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Biology open2017; 6(7); 1035-1040; doi: 10.1242/bio.020388

The effects of moderate intensity training in a hypoxic environment on transcriptional responses in Thoroughbred horses.

Abstract: This study investigated the effects of six weeks of normobaric hypoxic training on transcriptional expression of the genes associated with mitochondrial and glycolytic activities in Thoroughbred horses. Eight horses were divided into two groups of four. They completed an identical incremental, moderate intensity training program, except that one group trained in a hypoxic chamber with 15% oxygen for 30 min on alternate days except Sundays (HT), while the other group trained in normal air (NC). Prior to and post training, heart rate and blood lactate were measured during an incremental treadmill test. Muscle biopsy samples were taken prior to and 24 h post the training period for qPCR analysis of mRNA changes in VEGF, PPARγ, HIF-1α, PGC-1α, COX4, AK3, LDH, PFK, PKm and SOD-2. No significant differences between the HT and NC were detected by independent-samples -test with Bonferroni correction for multiple comparisons (>0.05) in relative changes of mRNA abundance. There were no significant differences between groups for heart rate and blood lactate during the treadmill test. The outcomes indicated that this hypoxia training program did not cause a significant variation in basal level expression of the selected mRNAs in Thoroughbreds as compared with normoxic training.
Publication Date: 2017-07-15 PubMed ID: 28583927PubMed Central: PMC5550905DOI: 10.1242/bio.020388Google Scholar: Lookup
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  • Journal Article

Summary

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This research assessed the impact of training in low oxygen conditions on certain gene expressions in Thoroughbred horses. The study found no significant variations in the selected genes, heart rate and blood lactate levels with this kind of training compared to normal air training.

Research Method

  • The study involved eight Thoroughbred horses, equally divided into two groups. Both groups underwent a similar incremental moderate-intensity training program.
  • However, one group trained in a hypoxic chamber with only 15% oxygen for 30 minutes every alternate day except Sundays (known as the HT group) while the other group trained in normal air conditions (referred to as the NC group).
  • At the start and end of the training, measurements of heart rate and blood lactate were recorded during an incremental treadmill test for both groups.
  • Additionally, muscle biopsy samples were taken from the horses before and 24 hours after the training period. These were analyzed using qPCR to assess changes in the transcriptional expression of ten genes associated with mitochondrial and glycolytic activities.

Study Findings

  • The genes examined were; VEGF, PPARγ, HIF-1α, PGC-1α, COX4, AK3, LDH, PFK, PKm, and SOD-2.
  • The results showed no significant differences between the HT and NC groups in relative changes of mRNA abundance for the selected genes.
  • This was determined by an independent-samples t-test with Bonferroni correction for multiple comparisons.
  • Similarly, there were no significant differences between the two groups in heart rate and blood lactate levels during the treadmill test.

Conclusions

  • The study concluded that training in a hypoxic environment did not cause significant changes in the basal level expressions of the selected genes in Thoroughbred horses, in comparison to training in normal air conditions.
  • This suggests that hypoxic training, in the conditions set out in this study, might not have the enhanced performance benefits sometimes attributed to such training methods.

Cite This Article

APA
Davie AJ, Wen L, Cust ARE, Beavers R, Fyfe T, Zhou S. (2017). The effects of moderate intensity training in a hypoxic environment on transcriptional responses in Thoroughbred horses. Biol Open, 6(7), 1035-1040. https://doi.org/10.1242/bio.020388

Publication

ISSN: 2046-6390
NlmUniqueID: 101578018
Country: England
Language: English
Volume: 6
Issue: 7
Pages: 1035-1040

Researcher Affiliations

Davie, Allan J
  • Southern Cross University, School of Health and Human Sciences, Lismore, NSW 2480, Australia.
Wen, Li
  • Tianjin University of Sports, Tianjin Key Laboratory of Exercise Physiology and Sports Medicine, Tianjin 300381, China shi.zhou@scu.edu.au wenli34@hotmail.com.
Cust, Andrew R E
  • Ballarat Veterinary Practice, Ballarat, VIC 3350, Australia.
Beavers, Rosalind
  • Southern Cross University, School of Health and Human Sciences, Lismore, NSW 2480, Australia.
Fyfe, Tom
  • Pulford Air and Gas, Sydney, NSW 2141, Australia.
Zhou, Shi
  • Southern Cross University, School of Health and Human Sciences, Lismore, NSW 2480, Australia shi.zhou@scu.edu.au wenli34@hotmail.com.

Conflict of Interest Statement

Competing interestsThe authors declare no competing or financial interests.

References

This article includes 34 references
  1. Abe T, Kitaoka Y, Kikuchi DM, Takeda K, Numata O, Takemasa T. High-intensity interval training-induced metabolic adaptation coupled with an increase in Hif-1α and glycolytic protein expression.. J Appl Physiol (1985) 2015 Dec 1;119(11):1297-302.
  2. Bailey DM, Davies B, Romer L, Castell L, Newsholme E, Gandy G. Implications of moderate altitude training for sea-level endurance in elite distance runners.. Eur J Appl Physiol Occup Physiol 1998 Sep;78(4):360-8.
    doi: 10.1007/s004210050432pubmed: 9754977google scholar: lookup
  3. Bergstrom J. Percutaneous needle biopsy of skeletal muscle in physiological and clinical research.. Scand J Clin Lab Invest 1975 Nov;35(7):609-16.
    doi: 10.3109/00365517509095787pubmed: 1108172google scholar: lookup
  4. Bigham AW, Lee FS. Human high-altitude adaptation: forward genetics meets the HIF pathway.. Genes Dev 2014 Oct 15;28(20):2189-204.
    doi: 10.1101/gad.250167.114pmc: PMC4201282pubmed: 25319824google scholar: lookup
  5. Chung D.-S., Lee J.-K., Kim Y.-S., Park D.-H., Sung B.-J., Cho N.-H., Oh I.-S.. Effects of intermittent normobaric hypoxia on oxidative stress during a period of endurance training.. Int. J. Appl. Sports Sci. 17, 59-71.
  6. Dundas J, Ling M. Reference genes for measuring mRNA expression.. Theory Biosci 2012 Dec;131(4):215-23.
    doi: 10.1007/s12064-012-0152-5pubmed: 22588998google scholar: lookup
  7. Egan B, O'Connor PL, Zierath JR, O'Gorman DJ. Time course analysis reveals gene-specific transcript and protein kinetics of adaptation to short-term aerobic exercise training in human skeletal muscle.. PLoS One 2013;8(9):e74098.
  8. Eivers SS, McGivney BA, Fonseca RG, MacHugh DE, Menson K, Park SD, Rivero JL, Taylor CT, Katz LM, Hill EW. Alterations in oxidative gene expression in equine skeletal muscle following exercise and training.. Physiol Genomics 2010 Jan 8;40(2):83-93.
  9. Faiss R, Léger B, Vesin JM, Fournier PE, Eggel Y, Dériaz O, Millet GP. Significant molecular and systemic adaptations after repeated sprint training in hypoxia.. PLoS One 2013;8(2):e56522.
  10. Friedmann-Bette B. Classical altitude training.. Scand J Med Sci Sports 2008 Aug;18 Suppl 1:11-20.
  11. Gore CJ, Hahn AG, Aughey RJ, Martin DT, Ashenden MJ, Clark SA, Garnham AP, Roberts AD, Slater GJ, McKenna MJ. Live high:train low increases muscle buffer capacity and submaximal cycling efficiency.. Acta Physiol Scand 2001 Nov;173(3):275-86.
  12. Greene H. M., Wickler S. J.. Acute altitude exposure (3800 meters) and metabolic capacity in the middle gluteal muscle of equids.. J. Equine Vet. Sci. 20, 194-197.
  13. Holliss BA, Fulford J, Vanhatalo A, Pedlar CR, Jones AM. Influence of intermittent hypoxic training on muscle energetics and exercise tolerance.. J Appl Physiol (1985) 2013 Mar 1;114(5):611-9.
  14. Hoppeler H, Vogt M. Muscle tissue adaptations to hypoxia.. J Exp Biol 2001 Sep;204(Pt 18):3133-9.
    pubmed: 11581327doi: 10.1242/jeb.204.18.3133google scholar: lookup
  15. Hoppeler H, Klossner S, Vogt M. Training in hypoxia and its effects on skeletal muscle tissue.. Scand J Med Sci Sports 2008 Aug;18 Suppl 1:38-49.
  16. Jensen K., Nielsen T. S., Fiskestrand A., Lund J. O., Christensen N. J., Sechef N. H.. High-altitude training does not increase maximal oxygen uptake or work capacity at sea level in rowers.. Scand. J. Med. Sci. Sports 3, 256-262.
  17. Little JP, Safdar A, Bishop D, Tarnopolsky MA, Gibala MJ. An acute bout of high-intensity interval training increases the nuclear abundance of PGC-1α and activates mitochondrial biogenesis in human skeletal muscle.. Am J Physiol Regul Integr Comp Physiol 2011 Jun;300(6):R1303-10.
    doi: 10.1152/ajpregu.00538.2010pubmed: 21451146google scholar: lookup
  18. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.. Methods 2001 Dec;25(4):402-8.
    doi: 10.1006/meth.2001.1262pubmed: 11846609google scholar: lookup
  19. Lui MA, Mahalingam S, Patel P, Connaty AD, Ivy CM, Cheviron ZA, Storz JF, McClelland GB, Scott GR. High-altitude ancestry and hypoxia acclimation have distinct effects on exercise capacity and muscle phenotype in deer mice.. Am J Physiol Regul Integr Comp Physiol 2015 May 1;308(9):R779-91.
    doi: 10.1152/ajpregu.00362.2014pmc: PMC4421747pubmed: 25695288google scholar: lookup
  20. Lundby C, Calbet JA, Robach P. The response of human skeletal muscle tissue to hypoxia.. Cell Mol Life Sci 2009 Nov;66(22):3615-23.
    doi: 10.1007/s00018-009-0146-8pubmed: 19756383google scholar: lookup
  21. McDonald J. H.. Handbook of Biological Statistics.. Baltimore, Maryland: Sparky House Publishing.
  22. Nagahisa H, Mukai K, Ohmura H, Takahashi T, Miyata H. Effect of High-Intensity Training in Normobaric Hypoxia on Thoroughbred Skeletal Muscle.. Oxid Med Cell Longev 2016;2016:1535367.
    doi: 10.1155/2016/1535367pmc: PMC5046030pubmed: 27721912google scholar: lookup
  23. Perry CG, Lally J, Holloway GP, Heigenhauser GJ, Bonen A, Spriet LL. Repeated transient mRNA bursts precede increases in transcriptional and mitochondrial proteins during training in human skeletal muscle.. J Physiol 2010 Dec 1;588(Pt 23):4795-810.
  24. Pilegaard H, Saltin B, Neufer PD. Exercise induces transient transcriptional activation of the PGC-1alpha gene in human skeletal muscle.. J Physiol 2003 Feb 1;546(Pt 3):851-8.
  25. Pinilla O. C. V.. Exercise and training at altitudes: Physiological effects and protocols.. Rev. Cienc. Salud 12, 111-126.
  26. Ponsot E, Dufour SP, Zoll J, Doutrelau S, N'Guessan B, Geny B, Hoppeler H, Lampert E, Mettauer B, Ventura-Clapier R, Richard R. Exercise training in normobaric hypoxia in endurance runners. II. Improvement of mitochondrial properties in skeletal muscle.. J Appl Physiol (1985) 2006 Apr;100(4):1249-57.
  27. Robach P, Bonne T, Flück D, Bürgi S, Toigo M, Jacobs RA, Lundby C. Hypoxic training: effect on mitochondrial function and aerobic performance in hypoxia.. Med Sci Sports Exerc 2014 Oct;46(10):1936-45.
    doi: 10.1249/MSS.0000000000000321pubmed: 24674976google scholar: lookup
  28. Rogers B.. Australian Racing Board investigates hypoxic trainingnPerformance Genetics.nwww.performancegenetics.com/single-post/2014/04/08/Australian-Racing-Board-investigates-Hypoxic-Training.. .
  29. Scott GR, Elogio TS, Lui MA, Storz JF, Cheviron ZA. Adaptive Modifications of Muscle Phenotype in High-Altitude Deer Mice Are Associated with Evolved Changes in Gene Regulation.. Mol Biol Evol 2015 Aug;32(8):1962-76.
    doi: 10.1093/molbev/msv076pmc: PMC4592356pubmed: 25851956google scholar: lookup
  30. Tariq N, Basharat Z, Butt S, Baig DN. Distribution analysis of profilin isoforms at transcript resolution with mRNA-seq and secondary structure in various organs of Rattus norvegicus.. Gene 2016 Sep 1;589(1):49-55.
    doi: 10.1016/j.gene.2016.05.023pubmed: 27185630google scholar: lookup
  31. Vogt M, Puntschart A, Geiser J, Zuleger C, Billeter R, Hoppeler H. Molecular adaptations in human skeletal muscle to endurance training under simulated hypoxic conditions.. J Appl Physiol (1985) 2001 Jul;91(1):173-82.
    pubmed: 11408428doi: 10.1152/jappl.2001.91.1.173google scholar: lookup
  32. Wickler SJ, Anderson TP. Hematological changes and athletic performance in horses in response to high altitude (3,800 m).. Am J Physiol Regul Integr Comp Physiol 2000 Oct;279(4):R1176-81.
  33. Williams R. S., Neufer P. D.. Regulation of gene expression in skeletal muscle by contractile activity.. The Handbook of Physiology: Exercise: Regulation and Integration of Multiple Systems pp. 1124-1150. Bethesda, MD: John Wiley & Sons, Inc..
  34. Zoll J, Ponsot E, Dufour S, Doutreleau S, Ventura-Clapier R, Vogt M, Hoppeler H, Richard R, Flück M. Exercise training in normobaric hypoxia in endurance runners. III. Muscular adjustments of selected gene transcripts.. J Appl Physiol (1985) 2006 Apr;100(4):1258-66.

Citations

This article has been cited 3 times.
  1. Davie A, Beavers R, Hargitaiová K, Denham J. The Emerging Role of Hypoxic Training for the Equine Athlete. Animals (Basel) 2023 Sep 3;13(17).
    doi: 10.3390/ani13172799pubmed: 37685063google scholar: lookup
  2. Mukai K, Ohmura H, Takahashi Y, Kitaoka Y, Takahashi T. Four weeks of high-intensity training in moderate, but not mild hypoxia improves performance and running economy more than normoxic training in horses. Physiol Rep 2021 Feb;9(4):e14760.
    doi: 10.14814/phy2.14760pubmed: 33611843google scholar: lookup
  3. Mukai K, Ohmura H, Matsui A, Aida H, Takahashi T, Jones JH. High-intensity training in normobaric hypoxia enhances exercise performance and aerobic capacity in Thoroughbred horses: A randomized crossover study. Physiol Rep 2020 May;8(10):e14442.
    doi: 10.14814/phy2.14442pubmed: 32441408google scholar: lookup