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EFFECTS OF VARIOUS HYPOBARIC HYPOXIA ON METABOLIC RESPONSE, SKELETAL MUSCLE OXYGENATION, AND EXERCISE PERFORMANCE IN HEALTHY MALES

  • Jong-Beom Seo1
  • Sung-Woo Kim2
  • Won-Sang Jung2
  • Hun-Young Park1,2
  • Kiwon Lim1,2,3

1Department of Sports Medicine and Science, Konkuk University, Seoul, Republic of Korea

2Physical Activity and Performance Institute (PAPI), Konkuk University, Seoul, Republic of Korea

3Department of Physical Education, Konkuk University, Seoul, Republic of Korea

DOI: 10.31083/jomh.v16i4.312 Vol.16,Issue 4,October 2020 pp.107-120

Published: 01 October 2020

*Corresponding Author(s): Kiwon Lim E-mail: exercise@konkuk.ac.kr

Abstract

Objective

This study aimed to evaluate the effect of various levels of hypoxia versus normoxia on exercise perfor-mance, measured by metabolic parameters and skeletal muscle oxygenation profiles during graded exercise test (GXT) in healthy men.

Methods

In this randomized crossover trial, 11 healthy male participants (age 21.5 ± 2.3 years) performed the GXT using a cycle ergometer at sea-level (760 torr) and at various hypobaric hypoxia: 633, 526, and 433 torr, corresponding to simulated altitudes of 1500, 3000, and 4500 m, respectively. The GXT was started at 50 W and increased by 25 W every 2 min until the participants were exhausted. The pedal frequency was set to 60 rpm. Metabolic parameters (heart rate, HR; minute ventilation, VE; carbon dioxide excretion, VCO2; respiratory exchange ratio, RER; peripheral capillary saturation, SpO2; oxygen consumption, VO2; and blood lactate, O2 pulse) and skeletal muscle oxygen profiles (oxygenated hemoglobin and myoglobin, OxyHb; deoxygenated hemoglobin and myoglobin, DeoxyHb; and tissue oxygen saturation, StO2) were measured for every 2 min during the GXT. Exercise performance was evaluated by maximal oxygen con-sumption, peak power, and duration of exercise time obtained through GXT.

Results

Regarding metabolic parameters, HR (P < 0.05), VE, (P < 0.05), VCO2 (P < 0.05), RER (P < 0.05), and blood lactate (P < 0.05) showed significant increase under hypoxia compared to normoxia. Moreover, the increase was more pronounced as hypoxia became more severe. However, the SPO2 (P < 0.05) and O2 pulse (P < 0.05) presented a significant decrease under hypoxia compared to normoxia. Similarly, the decrease was more pronounced as hypoxia became more severe. VO2 (P > 0.05) did not show significant difference under different environmental conditions. In skeletal muscle oxygen profiles, none of the param-eters showed noticeable changes. Regarding exercise performance, VO2max (P < 0.05) and exercise time (P < 0.05) decreased significantly as hypoxia became more severe, and peak power (P < 0.05) decreased significantly at simulated altitudes of 3000 and 4500 m compared to normoxia.

Conclusion

A decrease in exercise performance is due to a decrease in metabolic function under various hypoxia compared to normoxia and the decrease was more pronounced as hypoxia became more severe.

Keywords

exercise performance; graded exercise test; hypoxia; metabolic function; NIRS; skeletal muscle oxygenation

Cite and Share

Jong-Beom Seo,Sung-Woo Kim,Won-Sang Jung,Hun-Young Park,Kiwon Lim. EFFECTS OF VARIOUS HYPOBARIC HYPOXIA ON METABOLIC RESPONSE, SKELETAL MUSCLE OXYGENATION, AND EXERCISE PERFORMANCE IN HEALTHY MALES. Journal of Men's Health. 2020. 16(4);107-120.

References

1. Bhaumik G, Dass D, Lama H, et al. Maximum exer-cise responses of men and women mountaineering trainees on induction to high altitude (4350 m) by trekking. Wilderness Environ Med. 2008;19(3): 151–6. https://doi.org/10.1580/07-WEME-OR-121.1

2. Brutsaert TD. Do high-altitude natives have enhanced exercise performance at altitude? Appl Physiol Nutr Metab. 2008;33(3):582–92. https://doi. org/10.1139/H08-009

3. DeLorey DS, Shaw CN, Shoemaker JK, et al. The effect of hypoxia on pulmonary O2 uptake, leg blood flow and muscle deoxygenation during single- leg knee-extension exercise. Exp Physiol. 2004; 89(3):293–302. https://doi.org/10.1113/expphysiol. 2003.026864

4. Moon HW, Sun OS, Park HY, et al. Effects of var-ious acute hypoxic conditions on metabolic param-eters and cardiac function during exercise and recovery. Springerplus. 2016;5(1):1294. https://doi. org/10.1186/s40064-016-2952-4

5. Mollard P, Woorons X, Letournel M, et al. Determinants of maximal oxygen uptake in mod-erate acute hypoxia in endurance athletes. Eur J Appl Physiol. 2007;100(6):663–73. https://doi. org/10.1007/s00421-007-0457-0

6. Wehrlin JP, Hallén J. Linear decrease in VO2max and performance with increasing altitude in endur-ance athletes. Eur J Appl Physiol. 2006;96(4):404–

12. https://doi.org/10.1007/s00421-005-0081-9

7. Nam SS, Sun OS. The change of muscle oxygen-ation and RBC deformabillity during submaximal exercise at various hypobaric condition. Korean Soc Sport Sci. 2011;20:1123–38.

8. Siebenmann C, Lundby C. Regulation of car-diac output in hypoxia. Scand J Med Sci Sport. 2015;25:53–9. https://doi.org/10.1111/sms.12619

9. Ofner M, Wonisch M, Frei M, et al. Influence of acute normobaric hypoxia on physiological vari-ables and lactate turn point determination in trained men. J Sport Sci Med. 2014;13(4):774–81.

10. Woorons X, Bourdillon N, Vandewalle H, et al. Exercise with hypoventilation induces lower mus-cle oxygenation and higher blood lactate concentra-tion: Role of hypoxia and hypercapnia. Eur J Appl Physiol. 2010;110(2):367–77. https://doi.org/10.1007/s00421-010-1512-9

11. Naeije R, Huez S, Lamotte M, et al. Pulmonary artery pressure limits exercise capacity at high alti-tude. Eur Respir J. 2010;36(5):1049–55. https://doi. org/10.1183/09031936.00024410

12. Thomson AJ, Drummond GB, Waring WS, et al. Effects of short-term isocapnic hyperoxia and hypoxia on cardiovascular function. J Appl Physiol. 2006;101(3):809–16. https://doi.org/10.1152/japplphysiol.01185.2005

13. Fukuda T, Maegawa T, Matsumoto A, et al. Effects of acute hypoxia at moderate altitude on stroke vol-ume and cardiac output during exercise. Int Heart J. 2010;51(3):170–5. https://doi/org/10.1536/ihj.51.170

14. Peltonen JE, Tikkanen HO, Rusko HK. Cardio-respiratory responses to exercise in acute hypoxia, hyperoxia and normoxia. Eur J Appl Physiol. 2001; 85(1–2):82–8. https://doi.org/10.1007/s004210100411

15. Moon HW, Shin SH, Lee CH, et al. Effects of vari-ous acute hypoxic conditions on the hemorheolog-ical response during exercise and recovery 1. Clin Hemorheol Microcirc. 2016;63(4):451–60. https://doi.org/10.3233/CH-16163

16. Jung WS, Kim SW, Park HY. Interval hypoxic train-ing enhances athletic performance and does not adversely affect immune function in middle-and long-distance runners. Int J Environ Res Public Health. 2020;17(6):1934. https://doi.org/10.3390/ijerph17061934

17. Bilski J, Teległów A, Pokorski J, et al. Effects of a meal on the hemorheologic responses to exercise in young males. Biomed Res Int. 2014;2014(Dm):5–9. https://doi.org/10.1155/2014/862968

18. Park HY, Park W, Lim K. Living high-training low for 21 days enhances exercise economy, hemodynamic function, and exercise performance of competitive runners. J Sport Sci Med. 2019;18(3):427–37.

19. Wang JS, Lee MY, Lien HY, et al. Hypoxic exercise training improves cardiac/muscular hemodynamics and is associated with modulated circulating progenitor cells in sedentary men. Int J Cardiol. 2014;170(3):315–

23. https://doi.org/10.1016/j.ijcard.2013.11.005

20. Bhambhani YN. Muscle oxygenation trends during dynamic exercise measured by near infrared spec-troscopy. Can J Appl Physiol. 2004;29(4):504–23. https://doi.org/10.1139/h04-033

21. Rupp T, Perrey S. Effect of severe hypoxia on prefrontal cortex and muscle oxygenation responses at rest and during exhaustive exercise. Adv Exp Med Biol. 2009;645:301–6. https://doi. org/10.1007/978-0-387-85998-9

22. Moon HW, Sun OS, Park HY, et al. The acid-base response during absolutely intensity exercise at var-ious normobaric hypoxic condition. Korea J Sport Sci. 2015;24(6):1175–88.

23. Nam SS, Moon HW, Park HY, et al. The property of gender, body composition, physical fitness level, ACE gene polymorphism on differneces of submax-imal exercise capacity at various hypobaric hypoxic condition. Exerc Sci. 2011;20(1):47–60. https://doi. org/10.15857/ksep.2011.20.1.47

24. Netzer NC, Rausch L, Eliasson AH, et al. SpO2 and heart rate during a real hike at altitude are signifi-cantly different than at its simulation in normobaric hypoxia. Front Physiol. 2017;8(Feb):1–9. https://doi. org/10.3389/fphys.2017.00081

25. Lundby C, Van Hall G. Substrate utilization in sea level residents during exercise in acute hypoxia and after 4 weeks of acclimatization to 4100 m. Acta Physiol Scand. 2002;176(3):195–201. https://doi. org/10.1046/j.1365-201X.2002.01030.x

26. Hill NE, Stacey MJ, Woods DR. Energy at high altitude. J R Army Med Corps. 2011;157(1):43–8. https://doi.org/10.1136/jramc-157-01-08

27. Kennedy MD, Warburton DER, Boliek CA, et al. The oxygen delivery response to acute hypoxia during incremental knee extension exercise differs in active and trained males. Dyn Med. 2008;7(1):1–

12. https://doi.org/10.1186/1476-5918-7-11

28. Griffiths A, Shannon OM, Matu J, et al. The effects of environmental hypoxia on substrate utilisation during exercise: A meta-analysis. J Int Soc Sports Nutr. 2019;16(1):1–14. https://doi.org/10.1186/s12970-019- 0277-8

29. Katayama K, Goto K, Ishida K, et al. Substrate uti-lization during exercise and recovery at moderate altitude. Metabolism. 2010;59(7):959–66. https://doi.org/10.1016/j.metabol.2009.10.017

30. Astorino TA, Rar FG. Acute hypoxia alters lac-tate threshold in chronic altitude residents. J Exer Physiol. 2004;2(1):6–15.

31. Benoit H, Busso T, Castells J, et al. Decrease in peak heart rate with acute hypoxia in relation to sea level VO2max. Eur J Appl Physiol. 2003;90(5–6):514–9. https://doi.org/10.1007/s00421-003-0899-y

32. Mazzeo RS. Physiological responses to exercise at altitude. Sport Med. 2008;38(1):1–8. https://doi. org/10.2165/00007256-200838010-00001

33. Zupet P, Princi T, Finderle Z. Effect of hypobaric hypoxia on heart rate variability during exercise: A pilot field study. Eur J Appl Physiol. 2009;107(3):345–

50. https://doi.org/10.1007/s00421-009-1123-5

34. Woorons X, Mollard P, Lamberto C,et al. Effect of acute hypoxia on maximal exercise in trained and sedentary women. Med Sci Sports Exerc. 2005;37(1): 147–54. https://doi.org/10.1249/01.mss.0000150020. 25153.34

35. Schoene RB. Limits of human lung function at high altitude. J Exp Biol. 2001;204(18):3121–7.

36. West JB. Limiting factors for exercise at extreme altitudes. Clin Physiol. 1990;10(3):265–72. https://doi.org/10.1111/j.1475-097x.1990.tb00095.x

37. Ozcelik O, Kelestimur H. Effects of acute hypoxia on the determination of anaerobic threshold using the heart rate-work rate relationships during incre-mental exercise tests. Physiol Res. 2004;53(1):45–51.

38. Benditt JO, Lewis S, Wood DE, et al. Lung volume reduction surgery improves maximal O2 consump-tion, maximal minute ventilation, O2 pulse, and dead space-to-tidal volume ratio during leg cycle ergom-etry. Am J Respir Crit Care Med. 1997;156(2 I):561–

6. https://doi.org/10.1164/ajrccm.156.2.9611032

39. Park HY, Nam SS. Application of “living high-train-ing low” enhances cardiac function and skeletal muscle oxygenation during submaximal exercises in athletes. J Exerc Nutr Biochem. 2017;21(1):13–20. https://doi.org/10.20463/jenb.2017.0064

40. Neary JP, McKenzie DC, Bhambhani YN. Effects of short-term endurance training on muscle deox-ygenation trends using NIRS. Med Sci Sports Exerc. 2002;34(11):1725–32. https://doi.org/10.1097/ 00005768-200211000-00006

41. Oguri K, Du N, Kato Y, et al. Effect of moderate altitude on peripheral muscle oxygenation during leg resistance exercise in young males. J Sport Sci Med. 2004;3(3):182–9.

42. Subudhi AW, Lorenz MC, Fulco CS, et al. Cerebrovascular responses to incremental exercise during hypobaric hypoxia: Effect of oxygenation on maximal performance. Am J Physiol Hear Circ Physiol. 2008;294(1):164–71. https://doi.org/10.1152/ajpheart.01104.2007

43. Sweeting AJ, Billaut F, Varley MC, et al. Variations in hypoxia impairs muscle oxygenation and perfor-mance during simulated team-sport running. Front Physiol. 2017;8(Feb):1–11. https://doi.org/10.3389/fphys.2017.00080

44. Subudhi AW, Miramon BR, Granger ME, et al. Frontal and motor cortex oxygenation during max-imal exercise in normoxia and hypoxia. J Appl Physiol. 2009;106(4):1153–8. https://doi.org/10.1152/japplphysiol.91475.2008

45. Amann M, Goodall S, Twomey R, Subudhi AW, Lovering AT, Roach RC. AltitudeOmics: On the consequences of high-altitude acclimatization for the development of fatigue during locomotor exer-cise in humans. J Appl Physiol. 2013;115(5):634–42. https://doi.org/10.1152/japplphysiol.00606.2013

46. Siebenmann CA. The impact of hypoxia on aerobic exercise capacity the impact of hypoxia on aerobic exercise capacity. 2012. https://www.zora.uzh.ch/id/eprint/71216/

47. Sun OS, Nam SS, Hwang KS, et al. The effects of intermittent hypobaric hypoxia exposure at the alti-tude of 3,000m on maximal oxygen uptake and oxy-gen transporting capacity in fin swimmers. Korea J Sport Sci. 2008;17(4):1065–76.

48. Calbet JAL, Boushel R, Rådegran G, et al. Determinants of maximal oxygen uptake in severe acute hypoxia. Am J Physiol Regul Integr Comp Physiol. 2003;284(3):291–303. https://doi. org/10.1152/ajpregu.00155.2002

49. Robach P, Calbet JAL, Thomsen JJ, et al. The ergo-genic effect of recombinant human erythropoietin on V̇ O2max depends on the severity of arterial hypoxemia. PLoS One. 2008;3(8):e2996. https://doi. org/10.1371/journal.pone.0002996

50. Saunders PU, Pyne DB, Gore CJ. Endurance train-ing at altitude. High Alt Med Biol. 2009;10(2):135–

48. https://doi.org/10.1089/ham.2008.1092

51. Burtscher M, Gatterer H, Kleinsasser A. Cardiorespiratory fitness of high altitude moun-taineers: The underestimated prerequisite. High Alt Med Biol. 2015;16(2):169–70. https://doi. org/10.1089/ham.2015.0021

52. Heinicke K, Heinicke I, Schmidt W. A three-week traditional altitude training increases hemo-globin mass and red cell volume in elite biathlon athletes. Int J Sports Med. 2005;26(5):350–5. https://10.1055/s-2004-821052

53. Park HY, Lim KW. The effects of aerobic exer-cise at hypoxic condition during 6 weeks on body composition, blood pressure, arterial stiffness, and blood lipid level in obese women. Int Sports Sci Med. 2017;1(1):1–5.

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