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PloS one2024; 19(8); e0309474; doi: 10.1371/journal.pone.0309474

Social facilitation of trotting: Can horses perceive and adapt to the movement of another horse?

Abstract: Exercise intensity is prone to be self-regulated in horses exercising freely. The main drivers include social, feeding and escape behaviors, as well as the operant conditioning. We hypothesized that self-regulated exercise intensity may increase due to the presence of another horse exercising ahead. Seven horses were assigned to a 2x2 crossover trial following treadmill familiarization. Video images of a trotting horse were displayed on the wall in front of the experimental unit (Visual), which was positioned in the treadmill. Physiological and behavioral markers were further compared with a control visual stimulus (Co), comprising a racetrack image without horses. Horses were sampled during a constant load exercise test (1) at rest (baseline), (2) after the warm-up (0 - 10th minute) and (3) after visual stimulation or control (10th- 12th minutes of the SET) to quantify plasma lactate and glucose concentration, heart rate, head angle, as well as behavioral markers. Following visual stimulation, heart rate (130.8 ± 27.8 b.p.m.) was higher than control (84.7 ± 15.1 b.p.m., P = .017), as was plasma lactate (Visual - 5.28 ± 1.48 mg/dl; Co -3.27 ± 1.24 mg/dl, P = .042) and head angle (Visual - 36.43 ± 3.69°; Co -25.14 ± 4.88°, P = .003). The prevalence of "ears forward" behavior was also higher following Visual (100% - 7/7) than Co (14% - 1/7, P = .004). These results suggest that visual stimulus (1) was safe and well tolerated and (2) prompted the anaerobic lactic pathways and shifted the behavior to a vigilant state. In conclusion, horses were able to perceive and adapt to a social environment. Our findings validate the use of social facilitation of trotting to encourage horses to move forward avoiding the use of the whip.
Publication Date: 2024-08-26 PubMed ID: 39186726PubMed Central: PMC11346917DOI: 10.1371/journal.pone.0309474Google Scholar: Lookup
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  • Journal Article

Summary

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This research studies the effect of visual stimuli on the self-regulated exercise intensity of horses, particularly when displaying the image of another exercising horse, with findings suggesting that such stimuli could encourage horses to exert more, thus potentially eliminating the necessity of whips.

Research Method

  • The study involved seven horses which underwent a 2×2 crossover trial after being familiarized with a treadmill.
  • The experiment was initiated with a “Visual” treatment, where a video of a horse trotting was displayed in front of the experimental unit, placed on the treadmill.
  • This visual stimuli was then compared with a “Control” stimulus, comprising an image of a racetrack without any horses.
  • The horses were studied through a constant load exercise test during three stages: at rest (baseline), after the warm-up, and after either visual or control stimulation.

Data Collection and Results

  • Various physiological and behavioral markers were examined in each stage. These markers included plasma lactate and glucose concentration, heart rate, and the angle of the horse’s head, as well as behavioral markers.
  • The results revealed that the horses’ heart rate, plasma lactate, and head angle were significantly higher during the visual stimulation compared to the control.
  • The “ears forward” behavior, indicative of vigilance or arousal, was observed more frequently after visual stimulation.

Conclusions

  • The research suggests the visual stimulation was not only safe and well tolerated by horses, but it also more successful in inducing anaerobic lactic pathways which prompt higher physical exertion.
  • The horses exhibited changes in their behavior, indicating a shift to a more alert state due to the presence of an “other” in their perceived environment.
  • This study concludes that horses have the ability to perceive and adapt to a social environment, and that social facilitation of trotting could serve as a method to encourage physical exertion in horses without using a whip.

Cite This Article

APA
Bogossian PM, Pereira JS, da Silva NF, Hilgert AR, Seidel SRT, Fülber J, Belli CB, Fernandes WR. (2024). Social facilitation of trotting: Can horses perceive and adapt to the movement of another horse? PLoS One, 19(8), e0309474. https://doi.org/10.1371/journal.pone.0309474

Publication

ISSN: 1932-6203
NlmUniqueID: 101285081
Country: United States
Language: English
Volume: 19
Issue: 8
Pages: e0309474
PII: e0309474

Researcher Affiliations

Bogossian, Paulo Moreira
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.
Pereira, Juliana Santos
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.
da Silva, Nathalia Felicio
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.
Hilgert, Ayrton Rodrigo
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.
Seidel, Sarah Raphaela Torquato
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.
Fülber, Joice
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.
Belli, Carla Bargi
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.
Fernandes, Wilson Roberto
  • Department of Internal Medicine, University of Sao Paulo, School of Veterinary Medicine and Animal Science, São Paulo, Brazil.

MeSH Terms

  • Animals
  • Horses / physiology
  • Heart Rate / physiology
  • Physical Conditioning, Animal / physiology
  • Male
  • Behavior, Animal / physiology
  • Female
  • Lactic Acid / blood
  • Adaptation, Physiological / physiology
  • Blood Glucose
  • Cross-Over Studies
  • Movement / physiology
  • Exercise Test

Conflict of Interest Statement

The authors declare that there is no conflict of interest.

References

This article includes 38 references
  1. Norton K, Norton L, Sadgrove D. Position statement on physical activity and exercise intensity terminology.. Journal of Science and Medicine in Sport 2010;13(5):496–502.
    doi: 10.1016/j.jsams.2009.09.008pubmed: 20005170google scholar: lookup
  2. Guhl A, Lindner A, von Wittke P. Use of the relationship between blood lactate and running speed to determine the exercise intensity of horses.. Veterinary Record 1996;139(5):108–10.
    doi: 10.1136/vr.139.5.108pubmed: 8856887google scholar: lookup
  3. Robert C, Valette JP, Denoix JM. The effects of treadmill inclination and speed on the activity of two hindlimb muscles in the trotting horse.. Equine Vet J 2000;32(4):312–7.
    doi: 10.2746/042516400777032246pubmed: 10952380google scholar: lookup
  4. Bogossian PM, Di Filippo PA, Correia-Oliveira CR. Effect of racetrack surface on glycolytic activity of trained endurance horses.. International Journal of Performance Analysis in Sport 2021;21(1):12–21.
  5. Linklater WL, Cameron EZ, Minot EO, Stafford KJ. Stallion harassment and the mating system of horses.. Animal Behaviour 1999;58(2):295–306.
    doi: 10.1006/anbe.1999.1155pubmed: 10458881google scholar: lookup
  6. Eldridge DJ, Ding J, Travers SK. Feral horse activity reduces environmental quality in ecosystems globally.. Biological Conservation 2020;241:108367.
  7. McGreevy PD, Harman A, McLean A, Hawson L. Over-flexing the horse’s neck: A modern equestrian obsession?. Journal of Veterinary Behavior 2010;5(4):180–6.
  8. Evans D, McGreevy P. An Investigation of Racing Performance and Whip Use by Jockeys in Thoroughbred Races.. PLOS ONE 2011;6(1):e15622.
  9. Zajonc RB. Social Facilitation.. Science 1965;149(3681):269–74.
    doi: 10.1126/science.149.3681.269pubmed: 14300526google scholar: lookup
  10. van Meurs E, Greve J, Strauss B. Moving in the presence of others–a systematic review and meta-analysis on social facilitation.. International Review of Sport and Exercise Psychology 1-33.
  11. Harkins JD, Kamerling SG, Church G. Effect of competition on performance of thoroughbred racehorses.. Journal of Applied Physiology 1992;72(3):836–41.
    doi: 10.1152/jappl.1992.72.3.836pubmed: 1568979google scholar: lookup
  12. McLean AN, Christensen JW. The application of learning theory in horse training.. Applied Animal Behaviour Science 2017;190:18–27.
  13. Gueron S, Levin SA, Rubenstein DI. The Dynamics of Herds: From Individuals to Aggregations.. Journal of Theoretical Biology 1996;182(1):85–98.
    doi: 10.1006/jtbi.1996.0144google scholar: lookup
  14. Briard L, Dorn C, Petit O. Personality and Affinities Play a Key Role in the Organisation of Collective Movements in a Group of Domestic Horses.. Ethology 2015;121(9):888–902.
    doi: 10.1111/eth.12402google scholar: lookup
  15. Krapp HG. Sensorimotor transformation: from visual responses to motor commands.. Curr Biol 2010;20(5):R236–9.
    doi: 10.1016/j.cub.2010.01.024pubmed: 20219173google scholar: lookup
  16. Pouget A, Snyder LH. Computational approaches to sensorimotor transformations.. Nat Neurosci 2000;3 Suppl:1192–8.
    doi: 10.1038/81469pubmed: 11127837google scholar: lookup
  17. Card G, Dickinson MH. Visually mediated motor planning in the escape response of Drosophila.. Curr Biol 2008;18(17):1300–7.
    doi: 10.1016/j.cub.2008.07.094pubmed: 18760606google scholar: lookup
  18. Grasso FW. Invertebrate-Inspired sensory-motor systems and autonomous, olfactory-guided exploration.. Biol Bull 2001;200(2):160–8.
    doi: 10.2307/1543310pubmed: 11341578google scholar: lookup
  19. Hogg RC, Hodgins GA. Symbiosis or Sporting Tool? Competition and the Horse-Rider Relationship in Elite Equestrian Sports.. Animals (Basel) 2021;11(5).
    doi: 10.3390/ani11051352pmc: PMC8151029pubmed: 34068606google scholar: lookup
  20. Holmes TQ, Brown AF. Champing at the Bit for Improvements: A Review of Equine Welfare in Equestrian Sports in the United Kingdom.. Animals (Basel) 2022;12(9).
    doi: 10.3390/ani12091186pmc: PMC9100173pubmed: 35565612google scholar: lookup
  21. Pinchbeck GL, Clegg PD, Proudman CJ, Morgan KL, French NP. Whip use and race progress are associated with horse falls in hurdle and steeplechase racing in the UK.. Equine Veterinary Journal 2004;36(5):384–9.
    doi: 10.2746/0425164044868387pubmed: 15253077google scholar: lookup
  22. Wathan J, Burrows AM, Waller BM, McComb K. EquiFACS: The Equine Facial Action Coding System.. PLoS One 2015;10(8):e0131738.
  23. Hall CA, Cassaday HJ. An investigation into the effect of floor colour on the behaviour of the horse.. Applied Animal Behaviour Science 2006;99(3):301–14.
  24. Munsters CC, van Iwaarden A, van Weeren R, Sloet van Oldruitenborgh-Oosterbaan MM. Exercise testing in Warmblood sport horses under field conditions.. Vet J 2014;202(1):11–9.
    doi: 10.1016/j.tvjl.2014.07.019pubmed: 25172838google scholar: lookup
  25. Glancy B, Kane DA, Kavazis AN, Goodwin ML, Willis WT, Gladden LB. Mitochondrial lactate metabolism: history and implications for exercise and disease.. J Physiol 2021;599(3):863–88.
    doi: 10.1113/JP278930pmc: PMC8439166pubmed: 32358865google scholar: lookup
  26. Stomp M, Masson A, Henry S, Hausberger M, Lesimple C. Could snorts inform us on how horses perceive riding?. Behavioural Processes 2020;172:104041.
    doi: 10.1016/j.beproc.2020.104041pubmed: 31923434google scholar: lookup
  27. Estes Z, Verges M. Freeze or flee? Negative stimuli elicit selective responding.. Cognition 2008;108(2):557–65.
  28. Sankey C, Richard-Yris M-A, Henry S, Fureix C, Nassur F, Hausberger M. Reinforcement as a mediator of the perception of humans by horses (Equus caballus).. Animal Cognition 2010;13(5):753–64.
    doi: 10.1007/s10071-010-0326-9pubmed: 20490592google scholar: lookup
  29. Rochais C, Henry S, Hausberger M. Spontaneous attention-capture by auditory distractors as predictor of distractibility: a study of domestic horses (Equus caballus).. Scientific Reports 2017;7(1):15283.
    doi: 10.1038/s41598-017-15654-5pmc: PMC5681571pubmed: 29127367google scholar: lookup
  30. Beauchamp G. A comparative analysis of vigilance in birds.. Evolutionary Ecology 2010;24(5):1267–76.
    doi: 10.1007/s10682-010-9358-5google scholar: lookup
  31. HARMAN AM, MOORE S, HOSKINS R, KELLER P. Horse vision and an explanation for the visual behaviour originally explained by the ‘ramp retina’.. Equine Veterinary Journal 1999;31(5):384–90.
  32. Timney B, Keil K. Local and global stereopsis in the horse.. Vision Res 1999;39(10):1861–7.
    doi: 10.1016/s0042-6989(98)00276-4pubmed: 10343877google scholar: lookup
  33. CEHAK A, ROHN K, BARTON A-K, STADLER P, OHNESORGE B. EFFECT OF HEAD AND NECK POSITION ON PHARYNGEAL DIAMETER IN HORSES.. Veterinary Radiology & Ultrasound 2010;51(5):491–7.
  34. Lashley MJJO, Nauwelaerts S, Vernooij JCM, Back W, Clayton HM. Comparison of the head and neck position of elite dressage horses during top-level competitions in 1992 versus 2008.. The Veterinary Journal 2014;202(3):462–5.
    doi: 10.1016/j.tvjl.2014.08.028pubmed: 25296851google scholar: lookup
  35. Rorvang MV, Nielsen BL, McLean AN. Sensory Abilities of Horses and Their Importance for Equitation Science.. Front Vet Sci 2020;7:633.
    doi: 10.3389/fvets.2020.00633pmc: PMC7509108pubmed: 33033724google scholar: lookup
  36. Bartos L, Bartosová J, Starostová L. Position of the head is not associated with changes in horse vision.. Equine Vet J 2008;40(6):599–601.
    doi: 10.2746/042516408x332417pubmed: 19031516google scholar: lookup
  37. Range F, Horn L, Bugnyar T, Gajdon GK, Huber L. Social attention in keas, dogs, and human children.. Anim Cogn 2009;12(1):181–92.
    doi: 10.1007/s10071-008-0181-0pmc: PMC4415148pubmed: 18716802google scholar: lookup
  38. Tätte K, Ibáñez-Álamo JD, Markó G, Mänd R, Møller AP. Antipredator function of vigilance re-examined: vigilant birds delay escape.. Animal Behaviour 2019;156:97–110.

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