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Frontiers in pain research (Lausanne, Switzerland)2024; 5; 1463688; doi: 10.3389/fpain.2024.1463688

Investigating conditioned pain modulation in horses: can the lip-twitch be used as a conditioning stimulus?

Abstract: Study objective was to evaluate whether the application of a lip twitch could be proposed as conditioning stimulus in the context of a novel Conditioned Pain Modulation (CPM) assessment paradigm for use in horses. The study was a prospective, experimental, randomized trial. Twelve healthy horses were evaluated in two experimental sessions. The lip twitch was used as the conditioning stimulus in both sessions; electrical stimulation was used as the test stimulus in one session, while mechanical and thermal stimulations were used in the other. Differences between thresholds recorded before and during twitching (Δ) as well as their percent (%) change were computed for each stimulation modality as a measure of CPM. Heart rate and respiratory rate were recorded throughout the experiments to monitor physiological reactions, while the general level of stress and aversiveness toward twitching were scored using behavioural scales. Based on these scores, interruption criteria were defined. Ten and seven horses completed the electrical and mechanical/thermal experimental sessions respectively. For electrical stimulation, median (IQR) Δ was -2.8 (-3.9, -1.1) mA and% change 87.9 (65.7-118.2)%; for mechanical stimulation, Δ was -18.2 (-6.4, -21.4) N and% change 343.5 (140, 365.3)%; for thermal stimulation, Δ was -3.1 (-9.2, -2.1)°C, while% change was not calculated. Heart rate and respiratory rates varied significantly over time, with higher values recorded during twitching. Median stress and aversion scores did not differ between the two sessions. As lip twitching consistently affected thresholds to all stimulation modalities, it can be proposed as effective conditioning method for CPM assessment in horses. The exclusion of subjects due to severe aversion shows that this paradigm cannot be indistinctively applied to all horses and that stringent interruption criteria are necessary to guarantee adequate welfare during testing.
Publication Date: 2024-10-24 PubMed ID: 39512387PubMed Central: PMC11540819DOI: 10.3389/fpain.2024.1463688Google Scholar: Lookup
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  • Journal Article

Summary

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This research article explores the use of a lip twitch as a conditioning stimulus in a Conditioned Pain Modulation (CPM) assessment for horses. The findings suggest that lip twitching can effectively influence thresholds for various stimulation types, thereby demonstrating its potential use as a conditioning method for CPM assessment. However, the method may not suit all horses, necessitating stringent testing guidelines to ensure their welfare.

Research Methodology

  • The research was designed as a prospective, experimental, randomized trial involving twelve healthy horses.
  • Each horse participated in two experimental sessions, during both of which the lip twitch was applied as the conditioning stimulus. Different test stimuli were employed for each session, including electrical stimulation in the first and mechanical and thermal stimulations in the second.
  • Experiments were carried out while keeping close monitoring of the horses’ heart and respiratory rates. The researchers also scored each horse’s level of stress and resistance to the lip twitch using special behavioural scales.

Data Collection and Analysis

  • Change in thresholds recorded before and during twitching and change in percentages was calculated for each stimulation modality as a measure of CPM.
  • Heart rate and respiratory rate changes over time, particularly during the lip twitch, were also recorded.
  • Behaviours were scored for stress and aversion to determine the level of tolerance each horse had to the lip twitch application.
  • Based on these data, certain breaking criteria were established to determine when to discontinue the test for a particular horse.

Results and Findings

  • The majority of horses completed both experimental sessions. Results showed consistent alteration in thresholds to all stimulation modalities when the lip twitch was in use.
  • Both heart and respiratory rates significantly increased during the twitching session.
  • The median stress and aversion scores, however, remained relatively consistent across both sessions.
  • While the lip twitch can be suggested as an effective conditioning method for CPM assessments in horses, it’s essential to monitor signs of severe aversion and stress from the animal and apply stringent interruption criteria to ensure welfare during testing.

Cite This Article

APA
Blum S, Gisler J, Dalla Costa E, Montavon S, Spadavecchia C. (2024). Investigating conditioned pain modulation in horses: can the lip-twitch be used as a conditioning stimulus? Front Pain Res (Lausanne), 5, 1463688. https://doi.org/10.3389/fpain.2024.1463688

Publication

ISSN: 2673-561X
NlmUniqueID: 9918227269806676
Country: Switzerland
Language: English
Volume: 5
Pages: 1463688
PII: 1463688

Researcher Affiliations

Blum, Severin
  • Anaesthesiology and Pain Therapy Section, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
  • Veterinary Department of the Swiss Armed Forces, Bern, Switzerland.
Gisler, Jana
  • Anaesthesiology and Pain Therapy Section, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
  • Veterinary Department of the Swiss Armed Forces, Bern, Switzerland.
Dalla Costa, Emanuela
  • Department of Veterinary Medicine and Animal Sciences, University of Milan, Lodi, Italy.
Montavon, Stéphane
  • Veterinary Department of the Swiss Armed Forces, Bern, Switzerland.
Spadavecchia, Claudia
  • Anaesthesiology and Pain Therapy Section, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

This article includes 42 references
  1. Auer U, Kelemen Z, Vogl C, von Ritgen S, Haddad R, Torres Borda L. Development, refinement, and validation of an equine musculoskeletal pain scale. Front Pain Res (Lausanne) (2024) 4:2.
    doi: 10.3389/fpain.2023.1292299pmc: PMC10837853pubmed: 38312997google scholar: lookup
  2. Dyson S, Berger J, Ellis AD, Mullard J. Development of an ethogram for a pain scoring system in ridden horses and its application to determine the presence of musculoskeletal pain. J Vet Behav (2018) 23:47–57.
  3. Muir WW. Pain: mechanisms and management in horses. Vet Clin North Am Equine Pract (2010) 26(3):467–80.
    doi: 10.1016/j.cveq.2010.07.008pubmed: 21056294google scholar: lookup
  4. Al Naem M, Litzke LF, Failing K, Burk J, Rocken M. Hoof kinetic patterns differ between sound and laminitic horses. Equine Vet J (2021) 53(3):503–9.
    doi: 10.1111/evj.13311pubmed: 32542795google scholar: lookup
  5. Lawin FJ, Bystrom A, Roepstorff C, Rhodin M, Almlof M, Silva M. Is markerless more or less? Comparing a smartphone computer vision method for equine lameness assessment to multi-camera motion capture. Animals (Basel) (2023) 13(3):1–44.
    doi: 10.3390/ani13030390pmc: PMC9913208pubmed: 36766279google scholar: lookup
  6. Phutthachalee S, Mahlmann K, Seesupa S, Lischer C. Upper body movement analysis of multiple limb asymmetry in 367 clinically lame horses. Equine Vet J (2021) 53(4):701–9.
    doi: 10.1111/evj.13367pubmed: 33031613google scholar: lookup
  7. Costa E D, Stucke D, Dai F, Minero M, Leach MC, Lebelt D. Using the horse grimace scale (HGS) to assess pain associated with acute laminitis in horses (equus caballus). Animals (Basel) (2016) 6(8):1–9.
    doi: 10.3390/ani6080047pmc: PMC4997272pubmed: 27527224google scholar: lookup
  8. Torcivia C, McDonnell S. Equine discomfort ethogram. Animals (Basel) (2021) 11(2):1–21.
    doi: 10.3390/ani11020580pmc: PMC7931104pubmed: 33672338google scholar: lookup
  9. van Loon J, Macri L. Objective assessment of chronic pain in horses using the horse chronic pain scale (HCPS): a scale-construction study. Animals (Basel) (2021) 11(6):1–11.
    doi: 10.3390/ani11061826pmc: PMC8234780pubmed: 34207290google scholar: lookup
  10. Haussler KK. Pressure algometry for the detection of mechanical nociceptive thresholds in horses. Animals (Basel) (2020) 10(12):1–22.
    doi: 10.3390/ani10122195pmc: PMC7760268pubmed: 33255216google scholar: lookup
  11. Pujol R, Girard CA, Richard H, Hassanpour I, Binette MP, Beauchamp G. Synovial nerve fiber density decreases with naturally-occurring osteoarthritis in horses. Osteoarthritis Cartilage (2018) 26(10):1379–88.
    doi: 10.1016/j.joca.2018.06.006pubmed: 29958917google scholar: lookup
  12. Ramaswamy S, Wodehouse T. Conditioned pain modulation-A comprehensive review. Neurophysiol Clin (2021) 51(3):197–208.
    doi: 10.1016/j.neucli.2020.11.002pubmed: 33334645google scholar: lookup
  13. Lewis GN, Heales L, Rice DA, Rome K, McNair PJ. Reliability of the conditioned pain modulation paradigm to assess endogenous inhibitory pain pathways. Pain Res Manag (2012) 17(2):98–102.
    doi: 10.1155/2012/610561pmc: PMC3393056pubmed: 22518372google scholar: lookup
  14. Yarnitsky D. Role of endogenous pain modulation in chronic pain mechanisms and treatment. Pain (2015) 156(Suppl 1):S24–31.
  15. Young T, Creighton E, Smith T, Hosie C. A novel scale of behavioural indicators of stress for use with domestic horses. Appl Anim Behav Sci (2012) 140(1–2):33–43.
  16. Schambourg M, Taylor PM. Mechanical nociceptive thresholds in endurance horses. Vet Rec (2020) 186(4):2.
    doi: 10.1136/vr.105499pubmed: 31563891google scholar: lookup
  17. Yarnitsky D, Arendt-Nielsen L, Bouhassira D, Edwards RR, Fillingim RB, Granot M. Recommendations on terminology and practice of psychophysical DNIC testing. Eur J Pain (2010) 14(4):339.
    doi: 10.1016/j.ejpain.2010.02.004pubmed: 20227310google scholar: lookup
  18. Knych HK, Stucker K, Gretler SR, Kass PH, McKemie DS. Pharmacokinetics, adverse effects and effects on thermal nociception following administration of three doses of codeine to horses. BMC Vet Res (2022) 18(1):196.
    doi: 10.1186/s12917-022-03299-0pmc: PMC9131543pubmed: 35614473google scholar: lookup
  19. Love EJ, Taylor PM, Murrell J, Whay HR. Effects of acepromazine, butorphanol and buprenorphine on thermal and mechanical nociceptive thresholds in horses. Equine Vet J (2012) 44(2):221–5.
  20. Schelp D. Untersuchungen Ethologischer und Physiologischer Parameter zur Wirkungsweise und Möglichen Tierschutzrelevanz der Nasenbremse Beim Pferd. Stuttgart: Ludwig-Maximilians-Universität München; (2000).
  21. Lagerweij E, Nelis PC, Wiegant VM, Vanree JM. The twitch in horses - a variant of acupuncture. Science (1984) 225(4667):1172–4.
    doi: 10.1126/science.6089344pubmed: 6089344google scholar: lookup
  22. Vreeman H. The Effectiveness of the Twitch in Donkeys. Utrecht: Utrecht University; (2009).
  23. Mccarthy RN, Jeffcott LB, Clarke IJ. Preliminary studies on the use of plasma Beta-endorphin in horses as an indicator of stress and pain. J Equine Vet Sci (1993) 13(4):216–9.
  24. Aparecida da Silva V, Galhardoni R, Teixeira MJ, Ciampi de Andrade D. Not just a matter of pain intensity: effects of three different conditioning stimuli on conditioned pain modulation effects. Neurophysiol Clin (2018) 48(5):287–93.
    doi: 10.1016/j.neucli.2018.06.078pubmed: 29954673google scholar: lookup
  25. Oono Y, Nie H, Matos RL, Wang K, Arendt-Nielsen L. The inter- and intra-individual variance in descending pain modulation evoked by different conditioning stimuli in healthy men. Scand J Pain (2011) 2(4):162–9.
    doi: 10.1016/j.sjpain.2011.05.006pubmed: 29913755google scholar: lookup
  26. Kennedy DL, Kemp HI, Ridout D, Yarnitsky D, Rice ASC. Reliability of conditioned pain modulation: a systematic review. Pain (2016) 157(11):2410–9.
  27. Casoni D, Mirra A, Suter MR, Gutzwiller A, Spadavecchia C. Can disbudding of calves (one versus four weeks of age) induce chronic pain?. Physiol Behav (2019) 199:47–55.
    doi: 10.1016/j.physbeh.2018.11.010pubmed: 30414886google scholar: lookup
  28. Chiu KW, Hash J, Meyers R, Lascelles BDX. The effect of spontaneous osteoarthritis on conditioned pain modulation in the canine model. Sci Rep (2020) 10(1):1694.
    doi: 10.1038/s41598-020-58499-1pmc: PMC6997173pubmed: 32015421google scholar: lookup
  29. Willer JC, Roby A, Le Bars D. Psychophysical and electrophysiological approaches to the pain-relieving effects of heterotopic nociceptive stimuli. Brain (1984) 107(Pt 4):1095–112.
    doi: 10.1093/brain/107.4.1095pubmed: 6509310google scholar: lookup
  30. Moont R, Pud D, Sprecher E, Sharvit G, Yarnitsky D. ‘Pain inhibits pain’ mechanisms: is pain modulation simply due to distraction?. Pain (2010) 150(1):113–20.
    doi: 10.1016/j.pain.2010.04.009pubmed: 20493631google scholar: lookup
  31. Yarnitsky D, Bouhassira D, Drewes AM, Fillingim RB, Granot M, Hansson P. Recommendations on practice of conditioned pain modulation (CPM) testing. Eur J Pain (2015) 19(6):805–6.
    doi: 10.1002/ejp.605pubmed: 25330039google scholar: lookup
  32. Biurrun Manresa JA, Fritsche R, Vuilleumier PH, Oehler C, Morch CD, Arendt-Nielsen L. Is the conditioned pain modulation paradigm reliable? A test-retest assessment using the nociceptive withdrawal reflex. PLoS One (2014) 9(6):e100241.
  33. Schliessbach J, Lutolf C, Streitberger K, Scaramozzino P, Arendt-Nielsen L, Curatolo M. Reference values of conditioned pain modulation. Scand J Pain (2019) 19(2):279–86.
    doi: 10.1515/sjpain-2018-0356pubmed: 30699074google scholar: lookup
  34. Flakoll B, Ali AB, Saab CY. Twitching in veterinary procedures: how does this technique subdue horses?. J Vet Behav (2016) 18:23–8.
  35. Ferlazzo A, Fazio E, Cravana C, Medica P. The role of circulating β-endorphin in different stress models in equines: a review. J Equine Vet Sci (2018) 71:98–104.
  36. Golynski M, Krumrych W, Lutnicki K. The role of beta-endorphin in horses: a review. Vet Med (Praha) (2011) 56(9):423–9.
    doi: 10.17221/3205-VETMEDgoogle scholar: lookup
  37. Ali ABA, Gutwein KL, Heleski CR. Assessing the influence of upper lip twitching in naive horses during an aversive husbandry procedure (ear clipping). J Vet Behav (2017) 21:20–5.
  38. Matsui K, Sugano S, Amada A. Heart rate and ECG response to twitching in thoroughbred foals and mares. JpnJVetSci (1986) 48(2):305–12.
    doi: 10.1292/jvms1939.48.305pubmed: 3712891google scholar: lookup
  39. Ferlazzo A, Cravana C, Fazio E, Medica P. The different hormonal system during exercise stress coping in horses. Vet World (2020) 13(5):847–59.
  40. Harvey MP, Dubois MC, Chalaye P, Sansoucy Y, Marchand S. Sex-related effects of adrenergic drugs on conditioned pain modulation: a randomized controlled cross-over double-blind trial. Pain Res Manag (2022) 2022:2757101.
    doi: 10.1155/2022/2757101pmc: PMC9629924pubmed: 36339068google scholar: lookup
  41. Forkman B, Boissy A, Meunier-Salaun MC, Canali E, Jones RB. A critical review of fear tests used on cattle, pigs, sheep, poultry and horses. Physiol Behav (2007) 92(3):340–74.
    doi: 10.1016/j.physbeh.2007.03.016pubmed: 18046784google scholar: lookup
  42. McGreevy PD, McLean AN. Punishment in horse-training and the concept of ethical equitation. J Vet Behav (2009) 4(5):193–7.

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