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Acta biomaterialia2013; 9(8); 7948-7956; doi: 10.1016/j.actbio.2013.05.004

Helical sub-structures in energy-storing tendons provide a possible mechanism for efficient energy storage and return.

Abstract: The predominant function of tendons is to position the limb during locomotion. Specific tendons also act as energy stores. Energy-storing (ES) tendons are prone to injury, the incidence of which increases with age. This is likely related to their function; ES tendons are exposed to higher strains and require a greater ability to recoil than positional tendons. The specialized properties of ES tendons are thought to be achieved through structural and compositional differences. However, little is known about structure-function relationships in tendons. This study uses fascicles from the equine superficial digital flexor (SDFT) and common digital extensor (CDET) as examples of ES and positional tendons. We hypothesized that extension and recoil behaviour at the micro-level would differ between tendon types, and would alter with age in the injury-prone SDFT. Supporting this, the results show that extension in the CDET is dominated by fibre sliding. By contrast, greater rotation was observed in the SDFT, suggesting a helical component to fascicles in this tendon. This was accompanied by greater recovery and less hysteresis loss in SDFT samples. In samples from aged SDFTs, the amount of rotation and the ability to recover decreased, while hysteresis loss increased. These findings indicate that fascicles in the ES SDFT may have a helical structure, enabling the more efficient recoil observed. Further, the helix structure appears to alter with ageing; this coincides with a reduction in the ability of SDFT fascicles to recoil. This may affect tendon fatigue resistance and predispose aged tendons to injury.
Publication Date: 2013-05-10 PubMed ID: 23669621DOI: 10.1016/j.actbio.2013.05.004Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

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.

This research explores how helical structures in certain types of tendons may contribute to efficient energy storage and recoil. The study uses equine tendons to suggest that these helical structures might deteriorate with age, potentially leading to tendon injury.

Background and Purpose

  • Tendons play a crucial role in locomotion and certain tendons have the specific task of storing energy. These energy-storing (ES) tendons are more prone to injury, with the risk increasing as the tendon ages.
  • ES tendons are generally exposed to higher strains and have a higher requirement for recoil than positional tendons. This specialized feature is thought to be due to differences in structure and composition.
  • The researchers used two types of equine tendons, the Superficial Digital Flexor Tendon (SDFT) and the Common Digital Extensor Tendon (CDET), as examples of ES and positional tendons in their study.
  • The researchers hypothesized that there could be a difference in extension and recoil behavior between the two types of tendons, with these changes particularly noticeable in the injury-prone SDFT as it ages.

Methodology

  • The research examines the behavior of fascicles, small bundles of fibers, from both the SDFT and the CDET.
  • They monitored the extension in the CDET which primarily showed fiber sliding. Conversely, rotation was more evident in the SDFT, signaling a possible helical component to its fascicles.

Key Findings

  • SDFT exhibited a higher recovery rate and less hysteresis loss, which suggests better energy efficiency, compared to the CDET.
  • As the SDFT samples aged, the amount of rotation and its ability to recover diminished, while hysteresis loss increased.
  • The research suggests that the ES SDFT may have a helical structural component that contributes to its efficient recoil.
  • The helix-like structure seems to deteriorate with age, which could correlate with a decline in the SDFT’s ability to recoil. This could have a potential impact on tendon fatigue resistance and may increase the risk of injury in aged tendons.

Implications

  • The research could have numerous implications for the understanding of tendon functionality and the study of age-related tendon injuries.
  • The discovery of the helix-like structure within the ES SDFT helps shed light on the structural differences that enable the tendons to store and efficiently release energy.
  • This research could potentially inform therapeutic and preventive approaches for ES tendon injuries, especially in ageing populations.

Cite This Article

APA
Thorpe CT, Klemt C, Riley GP, Birch HL, Clegg PD, Screen HR. (2013). Helical sub-structures in energy-storing tendons provide a possible mechanism for efficient energy storage and return. Acta Biomater, 9(8), 7948-7956. https://doi.org/10.1016/j.actbio.2013.05.004

Publication

ISSN: 1878-7568
NlmUniqueID: 101233144
Country: England
Language: English
Volume: 9
Issue: 8
Pages: 7948-7956
PII: S1742-7061(13)00236-5

Researcher Affiliations

Thorpe, Chavaunne T
  • Institute of Bioengineering, School of Engineering and Materials Science, Queen Mary, University of London, Mile End Road, London E1 4NS, UK. c.thorpe@qmul.ac.uk
Klemt, Christian
    Riley, Graham P
      Birch, Helen L
        Clegg, Peter D
          Screen, Hazel R C

            MeSH Terms

            • Animals
            • Computer Simulation
            • Elastic Modulus / physiology
            • Energy Transfer / physiology
            • Horses
            • In Vitro Techniques
            • Models, Anatomic
            • Models, Biological
            • Structure-Activity Relationship
            • Tendons / cytology
            • Tendons / physiology
            • Tensile Strength / physiology

            Grant Funding

            • MR/K006312/1 / Medical Research Council

            Citations

            This article has been cited 45 times.
            1. Waugh CM, Mousavizadeh R, Lee J, Screen HRC, Scott A. Mild hypercholesterolemia impacts achilles sub-tendon mechanical properties in young rats.. BMC Musculoskelet Disord 2023 Apr 12;24(1):282.
              doi: 10.1186/s12891-023-06375-0pubmed: 37046262google scholar: lookup
            2. Ostadi Moghaddam A, Arshee MR, Lin Z, Sivaguru M, Phillips H, McFarlin BL, Toussaint KC, Wagoner Johnson AJ. An indentation-based framework for probing the glycosaminoglycan-mediated interactions of collagen fibrils.. J Mech Behav Biomed Mater 2023 Apr;140:105726.
              doi: 10.1016/j.jmbbm.2023.105726pubmed: 36827935google scholar: lookup
            3. Yin NH, Parker AW, Matousek P, Birch HL. Chemical Markers of Human Tendon Health Identified Using Raman Spectroscopy: Potential for In Vivo Assessment.. Int J Mol Sci 2022 Nov 27;23(23).
              doi: 10.3390/ijms232314854pubmed: 36499181google scholar: lookup
            4. Benage LG, Sweeney JD, Giers MB, Balasubramanian R. Dynamic Load Model Systems of Tendon Inflammation and Mechanobiology.. Front Bioeng Biotechnol 2022;10:896336.
              doi: 10.3389/fbioe.2022.896336pubmed: 35910030google scholar: lookup
            5. Golman M, Birman V, Thomopoulos S, Genin GM. Enthesis strength, toughness and stiffness: an image-based model comparing tendon insertions with varying bony attachment geometries.. J R Soc Interface 2021 Dec;18(185):20210421.
              doi: 10.1098/rsif.2021.0421pubmed: 34932930google scholar: lookup
            6. Zhang S, Ju W, Chen X, Zhao Y, Feng L, Yin Z, Chen X. Hierarchical ultrastructure: An overview of what is known about tendons and future perspective for tendon engineering.. Bioact Mater 2022 Feb;8:124-139.
            7. Pierantoni M, Silva Barreto I, Hammerman M, Verhoeven L, Törnquist E, Novak V, Mokso R, Eliasson P, Isaksson H. A quality optimization approach to image Achilles tendon microstructure by phase-contrast enhanced synchrotron micro-tomography.. Sci Rep 2021 Aug 27;11(1):17313.
              doi: 10.1038/s41598-021-96589-wpubmed: 34453067google scholar: lookup
            8. Patel D, Zamboulis DE, Spiesz EM, Birch HL, Clegg PD, Thorpe CT, Screen HRC. Structure-function specialisation of the interfascicular matrix in the human achilles tendon.. Acta Biomater 2021 Sep 1;131:381-390.
              doi: 10.1016/j.actbio.2021.07.019pubmed: 34271169google scholar: lookup
            9. Knaus KR, Blemker SS. 3D Models Reveal the Influence of Achilles Subtendon Twist on Strain and Energy Storage.. Front Bioeng Biotechnol 2021;9:539135.
              doi: 10.3389/fbioe.2021.539135pubmed: 33614608google scholar: lookup
            10. Nash A, Notou M, Lopez-Clavijo AF, Bozec L, de Leeuw NH, Birch HL. Glucosepane is associated with changes to structural and physical properties of collagen fibrils.. Matrix Biol Plus 2019 Nov;4:100013.
              doi: 10.1016/j.mbplus.2019.100013pubmed: 33543010google scholar: lookup
            11. Eekhoff JD, Steenbock H, Berke IM, Brinckmann J, Yanagisawa H, Wagenseil JE, Lake SP. Dysregulated assembly of elastic fibers in fibulin-5 knockout mice results in a tendon-specific increase in elastic modulus.. J Mech Behav Biomed Mater 2021 Jan;113:104134.
              doi: 10.1016/j.jmbbm.2020.104134pubmed: 33045519google scholar: lookup
            12. Lin AH, Allan AN, Zitnay JL, Kessler JL, Yu SM, Weiss JA. Collagen denaturation is initiated upon tissue yield in both positional and energy-storing tendons.. Acta Biomater 2020 Dec;118:153-160.
              doi: 10.1016/j.actbio.2020.09.056pubmed: 33035697google scholar: lookup
            13. Safa BN, Peloquin JM, Natriello JR, Caplan JL, Elliott DM. Helical fibrillar microstructure of tendon using serial block-face scanning electron microscopy and a mechanical model for interfibrillar load transfer.. J R Soc Interface 2019 Nov 29;16(160):20190547.
              doi: 10.1098/rsif.2019.0547pubmed: 31744419google scholar: lookup
            14. Muench JR, Thelen DG, Henak CR. Interfibrillar shear behavior is altered in aging tendon fascicles.. Biomech Model Mechanobiol 2020 Jun;19(3):841-849.
              doi: 10.1007/s10237-019-01251-0pubmed: 31707625google scholar: lookup
            15. Karathanasopoulos N, Ganghoffer JF. Exploiting Viscoelastic Experimental Observations and Numerical Simulations to Infer Biomimetic Artificial Tendon Fiber Designs.. Front Bioeng Biotechnol 2019;7:85.
              doi: 10.3389/fbioe.2019.00085pubmed: 31134193google scholar: lookup
            16. Lee AH, Elliott DM. Multi-Scale Loading and Damage Mechanisms of Plantaris and Rat Tail Tendons.. J Orthop Res 2019 Aug;37(8):1827-1837.
              doi: 10.1002/jor.24309pubmed: 30977538google scholar: lookup
            17. Lee AH, Elliott DM. Comparative multi-scale hierarchical structure of the tail, plantaris, and Achilles tendons in the rat.. J Anat 2019 Feb;234(2):252-262.
              doi: 10.1111/joa.12913pubmed: 30484871google scholar: lookup
            18. Spiesz EM, Thorpe CT, Thurner PJ, Screen HRC. Structure and collagen crimp patterns of functionally distinct equine tendons, revealed by quantitative polarised light microscopy (qPLM).. Acta Biomater 2018 Apr 1;70:281-292.
              doi: 10.1016/j.actbio.2018.01.034pubmed: 29409868google scholar: lookup
            19. Akintunde AR, Miller KS. Evaluation of microstructurally motivated constitutive models to describe age-dependent tendon healing.. Biomech Model Mechanobiol 2018 Jun;17(3):793-814.
              doi: 10.1007/s10237-017-0993-4pubmed: 29234987google scholar: lookup
            20. Picu RC, Deogekar S, Islam MR. Poisson's Contraction and Fiber Kinematics in Tissue: Insight From Collagen Network Simulations.. J Biomech Eng 2018 Feb 1;140(2):0210021-02100212.
              doi: 10.1115/1.4038428pubmed: 29131889google scholar: lookup
            21. Bell JS, Hayes S, Whitford C, Sanchez-Weatherby J, Shebanova O, Vergari C, Winlove CP, Terrill N, Sorensen T, Elsheikh A, Meek KM. The hierarchical response of human corneal collagen to load.. Acta Biomater 2018 Jan;65:216-225.
              doi: 10.1016/j.actbio.2017.11.015pubmed: 29128531google scholar: lookup
            22. Eekhoff JD, Fang F, Kahan LG, Espinosa G, Cocciolone AJ, Wagenseil JE, Mecham RP, Lake SP. Functionally Distinct Tendons From Elastin Haploinsufficient Mice Exhibit Mild Stiffening and Tendon-Specific Structural Alteration.. J Biomech Eng 2017 Nov 1;139(11):1110031-9.
              doi: 10.1115/1.4037932pubmed: 28916838google scholar: lookup
            23. Shearer T, Thorpe CT, Screen HRC. The relative compliance of energy-storing tendons may be due to the helical fibril arrangement of their fascicles.. J R Soc Interface 2017 Aug;14(133).
              doi: 10.1098/rsif.2017.0261pubmed: 28794162google scholar: lookup
            24. Warner JJ, Gillies AR, Hwang HH, Zhang H, Lieber RL, Chen S. 3D-printed biomaterials with regional auxetic properties.. J Mech Behav Biomed Mater 2017 Dec;76:145-152.
              doi: 10.1016/j.jmbbm.2017.05.016pubmed: 28754244google scholar: lookup
            25. Lee AH, Szczesny SE, Santare MH, Elliott DM. Investigating mechanisms of tendon damage by measuring multi-scale recovery following tensile loading.. Acta Biomater 2017 Jul 15;57:363-372.
              doi: 10.1016/j.actbio.2017.04.011pubmed: 28435080google scholar: lookup
            26. Thorpe CT, Riley GP, Birch HL, Clegg PD, Screen HRC. Fascicles and the interfascicular matrix show decreased fatigue life with ageing in energy storing tendons.. Acta Biomater 2017 Jul 1;56:58-64.
              doi: 10.1016/j.actbio.2017.03.024pubmed: 28323176google scholar: lookup
            27. Szczesny SE, Fetchko KL, Dodge GR, Elliott DM. Evidence that interfibrillar load transfer in tendon is supported by small diameter fibrils and not extrafibrillar tissue components.. J Orthop Res 2017 Oct;35(10):2127-2134.
              doi: 10.1002/jor.23517pubmed: 28071819google scholar: lookup
            28. Linderman SW, Gelberman RH, Thomopoulos S, Shen H. Cell and Biologic-Based Treatment of Flexor Tendon Injuries.. Oper Tech Orthop 2016 Sep;26(3):206-215.
              doi: 10.1053/j.oto.2016.06.011pubmed: 28042226google scholar: lookup
            29. Patel D, Sharma S, Bryant SJ, Screen HR. Recapitulating the Micromechanical Behavior of Tension and Shear in a Biomimetic Hydrogel for Controlling Tenocyte Response.. Adv Healthc Mater 2017 Feb;6(4).
              doi: 10.1002/adhm.201601095pubmed: 28026126google scholar: lookup
            30. Thorpe CT, Riley GP, Birch HL, Clegg PD, Screen HRC. Fascicles and the interfascicular matrix show adaptation for fatigue resistance in energy storing tendons.. Acta Biomater 2016 Sep 15;42:308-315.
              doi: 10.1016/j.actbio.2016.06.012pubmed: 27286677google scholar: lookup
            31. Thorpe CT, Karunaseelan KJ, Ng Chieng Hin J, Riley GP, Birch HL, Clegg PD, Screen HR. Distribution of proteins within different compartments of tendon varies according to tendon type.. J Anat 2016 Sep;229(3):450-8.
              doi: 10.1111/joa.12485pubmed: 27113131google scholar: lookup
            32. Fang F, Lake SP. Modelling approaches for evaluating multiscale tendon mechanics.. Interface Focus 2016 Feb 6;6(1):20150044.
              doi: 10.1098/rsfs.2015.0044pubmed: 26855747google scholar: lookup
            33. Kondratko-Mittnacht J, Lakes R, Vanderby R Jr. Shear loads induce cellular damage in tendon fascicles.. J Biomech 2015 Sep 18;48(12):3299-305.
            34. Thorpe CT, Godinho MSC, Riley GP, Birch HL, Clegg PD, Screen HRC. The interfascicular matrix enables fascicle sliding and recovery in tendon, and behaves more elastically in energy storing tendons.. J Mech Behav Biomed Mater 2015 Dec;52:85-94.
              doi: 10.1016/j.jmbbm.2015.04.009pubmed: 25958330google scholar: lookup
            35. Kondratko-Mittnacht J, Duenwald-Kuehl S, Lakes R, Vanderby R Jr. Shear load transfer in high and low stress tendons.. J Mech Behav Biomed Mater 2015 May;45:109-20.
              doi: 10.1016/j.jmbbm.2015.01.021pubmed: 25700261google scholar: lookup
            36. Screen HR, Berk DE, Kadler KE, Ramirez F, Young MF. Tendon functional extracellular matrix.. J Orthop Res 2015 Jun;33(6):793-9.
              doi: 10.1002/jor.22818pubmed: 25640030google scholar: lookup
            37. Connizzo BK, Sarver JJ, Han L, Soslowsky LJ. In situ fibril stretch and sliding is location-dependent in mouse supraspinatus tendons.. J Biomech 2014 Dec 18;47(16):3794-8.
            38. Szczesny SE, Elliott DM. Incorporating plasticity of the interfibrillar matrix in shear lag models is necessary to replicate the multiscale mechanics of tendon fascicles.. J Mech Behav Biomed Mater 2014 Dec;40:325-338.
              doi: 10.1016/j.jmbbm.2014.09.005pubmed: 25262202google scholar: lookup
            39. Slane LC, Thelen DG. Non-uniform displacements within the Achilles tendon observed during passive and eccentric loading.. J Biomech 2014 Sep 22;47(12):2831-5.
            40. Shepherd JH, Riley GP, Screen HR. Early stage fatigue damage occurs in bovine tendon fascicles in the absence of changes in mechanics at either the gross or micro-structural level.. J Mech Behav Biomed Mater 2014 Oct;38:163-72.
              doi: 10.1016/j.jmbbm.2014.06.005pubmed: 25001495google scholar: lookup
            41. Szczesny SE, Edelstein RS, Elliott DM. DTAF dye concentrations commonly used to measure microscale deformations in biological tissues alter tissue mechanics.. PLoS One 2014;9(6):e99588.
              doi: 10.1371/journal.pone.0099588pubmed: 24915570google scholar: lookup
            42. Thorpe CT, Riley GP, Birch HL, Clegg PD, Screen HR. Fascicles from energy-storing tendons show an age-specific response to cyclic fatigue loading.. J R Soc Interface 2014 Mar 6;11(92):20131058.
              doi: 10.1098/rsif.2013.1058pubmed: 24402919google scholar: lookup
            43. Chernak Slane L, Thelen DG. The use of 2D ultrasound elastography for measuring tendon motion and strain.. J Biomech 2014 Feb 7;47(3):750-4.
            44. Shepherd JH, Legerlotz K, Demirci T, Klemt C, Riley GP, Screen HR. Functionally distinct tendon fascicles exhibit different creep and stress relaxation behaviour.. Proc Inst Mech Eng H 2014 Jan;228(1):49-59.
              doi: 10.1177/0954411913509977pubmed: 24285289google scholar: lookup
            45. Birch HL, Thorpe CT, Rumian AP. Specialisation of extracellular matrix for function in tendons and ligaments.. Muscles Ligaments Tendons J 2013 Jan;3(1):12-22.
              doi: 10.11138/mltj/2013.3.1.012pubmed: 23885341google scholar: lookup