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Acute exercise does not induce an acute phase response (APR) in Standardbred trotters.

Abstract: The purpose of the study was to investigate whether acute strenuous exercise (1600- to 2500-m race) would elicit an acute phase response (APR) in Standardbred trotters. Blood levels of several inflammatory markers [serum amyloid A (SAA), haptoglobin, fibrinogen, white blood cell count (WBC), and iron], muscle enzymes [creatinine kinase (CK) and aspartate transaminase (AST)], and hemoglobin were assessed in 58 Standardbred trotters before and after racing. Hemoglobin levels increased and iron levels decreased 12 to 14 h after racing and haptoglobin concentrations, white blood cell counts, and iron levels were decreased 2 and/or 7 d after racing. Concentrations of CK, AST, SAA, and fibrinogen were unaltered in response to racing. Acute strenuous exercise did not elicit an acute phase reaction. The observed acute increase in hemoglobin levels and decreases in haptoglobin and iron levels may have been caused by exercise-induced hemolysis, which indicates that horses might experience a condition similar to athlete's anemia in humans. The pathogenesis and clinical implications of the hematological and blood-biochemical changes elicited by acute exercise in Standardbred trotters in the present study warrant further investigation. L’objectif de la présente étude est d’investiguer l’effet de l’exercice intensif (1600–2500 m) sur l’apparition d’une phase inflammatoire aigué chez des trotteurs. Les taux sanguins de différents marqueurs inflammatoires [serum amyloid A (SAA), haptoglobine, fibrinogène, globules blanc (WBC) et fer], d’enzymes musculaires [creatinine kinase (CK) et aspartate transaminase (AST)] et d’hémoglobine ont été évalué dans 58 trotteurs avant et après la course. Respectivement une augmentation et diminution des taux d’hémoglobine et de fer furent présente 12–14 heures suivant la course. Une réduction des taux d’haptoglobine, de globules blanc et de fer était présente 2 et/ou 7 jours après la course. Aucun changement dans les concentrations de CK, AST, SAA et fibrinogène n’a pu être démontre en relation avec la course.L’exercice intense réalise lors de cette étude n’a pu induire de phase inflammatoire aigué. L’augmentation d’hémoglobine et la diminution d’haptoglobine et de fer peuvent être causées par une hémolyse induite par l’exercice, indiquant qu’une condition similaire à l’anémie de l’athlète chez l’homme existe chez le cheval. La pathogénèse et l’implication clinique des modifications hématologiques et biochimiques lié à un exercice intense chez les trotteurs dans la présente étude justifié de plus amples investigations.(Traduit par Docteur Denis Verwilghen).
Publication Date: 2014-04-02 PubMed ID: 24688170PubMed Central: PMC3962284
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article investigates whether intense physical activity can trigger an acute phase response, an immune system reaction, in Standardbred trotters. The results indicated that racing didn’t induce an acute phase response, but did show a change in blood markers that could suggest a condition akin to athlete’s anemia.

Study Objective and Methodology

  • The primary aim of this research was to determine if acute strenuous exercise, such as a 1600- to 2500-m race, would initiate an acute phase response (APR) in Standardbred trotters. APR is a systemic response by the immune system to injury, infection, or inflammation.
  • The investigators observed the blood levels of several inflammation markers, muscle enzymes, and hemoglobin in 58 Standardbred trotters both before and after racing.

Key Findings

  • Results showed that hemoglobin levels increased while iron levels decreased 12 to 14 hours after racing.
  • Haptoglobin concentrations, white blood cell counts, and iron levels fell 2 and/or 7 days after the race.
  • Levels of creatinine kinase (CK), aspartate transaminase (AST), serum amyloid A (SAA), and fibrinogen remained unchanged in response to the race.
  • Importantly, the study found that acute strenuous exercise did not cause an acute phase response in the horses.

Potential Interpretations and Future Research

  • The acute increase in hemoglobin levels and decreases in haptoglobin and iron levels may stem from exercise-induced hemolysis, a breakdown of red blood cells which releases hemoglobin.
  • This finding suggests that horses might suffer from a condition similar to athlete’s anemia in humans, where intensive training leads to a decrease in the oxygen-carrying capacity of the blood.
  • The researchers conclude that further investigation is needed to fully understand the clinical implications and the physiological process of blood and biochemical changes elicited by acute exercise in Standardbred trotters.

Cite This Article

APA
Kristensen L, Buhl R, Nostell K, Bak L, Petersen E, Lindholm M, Jacobsen S. (2014). Acute exercise does not induce an acute phase response (APR) in Standardbred trotters. Can J Vet Res, 78(2), 97-102.

Publication

ISSN: 1928-9022
NlmUniqueID: 8607793
Country: Canada
Language: English
Volume: 78
Issue: 2
Pages: 97-102

Researcher Affiliations

Kristensen, Lena
  • Holstebro Equine Practice, Vinderup, Denmark (Kristensen); Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark (Buhl, Bak, Petersen, Lindholm, Jacobsen); Department of Clinical Sciences, Faculty of Veterinary Medicine and Animal Science, Swedish University of Agricultural Sciences, Uppsala, Sweden (Nostell).
Buhl, Rikke
  • Holstebro Equine Practice, Vinderup, Denmark (Kristensen); Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark (Buhl, Bak, Petersen, Lindholm, Jacobsen); Department of Clinical Sciences, Faculty of Veterinary Medicine and Animal Science, Swedish University of Agricultural Sciences, Uppsala, Sweden (Nostell).
Nostell, Katarina
  • Holstebro Equine Practice, Vinderup, Denmark (Kristensen); Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark (Buhl, Bak, Petersen, Lindholm, Jacobsen); Department of Clinical Sciences, Faculty of Veterinary Medicine and Animal Science, Swedish University of Agricultural Sciences, Uppsala, Sweden (Nostell).
Bak, Lars
  • Holstebro Equine Practice, Vinderup, Denmark (Kristensen); Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark (Buhl, Bak, Petersen, Lindholm, Jacobsen); Department of Clinical Sciences, Faculty of Veterinary Medicine and Animal Science, Swedish University of Agricultural Sciences, Uppsala, Sweden (Nostell).
Petersen, Ellen
  • Holstebro Equine Practice, Vinderup, Denmark (Kristensen); Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark (Buhl, Bak, Petersen, Lindholm, Jacobsen); Department of Clinical Sciences, Faculty of Veterinary Medicine and Animal Science, Swedish University of Agricultural Sciences, Uppsala, Sweden (Nostell).
Lindholm, Maria
  • Holstebro Equine Practice, Vinderup, Denmark (Kristensen); Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark (Buhl, Bak, Petersen, Lindholm, Jacobsen); Department of Clinical Sciences, Faculty of Veterinary Medicine and Animal Science, Swedish University of Agricultural Sciences, Uppsala, Sweden (Nostell).
Jacobsen, Stine
  • Holstebro Equine Practice, Vinderup, Denmark (Kristensen); Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark (Buhl, Bak, Petersen, Lindholm, Jacobsen); Department of Clinical Sciences, Faculty of Veterinary Medicine and Animal Science, Swedish University of Agricultural Sciences, Uppsala, Sweden (Nostell).

MeSH Terms

  • Acute-Phase Reaction / immunology
  • Animals
  • Aspartate Aminotransferases / blood
  • Creatine Kinase / blood
  • Female
  • Fibrinogen / metabolism
  • Haptoglobins / analysis
  • Hemoglobins / analysis
  • Horses / blood
  • Horses / immunology
  • Horses / physiology
  • Iron / blood
  • Leukocyte Count / veterinary
  • Linear Models
  • Male
  • Physical Conditioning, Animal / physiology
  • Serum Amyloid A Protein / analysis

References

This article includes 37 references
  1. Gabay C, Kushner I. Acute-phase proteins and other systemic responses to inflammation.. N Engl J Med 1999 Feb 11;340(6):448-54.
    pubmed: 9971870doi: 10.1056/nejm199902113400607google scholar: lookup
  2. Jacobsen S, Andersen PH. The acute phase protein serum amyloid A (SAA) as a marker of inflammation in horses.. Eq Vet Edu 2007;19:38–46.
  3. Peeling P. Exercise as a mediator of hepcidin activity in athletes.. Eur J Appl Physiol 2010 Nov;110(5):877-83.
    pubmed: 20697906doi: 10.1007/s00421-010-1594-4google scholar: lookup
  4. Oliveira-Filho JP, Badial PR, Cunha PH, Peiró JR, Araújo JP Jr, Divers TJ, Winand NJ, Borges AS. Lipopolysaccharide infusion up-regulates hepcidin mRNA expression in equine liver.. Innate Immun 2012 Jun;18(3):438-46.
    pubmed: 21926164doi: 10.1177/1753425911420181google scholar: lookup
  5. Cywinska A, Gorecka R, Szarska E, Witkowski L, Dziekan P, Schollenberger A. Serum amyloid A level as a potential indicator of the status of endurance horses.. Equine Vet J Suppl 2010 Nov;(38):23-7.
  6. Cywińska A, Szarska E, Górecka R, Witkowski L, Hecold M, Bereznowski A, Schollenberger A, Winnicka A. Acute phase protein concentrations after limited distance and long distance endurance rides in horses.. Res Vet Sci 2012 Dec;93(3):1402-6.
    pubmed: 22390917doi: 10.1016/j.rvsc.2012.02.008google scholar: lookup
  7. Kasapis C, Thompson PD. The effects of physical activity on serum C-reactive protein and inflammatory markers: a systematic review.. J Am Coll Cardiol 2005 May 17;45(10):1563-9.
    pubmed: 15893167doi: 10.1016/j.jacc.2004.12.077google scholar: lookup
  8. Drenth JP, Krebbers RJ, Bijzet J, van der Meer JW. Increased circulating cytokine receptors and ex vivo interleukin-1 receptor antagonist and interleukin-1beta production but decreased tumour necrosis factor-alpha production after a 5-km run.. Eur J Clin Invest 1998 Oct;28(10):866-72.
  9. Strachan AF, Noakes TD, Kotzenberg G, Nel AE, de Beer FC. C reactive protein concentrations during long distance running.. Br Med J (Clin Res Ed) 1984 Nov 10;289(6454):1249-51.
    pmc: PMC1443523pubmed: 6437505doi: 10.1136/bmj.289.6454.1249google scholar: lookup
  10. Wakshlag JJ, Kraus MS, Gelzer AR, Downey RL, Vacchani P. The influence of high-intensity moderate duration exercise on cardiac troponin I and C-reactive protein in sled dogs.. J Vet Intern Med 2010 Nov-Dec;24(6):1388-92.
  11. Giori L, Moretti P, Giordano A, Paltrinieri S. Short-term evaluation of serum amyloid A after exercise in clinically healthy horses.. J Eq Vet Sci 2011;31:499–501.
  12. Taylor C, Rogers G, Goodman C, Baynes RD, Bothwell TH, Bezwoda WR, Kramer F, Hattingh J. Hematologic, iron-related, and acute-phase protein responses to sustained strenuous exercise.. J Appl Physiol (1985) 1987 Feb;62(2):464-9.
    pubmed: 2435698doi: 10.1152/jappl.1987.62.2.464google scholar: lookup
  13. Weight LM, Alexander D, Jacobs P. Strenuous exercise: analogous to the acute-phase response?. Clin Sci (Lond) 1991 Nov;81(5):677-83.
    pubmed: 1721863doi: 10.1042/cs0810677google scholar: lookup
  14. Liesen H, Dufaux B, Hollmann W. Modifications of serum glycoproteins the days following a prolonged physical exercise and the influence of physical training.. Eur J Appl Physiol Occup Physiol 1977 Dec 22;37(4):243-54.
    pubmed: 74333doi: 10.1007/bf00430954google scholar: lookup
  15. Fazio F, Assenza A, Tosto F, Casella S, Piccione G, Caola G. Modifications of some acute phase proteins and the white blood cell count in thoroughbreds during training.. Vet Rec 2010 Sep 4;167(10):370-3.
    pubmed: 20817897doi: 10.1136/vr.c3761google scholar: lookup
  16. Jacobsen S, Kjelgaard-Hansen M, Hagbard Petersen H, Jensen AL. Evaluation of a commercially available human serum amyloid A (SAA) turbidometric immunoassay for determination of equine SAA concentrations.. Vet J 2006 Sep;172(2):315-9.
    pubmed: 15950503doi: 10.1016/j.tvjl.2005.04.021google scholar: lookup
  17. Pihl TH, Andersen PH, Kjelgaard-Hansen M, Mørck NB, Jacobsen S. Serum amyloid A and haptoglobin concentrations in serum and peritoneal fluid of healthy horses and horses with acute abdominal pain.. Vet Clin Pathol 2013 Jun;42(2):177-83.
    pubmed: 23577834doi: 10.1111/vcp.12031google scholar: lookup
  18. Jacobsen S, Nielsen JV, Kjelgaard-Hansen M, Toelboell T, Fjeldborg J, Halling-Thomsen M, Martinussen T, Thoefner MB. Acute phase response to surgery of varying intensity in horses: a preliminary study.. Vet Surg 2009 Aug;38(6):762-9.
  19. Nunokawa Y, Fujinaga T, Taira T, Okumura M, Yamashita K, Tsunoda N, Hagio M. Evaluation of serum amyloid A protein as an acute-phase reactive protein in horses.. J Vet Med Sci 1993 Dec;55(6):1011-6.
    pubmed: 7509640doi: 10.1292/jvms.55.1011google scholar: lookup
  20. Andersen SA, Petersen HH, Ersbøll AK, Falk-Rønne J, Jacobsen S. Vaccination elicits a prominent acute phase response in horses.. Vet J 2012 Feb;191(2):199-202.
    pubmed: 21371917doi: 10.1016/j.tvjl.2011.01.019google scholar: lookup
  21. Fazio F, Assenza A, Tosto F, Casella S, Piccione G, Caola G. Training and haematochemical profile in Thoroughbreds and Standardbreds: A longitudinal study.. Livest Sci 2011;141:221–226.
  22. Jacobsen S, Niewold TA, Halling-Thomsen M, Nanni S, Olsen E, Lindegaard C, Andersen PH. Serum amyloid A isoforms in serum and synovial fluid in horses with lipopolysaccharide-induced arthritis.. Vet Immunol Immunopathol 2006 Apr 15;110(3-4):325-30.
    pubmed: 16337010doi: 10.1016/j.vetimm.2005.10.012google scholar: lookup
  23. Walsh NP, Gleeson M, Shephard RJ, Gleeson M, Woods JA, Bishop NC, Fleshner M, Green C, Pedersen BK, Hoffman-Goetz L, Rogers CJ, Northoff H, Abbasi A, Simon P. Position statement. Part one: Immune function and exercise.. Exerc Immunol Rev 2011;17:6-63.
    pubmed: 21446352
  24. Lejeune JP, Sandersen C, Votion D, Caudron I, Vander Heyden L, Franck T, Ceusters J, Mouithys-Mickalad A, Niesten A, De La Rebière de Pouyade G, Serteyn D. Effect of intensive exercise on plasmatic neutrophil elastase level in eventing and endurance horses.. Equine Vet J Suppl 2010 Nov;(38):12-6.
  25. Peeling P, Dawson B, Goodman C, Landers G, Trinder D. Athletic induced iron deficiency: new insights into the role of inflammation, cytokines and hormones.. Eur J Appl Physiol 2008 Jul;103(4):381-91.
    pubmed: 18365240doi: 10.1007/s00421-008-0726-6google scholar: lookup
  26. Inoue Y, Matsui A, Asai Y, Aoki F, Matsui T, Yano H. Effect of exercise on iron metabolism in horses.. Biol Trace Elem Res 2005 Oct;107(1):33-42.
    pubmed: 16170220doi: 10.1385/bter:107:1:033google scholar: lookup
  27. Paulev PE, Jordal R, Pedersen NS. Dermal excretion of iron in intensely training athletes.. Clin Chim Acta 1983 Jan 7;127(1):19-27.
    pubmed: 6825307doi: 10.1016/0009-8981(83)90071-2google scholar: lookup
  28. Dufaux B, Hoederath A, Streitberger I, Hollmann W, Assmann G. Serum ferritin, transferrin, haptoglobin, and iron in middle- and long-distance runners, elite rowers, and professional racing cyclists.. Int J Sports Med 1981 Feb;2(1):43-6.
    pubmed: 7333734doi: 10.1055/s-2008-1034583google scholar: lookup
  29. Buckman MT. Gastrointestinal bleeding in long-distance runners.. Ann Intern Med 1984 Jul;101(1):127-8.
    pubmed: 6610376doi: 10.7326/0003-4819-101-1-127google scholar: lookup
  30. Cordova Martinez A, Escanero JF. Iron, transferrin, and haptoglobin levels after a single bout of exercise in men.. Physiol Behav 1992 Apr;51(4):719-22.
    pubmed: 1594669doi: 10.1016/0031-9384(92)90107-dgoogle scholar: lookup
  31. Peeling P, Dawson B, Goodman C, Landers G, Wiegerinck ET, Swinkels DW, Trinder D. Training surface and intensity: inflammation, hemolysis, and hepcidin expression.. Med Sci Sports Exerc 2009 May;41(5):1138-45.
    pubmed: 19346972doi: 10.1249/mss.0b013e318192ce58google scholar: lookup
  32. Peeling P, Dawson B, Goodman C, Landers G, Wiegerinck ET, Swinkels DW, Trinder D. Cumulative effects of consecutive running sessions on hemolysis, inflammation and hepcidin activity.. Eur J Appl Physiol 2009 May;106(1):51-9.
    pubmed: 19184087doi: 10.1007/s00421-009-0988-7google scholar: lookup
  33. Telford RD, Sly GJ, Hahn AG, Cunningham RB, Bryant C, Smith JA. Footstrike is the major cause of hemolysis during running.. J Appl Physiol (1985) 2003 Jan;94(1):38-42.
  34. Yusof A, Leithauser RM, Roth HJ, Finkernagel H, Wilson MT, Beneke R. Exercise-induced hemolysis is caused by protein modification and most evident during the early phase of an ultraendurance race.. J Appl Physiol (1985) 2007 Feb;102(2):582-6.
  35. Allen B, Archer RK. Haptoglobins in the horse.. Vet Rec 1971 Jul 24;89(4):106-9.
    pubmed: 5558569doi: 10.1136/vr.89.4.106google scholar: lookup
  36. Cywinska A, Szarska E, Kowalska A, Ostaszewski P, Schollenberger A. Gender differences in exercise--induced intravascular haemolysis during race training in thoroughbred horses.. Res Vet Sci 2011 Feb;90(1):133-7.
    pubmed: 20553886doi: 10.1016/j.rvsc.2010.05.004google scholar: lookup
  37. Chatard JC, Mujika I, Guy C, Lacour JR. Anaemia and iron deficiency in athletes. Practical recommendations for treatment.. Sports Med 1999 Apr;27(4):229-40.

Citations

This article has been cited 11 times.
  1. Bollinger L, Bartel A, Weber C, Gehlen H. Pre-Ride Biomarkers and Endurance Horse Welfare: Analyzing the Impact of the Elimination of Superoxide Dismutase, δ-Aminolevulinic-Dehydratase, Thiobarbituric Acid Reactive Substances, Iron, and Serum Amyloid A Levels in Elite 160 km Endurance Rides. Animals (Basel) 2023 May 17;13(10).
    doi: 10.3390/ani13101670pubmed: 37238102google scholar: lookup
  2. Grzędzicka J, Dąbrowska I, Malin K, Witkowska-Piłaszewicz O. Exercise-related changes in the anabolic index (testosterone to cortisol ratio) and serum amyloid A concentration in endurance and racehorses at different fitness levels. Front Vet Sci 2023;10:1148990.
    doi: 10.3389/fvets.2023.1148990pubmed: 37138908google scholar: lookup
  3. Nemec Svete A, Vovk T, Bohar Topolovec M, Kruljc P. Effects of Vitamin E and Coenzyme Q(10) Supplementation on Oxidative Stress Parameters in Untrained Leisure Horses Subjected to Acute Moderate Exercise. Antioxidants (Basel) 2021 Jun 3;10(6).
    doi: 10.3390/antiox10060908pubmed: 34205129google scholar: lookup
  4. Long A, Nolen-Walston R. Equine Inflammatory Markers in the Twenty-First Century: A Focus on Serum Amyloid A. Vet Clin North Am Equine Pract 2020 Apr;36(1):147-160.
    doi: 10.1016/j.cveq.2019.12.005pubmed: 32007299google scholar: lookup
  5. Assunção P, Barbosa T, Yonezawa L, Barbosa L, Watanabe M, Kohayagawa A, Schmidt E. Acute-phase protein profile in horses subjected to different exercise protocols. Can J Vet Res 2019 Oct;83(4):272-278.
    pubmed: 31571727
  6. Leclere M, Lavoie-Lamoureux A, Lavoie JP. Acute phase proteins in racehorses with inflammatory airway disease. J Vet Intern Med 2015 May-Jun;29(3):940-5.
    doi: 10.1111/jvim.12587pubmed: 25857218google scholar: lookup
  7. Yaghoobpour T, Sheikhi Z, Nazifi S. The impact of stress in domestic animals: roles of heat shock proteins and acute-phase proteins. Vet Res Commun 2025 Jul 17;49(5):258.
    doi: 10.1007/s11259-025-10802-zpubmed: 40673978google scholar: lookup
  8. Kiełbik P, Witkowska-Piłaszewicz O. Iron Status in Sport Horses: Is It Important for Equine Athletes?. Int J Mol Sci 2025 Jun 12;26(12).
    doi: 10.3390/ijms26125653pubmed: 40565115google scholar: lookup
  9. Connysson M, Jansson A. Starch Allowance and Muscle Enzyme Activity in Healthy Standardbred Trotters Trained by Professional Trainers. J Anim Physiol Anim Nutr (Berl) 2025 Sep;109(5):1130-1137.
    doi: 10.1111/jpn.14127pubmed: 40329464google scholar: lookup
  10. Witkowska-Piłaszewicz O, Malin K, Dąbrowska I, Grzędzicka J, Ostaszewski P, Carter C. Immunology of Physical Exercise: Is Equus caballus an Appropriate Animal Model for Human Athletes?. Int J Mol Sci 2024 May 10;25(10).
    doi: 10.3390/ijms25105210pubmed: 38791248google scholar: lookup
  11. Giers J, Bartel A, Kirsch K, Müller SF, Horstmann S, Gehlen H. Blood-based assessment of oxidative stress, inflammation, endocrine and metabolic adaptations in eventing horses accounting for plasma volume shift after exercise. Vet Med Sci 2024 May;10(3):e1409.
    doi: 10.1002/vms3.1409pubmed: 38516822google scholar: lookup