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Characteristics of Animal Shoulder Models for Rotator Cuff Experiments

  • Kim, Min-Cheol (Department of Orthopaedic Surgery, Chonnam National University Medical School) ;
  • Kim, Myung-Sun (Department of Orthopaedic Surgery, Chonnam National University Medical School)
  • Received : 2014.07.29
  • Accepted : 2014.11.30
  • Published : 2015.03.30

Abstract

Animal shoulder models are important in the investigation of the natural history of various pathologic conditions and for evaluation of the effectiveness of different treatments and biomaterials. The characteristics of animal shoulder models that may be used for rotator cuff related experiments are different with regard to the anatomy, behavioral pattern, advantages and disadvantages in application to each other. The lower primates and all the non-primate species, except the tree kangaroo, were neither functional overhead nor had a true rotator cuff. Utilizing more advanced primates, or perhaps even the tree kangaroo would be ideal and the most relevant to man as they possess a true rotator cuff. However, ethical concerns, costs, and many limitations in obtaining primates generally preclude the use of these animals for such research. Finally we should consider the differences in comparative anatomy and behavioral pattern of each animal model during performance or interpretation of rotator cuff experiments.

Keywords

References

  1. Toussaint B, Schnaser E, Bosley J, Lefebvre Y, Gobezie R. Early structural and functional outcomes for arthroscopic doublerow transosseous-equivalent rotator cuff repair. Am J Sports Med. 2011;39(6):1217-25. https://doi.org/10.1177/0363546510397725
  2. Koh KH, Kang KC, Lim TK, Shon MS, Yoo JC. Prospective randomized clinical trial of single-versus double-row suture anchor repair in 2-to 4-cm rotator cuff tears: clinical and magnetic resonance imaging results. Arthroscopy. 2011;27(4):453-62. https://doi.org/10.1016/j.arthro.2010.11.059
  3. Tashjian RZ, Hollins AM, Kim HM, et al. Factors affecting healing rates after arthroscopic double-row rotator cuff repair. Am J Sports Med. 2010;38(12):2435-42. https://doi.org/10.1177/0363546510382835
  4. Visser LC, Arnoczky SP, Caballero O, Gardner KL. Evaluation of the use of an autologous platelet-rich fibrin membrane to enhance tendon healing in dogs. Am J Vet Res. 2011;72(5):699-705. https://doi.org/10.2460/ajvr.72.5.699
  5. Lyras D, Kazakos K, Verettas D, et al. Immunohistochemical study of angiogenesis after local administration of platelet-rich plasma in a patellar tendon defect. Int Orthop. 2010;34(1):143-8. https://doi.org/10.1007/s00264-009-0728-y
  6. Ricchetti ET, Aurora A, Iannotti JP, Derwin KA. Scaffold devices for rotator cuff repair. J Shoulder Elbow Surg. 2012;21(2):251-65. https://doi.org/10.1016/j.jse.2011.10.003
  7. Kidd KR, Dal Ponte DB, Kellar RS, Williams SK. A comparative evaluation of the tissue responses associated with polymeric implants in the rat and mouse. J Biomed Mater Res. 2002;59(4):682-9. https://doi.org/10.1002/jbm.10032
  8. Patil SD, Papadmitrakopoulos F, Burgess DJ. Concurrent delivery of dexamethasone and VEGF for localized inflammation control and angiogenesis. J Control Release. 2007;117(1):68-79. https://doi.org/10.1016/j.jconrel.2006.10.013
  9. Laschke MW, Haufel JM, Thorlacius H, Menger MD. New experimental approach to study host tissue response to surgical mesh materials in vivo. J Biomed Mater Res A. 2005;74(4):696-704.
  10. Thomsen P, Bjursten LM, Ericson LE. Implants in the abdominal wall of the rat. Scand J Plast Reconstr Surg. 1986;20(2):173-82. https://doi.org/10.3109/02844318609006316
  11. Badylak S, Kokini K, Tullius B, Simmons-Byrd A, Morff R. Morphologic study of small intestinal submucosa as a body wall repair device. J Surg Res. 2002;103(2):190-202. https://doi.org/10.1006/jsre.2001.6349
  12. Zheng F, Lin Y, Verbeken E, et al. Host response after reconstruction of abdominal wall defects with porcine dermal collagen in a rat model. Am J Obstet Gynecol. 2004;191(6):1961-70. https://doi.org/10.1016/j.ajog.2004.01.091
  13. Konstantinovic ML, Lagae P, Zheng F, Verbeken EK, De Ridder D, Deprest JA. Comparison of host response to polypropylene and non-cross-linked porcine small intestine serosal-derived collagen implants in a rat model. BJOG. 2005;112(11):1554-60. https://doi.org/10.1111/j.1471-0528.2005.00688.x
  14. Derwin KA, Badylak SF, Steinmann SP, Iannotti JP. Extracellular matrix scaffold devices for rotator cuff repair. J Shoulder Elbow Surg. 2010;19(3):467-76. https://doi.org/10.1016/j.jse.2009.10.020
  15. Claerhout F, Verbist G, Verbeken E, Konstantinovic M, De Ridder D, Deprest J. Fate of collagen-based implants used in pelvic floor surgery: a 2-year follow-up study in a rabbit model. Am J Obstet Gynecol. 2008;198(1):94.e1-6. https://doi.org/10.1016/j.ajog.2007.05.032
  16. Cook JL, Fox DB, Kuroki K, Jayo M, De Deyne PG. In vitro and in vivo comparison of five biomaterials used for orthopedic soft tissue augmentation. Am J Vet Res. 2008;69(1):148-56. https://doi.org/10.2460/ajvr.69.1.148
  17. Gimbel JA, Van Kleunen JP, Williams GR, Thomopoulos S, Soslowsky LJ. Long durations of immobilization in the rat result in enhanced mechanical properties of the healing supraspinatus tendon insertion site. J Biomech Eng. 2007;129(3):400-4.
  18. Thomopoulos S, Williams GR, Soslowsky LJ. Tendon to bone healing: differences in biomechanical, structural, and compositional properties due to a range of activity levels. J Biomech Eng. 2003;125(1):106-13. https://doi.org/10.1115/1.1536660
  19. Thomopoulos S, Das R, Birman V, et al. Fibrocartilage tissue engineering: the role of the stress environment on cell morphology and matrix expression. Tissue Eng Part A. 2011;17(7-8):1039-53. https://doi.org/10.1089/ten.tea.2009.0499
  20. Bedi A, Kawamura S, Ying L, Rodeo SA. Differences in tendon graft healing between the intra-articular and extra-articular ends of a bone tunnel. HSS J. 2009;5(1):51-7. https://doi.org/10.1007/s11420-008-9096-1
  21. Amiel D, Harwood FL, Gelberman RH, Chu CR, Seiler JG 3rd, Abrahamsson S. Autogenous intrasynovial and extrasynovial tendon grafts: an experimental study of pro alpha 1(I) collagen mRNA expression in dogs. J Orthop Res. 1995;13(3):459-63. https://doi.org/10.1002/jor.1100130321
  22. Meddahi A, Bree F, Papy-Garcia D, Gautron J, Barritault D, Caruelle JP. Pharmacological studies of RGTA(11), a heparan sulfate mimetic polymer, efficient on muscle regeneration. J Biomed Mater Res. 2002;62(4):525-31. https://doi.org/10.1002/jbm.10283
  23. Sonnabend DH, Young AA. Comparative anatomy of the rotator cuff. J Bone Joint Surg Br. 2009;91(12):1632-7.
  24. Liu X, Manzano G, Kim HT, Feeley BT. A rat model of massive rotator cuff tears. J Orthop Res. 2011;29(4):588-95. https://doi.org/10.1002/jor.21266
  25. Ide J, Kikukawa K, Hirose J, Iyama K, Sakamoto H, Mizuta H. The effects of fibroblast growth factor-2 on rotator cuff reconstruction with acellular dermal matrix grafts. Arthroscopy. 2009;25(6):608-16. https://doi.org/10.1016/j.arthro.2008.11.011
  26. Uezono K, Ide J, Tokunaga T, Sakamoto H, Okamoto N, Mizuta H. Effect of immobilization on rotator cuff reconstruction with acellular dermal matrix grafts in an animal model. J Shoulder Elbow Surg. 2013;22(9):1290-7. https://doi.org/10.1016/j.jse.2012.12.037
  27. Rowshan K, Hadley S, Pham K, Caiozzo V, Lee TQ, Gupta R. Development of fatty atrophy after neurologic and rotator cuff injuries in an animal model of rotator cuff pathology. J Bone Joint Surg Am. 2010;92(13):2270-8. https://doi.org/10.2106/JBJS.I.00812
  28. Gerber C, Meyer DC, Nuss KM, Farshad M. Anabolic steroids reduce muscle damage caused by rotator cuff tendon release in an experimental study in rabbits. J Bone Joint Surg Am. 2011;93(23):2189-95. https://doi.org/10.2106/JBJS.J.01589
  29. Kimura A, Aoki M, Fukushima S, Ishii S, Yamakoshi K. Reconstruction of a defect of the rotator cuff with polytetrafluoroethylene felt graft. Recovery of tensile strength and histocompatibility in an animal model. J Bone Joint Surg Br. 2003;85(2):282-7. https://doi.org/10.1302/0301-620X.85B2.12823
  30. Derwin KA, Codsi MJ, Milks RA, Baker AR, McCarron JA, Iannotti JP. Rotator cuff repair augmentation in a canine model with use of a woven poly-L-lactide device. J Bone Joint Surg Am. 2009;91(5):1159-71. https://doi.org/10.2106/JBJS.H.00775
  31. Derwin KA, Baker AR, Spragg RK, Leigh DR, Iannotti JP. Commercial extracellular matrix scaffolds for rotator cuff tendon repair. Biomechanical, biochemical, and cellular properties. J Bone Joint Surg Am. 2006;88(12):2665-72. https://doi.org/10.2106/JBJS.E.01307
  32. Smith MJ, Cook JL, Kuroki K, et al. Comparison of a novel bone-tendon allograft with a human dermis-derived patch for repair of chronic large rotator cuff tears using a canine model. Arthroscopy. 2012;28(2):169-77. https://doi.org/10.1016/j.arthro.2011.08.296
  33. Adams JE, Zobitz ME, Reach JS Jr, An KN, Steinmann SP. Rotator cuff repair using an acellular dermal matrix graft: an in vivo study in a canine model. Arthroscopy. 2006;22(7):700-9. https://doi.org/10.1016/j.arthro.2006.03.016
  34. Sonnabend DH, Howlett CR, Young AA. Histological evaluation of repair of the rotator cuff in a primate model. J Bone Joint Surg Br. 2010;92(4):586-94.

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