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Contractile behavior of the forelimb digital flexors during steady-state locomotion in horses (Equus caballus): an initial test of muscle architectural hypotheses about in vivo function.

Abstract: The forelimb digital flexors of the horse display remarkable diversity in muscle architecture despite each muscle-tendon unit having a similar mechanical advantage across the fetlock joint. We focus on two distinct muscles of the digital flexor system: short compartment deep digital flexor (DDF(sc)) and the superficial digital flexor (SDF). The objectives were to investigate force-length behavior and work performance of these two muscles in vivo during locomotion, and to determine how muscle architecture contributes to in vivo function in this system. We directly recorded muscle force (via tendon strain gauges) and muscle fascicle length (via sonomicrometry crystals) as horses walked (1.7 m s(-1)), trotted (4.1 m s(-1)) and cantered (7.0 m s(-1)) on a motorized treadmill. Over the range of gaits and speeds, DDF(sc) fascicles shortened while producing relatively low force, generating modest positive net work. In contrast, SDF fascicles initially shortened, then lengthened while producing high force, resulting in substantial negative net work. These findings suggest the long fibered, unipennate DDF(sc) supplements mechanical work during running, whereas the short fibered, multipennate SDF is specialized for economical high force and enhanced elastic energy storage. Apparent in vivo functions match well with the distinct architectural features of each muscle.
Publication Date: 2008-09-20 PubMed ID: 18835360DOI: 10.1016/j.cbpa.2008.09.007Google Scholar: Lookup
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  • Clinical Trial
  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.

Summary

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This study investigates the distinct contributions of two muscles in a horse’s limb during locomotion – the short compartment deep digital flexor (DDF(sc)) and the superficial digital flexor (SDF). The study finds that DDF(sc), a long, unipennate muscle, generates low force but performs positive work, while the shorter, multipennate SDF generates high force and accomplishes negative work.

Overview of the Research

  • This research focuses on the different roles and contributions of the DDF(sc) and SDF muscles during the locomotion of horses. Despite both muscles operating across the fetlock joint and being part of the digital flexor system, they display great variation in their muscle architecture.
  • Employing direct methods of measurement through tendon strain gauges and sonomicrometry crystals, the researchers captured data on muscle force and muscle fascicle length while horses performed different gaits (walking, trotting and cantering) on a motorized treadmill.

Findings of the Research

  • The results from the tests showed that DDF(sc) fascicles shortened while producing low force and generated moderate positive work across all the gaits and speeds tested.
  • On the contrary, the SDF fascicles initially shortened but then lengthened and produced high levels of force, resulting in a significant amount of negative net work.

Meaning of the Research

  • The observations and results from the study shed light on the underlying in vivo functions of these two muscles during the locomotion of horses.
  • The DDF(sc) with its long fibers and unipennate architecture, aids in mechanical work during running, while the shorter, multipennate SDF specializes in high force production and enhanced elastic energy storage for economical performance.
  • The distinct in vivo functions match well with the different architectural features of the DDF(sc) and SDF muscles, implying that muscle architecture plays an essential role in function.

Cite This Article

APA
Butcher MT, Hermanson JW, Ducharme NG, Mitchell LM, Soderholm LV, Bertram JE. (2008). Contractile behavior of the forelimb digital flexors during steady-state locomotion in horses (Equus caballus): an initial test of muscle architectural hypotheses about in vivo function. Comp Biochem Physiol A Mol Integr Physiol, 152(1), 100-114. https://doi.org/10.1016/j.cbpa.2008.09.007

Publication

ISSN: 1531-4332
NlmUniqueID: 9806096
Country: United States
Language: English
Volume: 152
Issue: 1
Pages: 100-114

Researcher Affiliations

Butcher, M T
  • Department of Biological Sciences, Youngstown State University, Youngstown, OH 44555, USA. mtbutcher@ysu.edu
Hermanson, J W
    Ducharme, N G
      Mitchell, L M
        Soderholm, L V
          Bertram, J E A

            MeSH Terms

            • Animals
            • Biomechanical Phenomena
            • Elasticity
            • Electromyography
            • Forelimb / physiology
            • Gait / physiology
            • Horses / physiology
            • Locomotion / physiology
            • Models, Biological
            • Muscle Contraction / physiology
            • Muscles / anatomy & histology
            • Muscles / physiology
            • Organ Size
            • Weight-Bearing / physiology

            Citations

            This article has been cited 9 times.
            1. Harrison SM, Whitton RC, Stover SM, Symons JE, Cleary PW. A Coupled Biomechanical-Smoothed Particle Hydrodynamics Model for Horse Racing Tracks. Front Bioeng Biotechnol 2022;10:766748.
              doi: 10.3389/fbioe.2022.766748pubmed: 35265590google scholar: lookup
            2. Mossor AM, Austin BL, Avey-Arroyo JA, Butcher MT. A Horse of a Different Color?: Tensile Strength and Elasticity of Sloth Flexor Tendons. Integr Org Biol 2020;2(1):obaa032.
              doi: 10.1093/iob/obaa032pubmed: 33796818google scholar: lookup
            3. García Liñeiro JA, Graziotti GH, Rodríguez Menéndez JM, Ríos CM, Affricano NO, Victorica CL. Parameters and functional analysis of the deep epaxial muscles in the thoracic, lumbar and sacral regions of the equine spine. J Anat 2018 Jul;233(1):55-63.
              doi: 10.1111/joa.12818pubmed: 29708263google scholar: lookup
            4. Raiteri BJ, Cresswell AG, Lichtwark GA. Muscle-tendon length and force affect human tibialis anterior central aponeurosis stiffness in vivo. Proc Natl Acad Sci U S A 2018 Apr 3;115(14):E3097-E3105.
              doi: 10.1073/pnas.1712697115pubmed: 29555756google scholar: lookup
            5. Skalec A, Egerbacher M. The deep fascia and retinacula of the equine forelimb - structure and innervation. J Anat 2017 Sep;231(3):405-416.
              doi: 10.1111/joa.12643pubmed: 28585281google scholar: lookup
            6. Youngstrom DW, Rajpar I, Kaplan DL, Barrett JG. A bioreactor system for in vitro tendon differentiation and tendon tissue engineering. J Orthop Res 2015 Jun;33(6):911-8.
              doi: 10.1002/jor.22848pubmed: 25664422google scholar: lookup
            7. Butcher MT, Bertram JE, Syme DA, Hermanson JW, Chase PB. Frequency dependence of power and its implications for contractile function of muscle fibers from the digital flexors of horses. Physiol Rep 2014 Oct 1;2(10).
              doi: 10.14814/phy2.12174pubmed: 25293602google scholar: lookup
            8. Youngstrom DW, Barrett JG, Jose RR, Kaplan DL. Functional characterization of detergent-decellularized equine tendon extracellular matrix for tissue engineering applications. PLoS One 2013;8(5):e64151.
              doi: 10.1371/journal.pone.0064151pubmed: 23724028google scholar: lookup
            9. Butcher MT, Chase PB, Hermanson JW, Clark AN, Brunet NM, Bertram JE. Contractile properties of muscle fibers from the deep and superficial digital flexors of horses. Am J Physiol Regul Integr Comp Physiol 2010 Oct;299(4):R996-R1005.
              doi: 10.1152/ajpregu.00510.2009pubmed: 20702801google scholar: lookup