren J. Muscle fatigue: lactic acid or inorganic phosphate the major cause? News Physiol Sci 2002; 17: 17–21PubMed
162.
Cymerman A, Reeves JT, Sutton JR, et al. Operation Everest II: maximal oxygen uptake at extreme altitude. J Appl Physiol 1989; 66 (5): 2446–53PubMed
163.
Eiken O, Tesch PA. Effects of hyperoxia and hypoxia on dynamic and sustained static performance of the human quadriceps muscle. Acta Physiol Scand 1984; 122 (4): 629–33PubMedCrossRef
164.
Fulco CS, Lewis SF, Frykman PN, et al. Muscle fatigue and exhaustion during dynamic leg exercise in normoxia and hypobaric hypoxia. J Appl Physiol 1996; 81 (5): 1891–900PubMed
165.
Hogan MC, Kohin S, Stary CM, et al. Rapid force recovery in contracting skeletal muscle after brief ischemia is dependent on O2 availability. J Appl Physiol 1999; 87 (6): 2225–9PubMed
166.
Hogan MC, Richardson RS, Haseler LJ. Human muscle performance and PCr hydrolysis with varied inspired oxygen fractions: a 31P-MRS study. J Appl Physiol 1999; 86 (4): 1367–73PubMed
167.
Peltonen JE, Rantamaki J, Niittymaki SP, et al. Effects of oxygen fraction in inspired air on rowing performance. Med Sci Sports Exerc 1995; 27 (4): 573–9PubMed
168.
Balsom PD, Ekblom B, Sjödin B. Enhanced oxygen availability during high intensity intermittent exercise decreases anaerobic metabolite concentrations in blood. Acta Physiol Scand 1994; 150 (4): 455–6PubMedCrossRef
169.
Balsom PD, Gaitanos GC, Ekblom B, et al. Reduced oxygen availability during high intensity intermittent exercise impairs performance. Acta Physiol Scand 1994; 152 (3): 279–85PubMedCrossRef
170.
MacDonald M, Pedersen PK, Hughson RL. Acceleration of V-dotO2 kinetics in heavy submaximal exercise by hyperoxia and prior high-intensity exercise. J Appl Physiol 1997; 83 (4): 1318–25PubMed
171.
Hughson RL, Kowalchuk JM. Kinetics of oxygen uptake for submaximal exercise in hyperoxia, normoxia, and hypoxia. Can J Appl Physiol 1995; 20 (2): 198–210PubMedCrossRef
172.
Linnarsson D, Karlsson J, Fagraeus L. Muscle metabolites and oxygen deficit with exercise in hypoxia and hyperoxia. J Appl Physiol 1974; 36 (4): 399–402PubMed
173.
Pedersen PK. Oxygen uptake kinetics and lactate accumulation in heavy submaximal exercise with normal and high inspired oxygen fractions. In: Knuttgen HG, Vogel JA, Poortmans J, editors. Biochemistry of exercise, international series in sports science, vol. XIII. Champaign (IL): Human Kinetics, 1983: 415–20
174.
Aziz AR, Chia M, Teh KC. The relationship between maximal oxygen uptake and repeated sprint performance indices in field hockey and soccer players. J Sport Med Phys Fitness 2000; 40: 195–200
175.
Bell GJ, Snydmiller GD, Davies DS, et al. Relationship between aerobic fitness and metabolic recovery from intermittent exercise in endurance athletes. Can J Appl Physiol 1997; 22 (1): 78–85PubMedCrossRef
176.
Dawson B, Fitzsimons M, Ward D. The relationship of repeated sprint ability to aerobic power and performance measures of an aerobic work capacity and power. Aust J Sci Med Sport 1993; 25 (4): 88–93
177.
Tomlin DL, Wenger HA. The relationship between aerobic fitness and recovery from high intensity intermittent exercise. Sports Med 2001; 31 (1): 1–11PubMedCrossRef
178.
Carter H, Jones AM, Barstow TJ, et al. Effect of endurance training on oxygen uptake kinetics during treadmill running. J Appl Physiol 2000; 89 (5): 1744–52PubMed
179.
Chilibeck PD, Paterson DH, Petrella RJ, et al. The influence of age and cardiorespiratory fitness on kinetics of oxygen uptake. Can J Appl Physiol 1996; 21 (3): 185–96PubMedCrossRef
180.
Demarle AP, Slawinski JJ, Laffite LP, et al. Decrease of O2 deficit is a potential factor in increased time to exhaustion after specific endurance training. J Appl Physiol 2001; 90 (3): 947–53PubMed
181.
Norris SR, Petersen SR. Effects of endurance training on transient oxygen uptake responses in cyclists. J Sports Sci 1998; 16 (8): 733–8PubMedCrossRef
182.
Phillips SM, Green HJ, MacDonald MJ, et al. Progressive effect of endurance training on V-dotO2 kinetics at the onset of submaximal exercise. J Appl Physiol 1995; 79 (6): 1914–20PubMed
183.
Yoshida T, Udo M, Ohmori T, et al. Day-to-day changes in oxygen uptake kinetics at the onset of exercise during strenuous endurance training. Eur J Appl Physiol 1992; 64 (1): 78–83CrossRef
184.
McCully KK, Posner JD. Measuring exercise-induced adaptations and injury with magnetic resonance spectroscopy. Int J Sports Med 1992; 13: S147–9CrossRef
185.
Laurent D, Reutenauer H, Payen JF, et al. Muscle bioenergetics in skiers: studies using NMR spectroscopy. Int J Sports Med 1992; 13 (1): S150–2CrossRef
186.
McCully KK, Boden BP, Tuchler M, et al. Wrist flexor muscles of elite rowers measured with magnetic resonance spectroscopy. J Appl Physiol 1989; 67 (3): 926–32PubMed
187.
McCully KK, Vandenborne K, De Meirleir K, et al. Muscle metabolism in track athletes, using 31P magnetic resonance spectroscopy. Can J Physiol Pharmacol 1992; 70 (10): 1353–9PubMedCrossRef
188.
Yoshida T, Watari H. Metabolic consequences of repeated exercise in long distance runners. Eur J Appl Physiol 1993; 67 (3): 261–5CrossRef
189.
Freund H, Lonsdorfer J, Oyono-Enguelle S, et al. Lactate exchange and removal abilities in sickle cell patients and in untrained and trained healthy humans. J Appl Physiol 1992; 73 (6): 2580–7PubMed
190.
Oyono-Enguelle S, Marbach J, Heitz A, et al. Lactate removal ability and graded exercise in humans. J Appl Physiol 1990; 68 (3): 905–11PubMed
191.
Taoutaou Z, Granier P, Mercier B, et al. Lactate kinetics during passive and partially active recovery in endurance and sprint athletes. Eur J Appl Physiol 1996; 73 (5): 465–70CrossRef
192.
Bassett Jr DR, Merrill PW, Nagle FJ, et al. Rate of decline in blood lactate after cycling exercise in endurance-trained and untrained subjects. J Appl Physiol 1991; 70 (4): 1816–20PubMed
193.
Oosthuyse T, Carter RN. Plasma lactate decline during passive recovery from high-intensity exercise. Med Sci Sports Exerc 1999; 31 (5): 670–4PubMedCrossRef
194.
Evans BW, Cureton KJ. Effect of physical conditioning on blood lactate disappearance after supramaximal exercise. Br J Sports Med 1983; 17 (1): 40–5PubMedCrossRef
195.
Fukuba Y, Walsh ML, Morton RH, et al. Effect of endurance training on blood lactate clearance after maximal exercise. J Sports Sci 1999; 17 (3): 239–48PubMedCrossRef
196.
Donovan CM, Pagliassotti MJ. Enhanced efficiency of lactate removal after endurance training. J Appl Physiol 1990; 68 (3): 1053–8PubMed
197.
Helgerud J, Engen LC, Wisloff U, et al. Aerobic endurance training improves soccer performance. Med Sci Sports Exerc 2001; 33 (11): 1925–31PubMedCrossRef
198.
Bishop D, Lawrence S, Spencer M. Predictors of repeated-sprint ability in elite female hockey players. J Sci Med Sport 2003; 6 (2): 199–209PubMedCrossRef
199.
Wadley G, Le Rossignol P. The relationship between repeated sprint ability and the aerobic and anaerobic energy systems. J Sci Med Sport 1998; 1 (2): 100–10PubMedCrossRef
Metadaten
Titel
Multiple Sprint Work
Physiological Responses, Mechanisms of Fatigue and the Influence of Aerobic Fitness
verfasst von
Dr Mark Glaister
Publikationsdatum
01.09.2005
Verlag
Springer International Publishing
Erschienen in
Sports Medicine / Ausgabe 9/2005
Print ISSN: 0112-1642
Elektronische ISSN: 1179-2035
DOI
https://doi.org/10.2165/00007256-200535090-00003

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