Abstract: Autologous protein solution (APS) has been used anecdotally for intralesional treatment of tendon and ligament injuries, however, its use in these injuries has never been studied . Our objective was to evaluate the effect of APS on tendon healing in an equine superficial digital flexor (SDF) tendonitis model. We hypothesized intralesional injection of APS would result in superior structural and biomechanical healing. SDF tendonitis was induced in both forelimbs of eight horses using collagenase injection. One forelimb was randomly assigned to receive an intralesional injection of APS, while the other was injected with saline. Ultrasonographic examinations were performed at weeks -1, 0, 2, 4, 8, and 12 following treatment. At 12 weeks, horses were euthanized and SDF samples harvested. Histologic evaluation, biomechanical testing, gene expression analysis, total glycosaminoglycan (GAG) and total DNA quantification were performed. Collagen type III () expression was significantly higher ( = 0.028) in saline treated tendon than in normal tendon. Otherwise, there were no significant differences in gene expression. There were no significant differences in histologic or ultrasonographic scores between groups. Mean total DNA content was significantly higher ( = 0.024) in saline treated tendons than normal tendons, whereas total DNA content was not significantly different between APS treated tendon and normal tendon. Elastic modulus was higher in APS treated than saline treated tendon, but the difference was not significant. Reduced expression of in APS treated tendon may indicate superior healing. Increased total DNA content in saline treated tendon may indicate ongoing healing processes, vs. APS treated tendons which may be in the later stages of healing. Limitations include a relatively short study period and inconsistency in size and severity of induced lesions. Intralesional injection of APS resulted in some improvements in healing characteristics.
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This research sought to understand the effects of autologous protein solution (APS) on the healing of tendon injuries in horses. The study specifically focused on tendonitis in the superficial digital flexor (SDF) of horses, comparing the results of APS treatment with a control group that received a saline treatment.
Research Methodology
The study involved eight horses whose SDF tendonitis was artificially induced using collagenase injections in both forelimbs.
One forelimb in each horse was chosen at random to receive an APS treatment, while the other received a saline injection. This ensured each horse served as its own control, adding robustness to the experiment.
Follow-ups were conducted via ultrasonographic examinations over a period of 12 weeks.
At the end of the 12 week period, the horses were euthanized and the SDF samples harvested for further examination.
The harvested tendons were subjected to histologic evaluations, biomechanical testing, gene expression analysis, total glycosaminoglycan (GAG) and total DNA quantification to understand the healing process and effects of the treatment.
Findings
The study found that the collagen type III gene (COL3A1) expression was significantly higher in the tendons treated with saline. However, there were no other significant differences in gene expression between the two groups.
Both histologic and ultrasonographic scores showed no significant differences between APS and saline treated groups.
The mean total DNA content was significantly higher in the saline-treated tendons compared to the normal values. On the other hand, the total DNA content of tendons treated with APS was not significantly different from normal tendons.
While the elastic modulus, a measure of the tendon’s resistance to elastic deformation, was higher in the APS treated tendons than the saline-treated ones, the difference was not statistically significant.
Conclusions and Implications
The reduced COL3A1 gene expression and the normal DNA content in the APS treated tendons may indicate better healing compared to the saline-treated tendons.
The researchers suggest the ongoing higher DNA synthesis in the saline-treated tendons may indicate that these tissues are still in a healing phase, while the APS treated ones may already be in the later stages of healing.
However, they note the limitations of the study including a short study period and inconsistency in the severity of induced lesions.
The study concluded that while APS treatments did show improvements in certain healing characteristics, further research is required to determine its effectiveness conclusively.
Cite This Article
APA
Gaesser AM, Underwood C, Linardi RL, Even KM, Reef VB, Shetye SS, Mauck RL, King WJ, Engiles JB, Ortved KF.
(2021).
Evaluation of Autologous Protein Solution Injection for Treatment of Superficial Digital Flexor Tendonitis in an Equine Model.
Front Vet Sci, 8, 697551.
https://doi.org/10.3389/fvets.2021.697551
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States.
Underwood, Claire
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States.
Linardi, Renata L
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States.
Even, Kayla M
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States.
Reef, Virginia B
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States.
Shetye, Snehal S
McKay Orthopaedic Research Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Mauck, Robert L
McKay Orthopaedic Research Laboratory, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
King, William J
Owl Manor, Warsaw, IN, United States.
Engiles, Julie B
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States.
Department of Pathobiology, New Bolton Center, School of Veterinary Medicine, University of Pennyslvania, Philadelphia, PA, United States.
Ortved, Kyla F
Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, PA, United States.
Grant Funding
U01 TR002953 / NCATS NIH HHS
Conflict of Interest Statement
WK is the Director of Research and Development at Owl Manor, who's product was investigated in this study. The remaining 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.
Muir SM, Reisbig N, Baria M, Kaeding C, Bertone AL. The Concentration of Plasma Provides Additional Bioactive Proteins in Platelet and Autologous Protein Solutions.. Am J Sports Med 2019 Jul;47(8):1955-1963.
Woodell-May J, Matuska A, Oyster M, Welch Z, O'Shaughnessey K, Hoeppner J. Autologous protein solution inhibits MMP-13 production by IL-1β and TNFα-stimulated human articular chondrocytes.. J Orthop Res 2011 Sep;29(9):1320-6.
Favata M. Scarless Healing in the Fetus: Implications and Strategies for Postnatal Tendon Repair. (2006).
Farndale RW, Sayers CA, Barrett AJ. A direct spectrophotometric microassay for sulfated glycosaminoglycans in cartilage cultures.. Connect Tissue Res 1982;9(4):247-8.
Dahlgren LA, Mohammed HO, Nixon AJ. Temporal expression of growth factors and matrix molecules in healing tendon lesions.. J Orthop Res 2005 Jan;23(1):84-92.
Genç E, Beytemur O, Yuksel S, Eren Y, Çağlar A, Küçükyıldırım BO, Güleç MA. Investigation of the biomechanical and histopathological effects of autologous conditioned serum on healing of Achilles tendon.. Acta Orthop Traumatol Turc 2018 May;52(3):226-231.
Jones GC, Corps AN, Pennington CJ, Clark IM, Edwards DR, Bradley MM, Hazleman BL, Riley GP. Expression profiling of metalloproteinases and tissue inhibitors of metalloproteinases in normal and degenerate human achilles tendon.. Arthritis Rheum 2006 Mar;54(3):832-42.
Rees SG, Flannery CR, Little CB, Hughes CE, Caterson B, Dent CM. Catabolism of aggrecan, decorin and biglycan in tendon.. Biochem J 2000 Aug 15;350 Pt 1(Pt 1):181-8.
Kashiwagi M, Enghild JJ, Gendron C, Hughes C, Caterson B, Itoh Y, Nagase H. Altered proteolytic activities of ADAMTS-4 expressed by C-terminal processing.. J Biol Chem 2004 Mar 12;279(11):10109-19.
Dickinson SC, Vankemmelbeke MN, Buttle DJ, Rosenberg K, Heinegård D, Hollander AP. Cleavage of cartilage oligomeric matrix protein (thrombospondin-5) by matrix metalloproteinases and a disintegrin and metalloproteinase with thrombospondin motifs.. Matrix Biol 2003 May;22(3):267-78.
Kain CC, Russell JE, Rouse AM, Manske PR. Regional differences in matrix formation in the healing flexor tendon.. Clin Orthop Relat Res 1988 Apr;(229):308-12.
Attia M, Scott A, Carpentier G, Lian O, Van Kuppevelt T, Gossard C, Papy-Garcia D, Tassoni MC, Martelly I. Greater glycosaminoglycan content in human patellar tendon biopsies is associated with more pain and a lower VISA score.. Br J Sports Med 2014 Mar;48(6):469-75.
Spurlock GH, Spurlock SL, Parker GA. Ultrasonographic, gross, and histologic evaluation of a tendinitis disease model in the horse. Vet Radiol (1989) 30:184–8.
Zedler S, Schaer T, Ebling A, Richardson D. Evaluation of a novel model of equine superficial digital flexor tendonitis in regenerative tendon research. Vet Surg (2008) 37:E34.
Soltanfar A, Meimandi Parizi A, Foad-Noorbakhsh M, Sayyari M, Iraji A. The healing effects of thymoquinone on experimentally induced traumatic tendinopathy in rabbits. J Orthop Surg Res 2023 Mar 23;18(1):233.
Najeb M, Samy A, Rizk A, Mosbah E, Karrouf G. Regenerative biologics modulating inflammation and promoting tenogenesis in equine superficial digital flexor tendonitis: from molecular pathways to clinical translation. Ir Vet J 2025 Sep 17;78(1):21.
Najeb M, Samy A, Rizk A, Mosbah E, Karrouf G. Clinical benefits of early-stage autologous conditioned serum and injectable platelet-rich fibrin on healing superficial digital flexor tendonitis in donkeys. Ir Vet J 2025 Jun 7;78(1):13.