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Animals : an open access journal from MDPI2025; 15(15); 2259; doi: 10.3390/ani15152259

Motion Coupling at the Cervical Vertebral Joints in the Horse-An Ex Vivo Study Using Bone-Anchored Markers.

Abstract: The influence of soft tissue structures, including ligaments spanning one or more intervertebral junctions and the nuchal ligament, on motion of the equine cervical joints remains unclear. The present study addressed this using four post-mortem horse specimens extending from head to withers with all ligaments intact. Three-dimensional kinematics was obtained from markers on the head and bone-anchored markers on each cervical and the first thoracic vertebra during rotation, lateral bending, flexion and extension of the whole head, and neck segment. Yaw, pitch, and roll angles in 8 cervical joints (total 32) were calculated. Flexion and extension were expressed mainly as pitch in 27 and 22 joints, respectively. Rotation appeared as predominantly roll in 13 joints, whereas lateral bending was represented as predominantly yaw in 1 and as roll or pitch in all other joints. Significant correlations between yaw, pitch, and roll were observed at individual cervical joints in 97% of all measurements, with the atlanto-occipital joint showing complete (100%) correlation. Most non-significant correlations occurred at the C5-C6 joint, while C6-C7 exhibited significantly lower correlation coefficients compared to other levels. The overall movement of the head and neck is not replicated at individual cervical joint levels and should be considered when evaluating equine necks in vivo.
Publication Date: 2025-08-01 PubMed ID: 40805049PubMed Central: PMC12345553DOI: 10.3390/ani15152259Google Scholar: Lookup
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  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research is focused on investigating the nature of motion in horse’s cervical (neck) joints and its relationship with various soft tissues, using post-mortem specimens. The study used bone-anchored markers to identify patterns in rotation, bending, flexion and extension of the neck and head, measured in yaw, pitch, and roll.

Methodology

  • The researchers conducted an ex vivo study using four post-mortem horse specimens with intact ligaments and other soft tissue structures. The specimens consisted of the head, neck, and the first portion of the torso, called the withers.
  • Bone-anchored markers were placed on the head and each cervical vertebrae up to the first thoracic vertebra of the horse’s spine. This allowed tracking and recording of three-dimensional movement.
  • The entire head and neck segment of the specimens were subjected to various movements such as rotation, lateral bending, flexion and extension. The objective here was to measure and characterize how these movements are expressed and interact at each individual vertebral joint.

Findings

  • Finding patterns in movements, the researchers were able to measure the yaw, pitch and roll angles in eight cervical joints under different movements. For instance, flexion and extension mainly resulted in changes to pitch in 27 and 22 joints respectively, whereas rotation was predominantly roll in 13 joints.
  • Lateral bending was mainly represented as yaw in one instance, but otherwise resulted in roll or pitch in all joints. This shows the complexity of movement at each vertebral joint.
  • Strong correlations were detected between yaw, pitch and roll at individual cervical joints, accounting for 97% of all measurements. The joint between the head and first cervical vertebra (atlanto-occipital joint) showed a complete correlation.
  • Some joints, however, did not follow this pattern. Most non-significant correlations were found at the joint between the 5th and 6th vertebrae, while the joint between the 6th and 7th vertebrae had noticeably lower correlation coefficients compared to other levels.

Implications

  • The findings from this study shed light on the complex movements occurring in the cervical joints of a horse. The influence of soft tissue structures on these movements was also noted, although the specifics of this influence remain unclear.
  • The detected variations in movement and correlations between cervical joints indicate that overall head and neck movement is not directly mirrored at individual cervical joint levels.
  • These insights into equine cervical joint motion and its variation across joints should be considered in live examination and treatment approaches for horses, as they indicate that a comprehensive understanding of movements at each vertebral joint level is required for accurate diagnosis and intervention.

Cite This Article

APA
Bosch K, Zsoldos RR, Hartig A, Licka T. (2025). Motion Coupling at the Cervical Vertebral Joints in the Horse-An Ex Vivo Study Using Bone-Anchored Markers. Animals (Basel), 15(15), 2259. https://doi.org/10.3390/ani15152259

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 15
Issue: 15
PII: 2259

Researcher Affiliations

Bosch, Katharina
  • Clinical Department for Small Animals and Horses, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Zsoldos, Rebeka R
  • Department of Biosystems and Technology, Swedish University of Agricultural Sciences, 23422 Alnarp, Sweden.
  • School of Agriculture and Food Sustainability, The University of Queensland, Gatton, QLD 4343, Australia.
Hartig, Astrid
  • Clinical Department for Small Animals and Horses, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Licka, Theresia
  • Clinical Department for Small Animals and Horses, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
  • Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh EH8 9YL, UK.

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 54 references
  1. Zsoldos RR, Licka TF. The Equine Neck and Its Function during Movement and Locomotion. Zoology 2015;118:364–376.
    doi: 10.1016/j.zool.2015.03.005pubmed: 26163862google scholar: lookup
  2. Galis F. Why Do Almost All Mammals Have Seven Cervical Vertebrae? Developmental Constraints, Hox Genes, and Cancer. J. Exp. Zool. 1999;285:19–26.
  3. Dyson S, Murray R. Equine Neck and Back Pathology: Diagnosis and Treatment. Elsevier; Edinburgh, UK: 2018. Vertebral Column; pp. 60–78.
  4. Nickel R, Schummer A, Seiferle E. Lehrbuch der Anatomie der Haustiere. Volume 1. Parey; Stuttgart, Germany: 2004. Skelett Des Stammes, Wirbelsäule- Columna Vertebralis; pp. 30–38, 59, 221–228.
  5. König HE, Liebig H-G. Anatomie der Haussäugetiere. Schattauer; Stuttgart, Germany: 2005. Skelett Des Stammes; pp. 82–88.
  6. Buchner HHF, Savelberg HHCM, Schamhardt HC, Barneveld A. Inertial Properties of Dutch Warmblood Horses. J. Biomech. 1997;30:653–658.
    doi: 10.1016/S0021-9290(97)00005-5pubmed: 9165402google scholar: lookup
  7. Moore J. General Biomechanics: The Horse As a Biological Machine. J. Equine Vet. Sci. 2010;30:379–383.
  8. Zsoldos RR, Krüger B, Licka TF. From Maturity to Old Age: Tasks of Daily Life Require a Different Muscle Use in Horses. Comp. Exerc. Physiol. 2014;10:75–88.
    doi: 10.3920/CEP140001pmc: PMC5495164pubmed: 28680481google scholar: lookup
  9. Hepburn R. Equine Neurology. John Wiley & Sons, Ltd.; Hoboken, NJ, USA: 2015. Cervical Articular Process Disease, Fractures, and Other Axial Skeletal Disorders; pp. 386–400.
  10. Story MR, Haussler KK, Nout-Lomas YS, Aboellail TA, Kawcak CE, Barrett MF, Frisbie DD, McIlwraith CW. Equine Cervical Pain and Dysfunction: Pathology, Diagnosis and Treatment. Animals 2021;11:422.
    doi: 10.3390/ani11020422pmc: PMC7915466pubmed: 33562089google scholar: lookup
  11. Harrison LM, Sole-Guitart A, Ahern B, Goff LM. Functional Anatomy of the Equine Thoracolumbar Spine Related to Equine Back Rehabilitation. J. Equine Rehabil. 2025;3:100027.
  12. Ehrle A, Ressel L, Ricci E, Singer ER. Structure and Innervation of the Equine Supraspinous and Interspinous Ligaments. Anat. Histol. Embryol. 2017;46:223–231.
    doi: 10.1111/ahe.12261pubmed: 28122400google scholar: lookup
  13. May-Davis S, Kleine J. Variations and Implications of the Gross Anatomy in the Equine Nuchal Ligament Lamellae. J. Equine Vet. Sci. 2014;34:1110–1113.
  14. Gellman KS, Bertram JEA. The Equine Nuchal Ligament 1: Structural and Material Properties. Vet. Comp. Orthop. Traumatol. 2002;15:1–6.
    doi: 10.1055/s-0038-1632705google scholar: lookup
  15. Clayton HM, Hobbs S-J. The Role of Biomechanical Analysis of Horse and Rider in Equitation Science. Appl. Anim. Behav. Sci. 2017;190:123–132.
  16. Krings M, Nyakatura JA, Boumans MLLM, Fischer MS, Wagner H. Barn Owls Maximize Head Rotations by a Combination of Yawing and Rolling in Functionally Diverse Regions of the Neck. J. Anat. 2017;231:12–22.
    doi: 10.1111/joa.12616pmc: PMC5472525pubmed: 28449202google scholar: lookup
  17. Neto ENA, Barreto RM, Duarte RM, Magalhaes JP, Bastos CACM, Ren TI, Cavalcanti GDC. Real-Time Head Pose Estimation for Mobile Devices. In: Yin H., Costa J.A.F., Barreto G., editors. Intelligent Data Engineering and Automated Learning—IDEAL 2012. Volume 7435. Springer; Berlin/Heidelberg, Germany: 2012. pp. 467–474. (Lecture Notes in Computer Science).
  18. Ishii T, Mukai Y, Hosono N, Sakaura H, Fujii R, Nakajima Y, Tamura S, Iwasaki M, Yoshikawa H, Sugamoto K. Kinematics of the Cervical Spine in Lateral Bending: In Vivo Three-Dimensional Analysis. Spine 2006;31:155–160.
  19. Ishii T, Mukai Y, Hosono N, Sakaura H, Nakajima Y, Sato Y, Sugamoto K, Yoshikawa H. Kinematics of the Upper Cervical Spine in Rotation: In Vivo Three-Dimensional Analysis. Spine 2004;29:E139–E144.
  20. Panjabi MM, Crisco JJ, Vasavada A, Oda T, Cholewicki J, Nibu K, Shin E. Mechanical Properties of the Human Cervical Spine as Shown by Three-Dimensional Load–Displacement Curves. Spine 2001;26:2692–2700.
  21. Merten LJF, Manafzadeh AR, Herbst EC, Amson E, Tambusso PS, Arnold P, Nyakatura JA. The Functional Significance of Aberrant Cervical Counts in Sloths: Insights from Automated Exhaustive Analysis of Cervical Range of Motion. Proc. R. Soc. B 2023;290:20231592.
    doi: 10.1098/rspb.2023.1592pmc: PMC10618861pubmed: 37909076google scholar: lookup
  22. Clayton HM, Townsend HGG. Kinematics of the Cervical Spine of the Adult Horse. Equine Vet. J. 1989;21:189–192.
  23. Schulze N, Ehrle A, Weller R, Fritsch G, Gernhardt J, Ben Romdhane R, Lischer C. Computed Tomographic Evaluation of Adjacent Segment Motion after Ex Vivo Fusion of Equine Third and Fourth Cervical Vertebrae. Vet. Comp. Orthop. Traumatol. 2020;33:001–008.
    doi: 10.1055/s-0039-1693665pubmed: 31387122google scholar: lookup
  24. Schmidburg I, Pagger H, Zsoldos RR, Mehnen J, Peham C, Licka TF. Movement Associated Reduction of Spatial Capacity of the Equine Cervical Vertebral Canal. Vet. J. 2012;192:525–528.
    doi: 10.1016/j.tvjl.2011.08.011pubmed: 21920786google scholar: lookup
  25. Pagger H, Schmidburg I, Peham C, Licka T. Determination of the Stiffness of the Equine Cervical Spine. Vet. J. 2010;186:338–341.
    doi: 10.1016/j.tvjl.2009.09.015pubmed: 19850500google scholar: lookup
  26. Clayton HM, Kaiser LJ, Lavagnino M, Stubbs NC. Evaluation of Intersegmental Vertebral Motion during Performance of Dynamic Mobilization Exercises in Cervical Lateral Bending in Horses. Am. J. Veter-Res. 2012;73:1153–1159.
    doi: 10.2460/ajvr.73.8.1153pubmed: 22849675google scholar: lookup
  27. Zsoldos RR, Groesel M, Kotschwar A, Kotschwar AB, Licka T, Peham C. A Preliminary Modelling Study on the Equine Cervical Spine with Inverse Kinematics at Walk. Equine Vet. J. 2010;42:516–522.
  28. Latash ML. The Bliss (Not the Problem) of Motor Abundance (Not Redundancy). Exp. Brain. Res. 2012;217:1–5.
    doi: 10.1007/s00221-012-3000-4pmc: PMC3532046pubmed: 22246105google scholar: lookup
  29. Nakano N, Iino Y, Inaba Y, Fukashiro S, Yoshioka S. Utilizing Hierarchical Redundancy for Accurate Throwing Movement. Hum. Mov. Sci. 2022;81:102918.
    doi: 10.1016/j.humov.2021.102918pubmed: 34968877google scholar: lookup
  30. Singh P, Jana S, Ghosal A, Murthy A. Exploration of Joint Redundancy but Not Task Space Variability Facilitates Supervised Motor Learning. Proc. Natl. Acad. Sci. USA 2016;113:14414–14419.
    doi: 10.1073/pnas.1613383113pmc: PMC5167208pubmed: 27911808google scholar: lookup
  31. Edelman GM, Gally JA. Degeneracy and Complexity in Biological Systems. Proc. Natl. Acad. Sci. USA 2001;98:13763–13768.
    doi: 10.1073/pnas.231499798pmc: PMC61115pubmed: 11698650google scholar: lookup
  32. Papi E, Bull AMJ, McGregor AH. Spinal Segments Do Not Move Together Predictably during Daily Activities. Gait Posture 2019;67:277–283.
  33. Egenvall A, Engström H, Byström A. Back Motion in Unridden Horses in Walk, Trot and Canter on a Circle. Vet. Res. Commun. 2023;47:1831–1843.
    doi: 10.1007/s11259-023-10132-ypmc: PMC10698108pubmed: 37127806google scholar: lookup
  34. Von Borstel U, Kienapfel K, McLean A, Wilkins C, McGreevy P. Hyperflexing the Horse’s Neck: A Systematic Review and Meta-Analysis. Sci. Rep. 2024;14:22886.
    doi: 10.1038/s41598-024-72766-5pmc: PMC11446961pubmed: 39358404google scholar: lookup
  35. Rhodin M, Johnston C, Holm KR, Wennerstrand J, Drevemo S. The Influence of Head and Neck Position on Kinematics of the Back in Riding Horses at the Walk and Trot. Equine Vet. J. 2005;37:7–11.
    doi: 10.2746/0425164054406928pubmed: 15651727google scholar: lookup
  36. Johnson JA, Da Costa RC, Bhattacharya S, Goel V, Allen MJ. Kinematic Motion Patterns of the Cranial and Caudal Canine Cervical Spine. Vet. Surg. 2011;40:720–727.
  37. Goel A, Shah A, Kothari M, Gaikwad S, Dhande P. Comparative Quantitative Analysis of Osseous Anatomy of the Craniovertebral Junction of Tiger, Horse, Deer, and Humans. J. Craniovert. Jun. Spine. 2011;2:32.
    doi: 10.4103/0974-8237.85311pmc: PMC3190428pubmed: 22013373google scholar: lookup
  38. Mayhew IG, Watson AG, Heissan JA. Congenital Occipitoatlantoaxial Malformations in the Horse. Equine Vet. J. 1978;10:103–113.
  39. Licka T. Closed Reduction of an Atlanto-occipital and Atlantoaxial Dislocation in a Foal. Vet. Rec. 2002;151:356–357.
    doi: 10.1136/vr.151.12.356pubmed: 12371694google scholar: lookup
  40. Puangthong C, Bootcha R, Petchdee S, Chanda M. Chronic Atlantoaxial Luxation Imaging Features in a Pony with Intermittent Neck Stiffness. J. Equine Vet. Sci. 2020;91:103128.
    doi: 10.1016/j.jevs.2020.103128pubmed: 32684266google scholar: lookup
  41. Zhou C, Wang H, Wang C, Tsai T-Y, Yu Y, Ostergaard P, Li G, Cha T. Intervertebral Range of Motion Characteristics of Normal Cervical Spinal Segments (C0-T1) during in Vivo Neck Motions. J. Biomech. 2020;98:109418.
  42. Cook C, Hegedus E, Showalter C, Sizer PS. Coupling Behavior of the Cervical Spine: A Systematic Review of the Literature. J. Manip. Physiol. Ther. 2006;29:570–575.
    doi: 10.1016/j.jmpt.2006.06.020pubmed: 16949947google scholar: lookup
  43. Panjabi MM, Summers DJ, Pelker RR, Videman T, Friedlaender GE, Southwick WO. Three-dimensional Load-displacement Curves Due to Forces on the Cervical Spine. J. Orthop. Res. 1986;4:152–161.
    doi: 10.1002/jor.1100040203pubmed: 3712124google scholar: lookup
  44. Anderst WJ, Donaldson WF, Lee JY, Kang JD. Cervical Motion Segment Percent Contributions to Flexion-Extension During Continuous Functional Movement in Control Subjects and Arthrodesis Patients. Spine 2013;38:E533–E539.
  45. Reardon RJM, Bailey R, Walmsley JP, Heller J, Lischer C. An In Vitro Biomechanical Comparison of a Locking Compression Plate Fixation and Kerf Cut Cylinder Fixation for Ventral Arthrodesis of the Fourth and the Fifth Equine Cervical Vertebrae: Ventral Arthrodesis of Equine Cervical Vertebrae. Vet. Surg. 2010;39:980–990.
  46. Baudisch N, Schneidewind L, Becke S, Keller M, Overhoff M, Tettke D, Gruben V, Eichler F, Meyer HJ, Lischer C. Computed Tomographic Study Analysing Functional Biomechanics in the Thoracolumbar Spine of Horses with and without Spinal Pathology. Anat. Histol. Embryol. 2024;53:e13016.
    doi: 10.1111/ahe.13016pubmed: 38230834google scholar: lookup
  47. Nestadt CL, Lusi CM, Davies HMS. Effect of Different Head-and-Neck Positions on Nuchal Ligament Dimensions in Fetal Foals. J. Equine Vet. Sci. 2015;35:153–160.
  48. Dippel M, Zsoldos RR, Licka TF. An Equine Cadaver Study Investigating the Relationship between Cervical Flexion, Nuchal Ligament Elongation and Pressure at the First and Second Cervical Vertebra. Vet. J. 2019;252:105353.
    doi: 10.1016/j.tvjl.2019.105353pubmed: 31554589google scholar: lookup
  49. Valentin S, Grösel M, Licka T. The Presence of Long Spinal Muscles Increases Stiffness and Hysteresis of the Caprine Spine In-Vitro. J. Biomech. 2012;45:2506–2512.
  50. Jung H, Vangipuram G, Fisher MB, Yang G, Hsu S, Bianchi J, Ronholdt C, Woo SL. The Effects of Multiple Freeze–Thaw Cycles on the Biomechanical Properties of the Human Bone-patellar Tendon-bone Allograft. J. Orthop. Res. 2011;29:1193–1198.
    doi: 10.1002/jor.21373pmc: PMC3132590pubmed: 21374710google scholar: lookup
  51. Moon DK, Woo SL-Y, Takakura Y, Gabriel MT, Abramowitch SD. The Effects of Refreezing on the Viscoelastic and Tensile Properties of Ligaments. J. Biomech. 2006;39:1153–1157.
  52. Panjabi MM, Krag M, Summers D, Videman T. Biomechanical Time-tolerance of Fresh Cadaveric Human Spine Specimens. J. Orthop. Res. 1985;3:292–300.
    doi: 10.1002/jor.1100030305pubmed: 4032102google scholar: lookup
  53. Nickel R, Schummer A, Seiferle E. Lehrbuch der Anatomie der Haustiere. Volume 1. Parey; Stuttgart, Germany: 2004. Muskeln Des Stammes; pp. 333–403.
  54. König HE, Liebich H-G. Anatomie der Haussäugetiere. Schattauer; Stuttgart, Germany: 2005. Faszien Und Muskeln Des Kopfes Und Stammes; pp. 101–140.

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