Analyze Diet
Veterinary medicine international2017; 2017; 6059485; doi: 10.1155/2017/6059485

Proinflammatory and Anabolic Gene Expression Effects of Platelet-Rich Gel Supernatants on Equine Synovial Membrane Explants Challenged with Lipopolysaccharide.

Abstract: Platelet-rich plasma (PRP) preparations are used in horses with osteoarthritis (OA). However, some controversies remain regarding the ideal concentration of platelets and leukocytes to produce an adequate anti-inflammatory and anabolic response in the synovial membrane. The aims of this study were to study the influence of leukoconcentrated platelet-rich gel (Lc-PRG) and leukoreduced platelet-rich gel (Lr-PRG) supernatants on the quantitative expression of some proinflammatory and anabolic genes in equine synovial membrane explants (SMEs) challenged with lipopolysaccharide (LPS). SMEs from six horses were cultured over 96 h. Then, SMEs were harvested for RNA extraction and quantitative gene expression analysis by RT-qPCR for nuclear factor kappa B (NFκB), matrix metalloproteinase 13 (MMP-13), a disintegrin and metalloproteinase with thrombospondin motifs 4 (ADAMTS-4), collagen type I alpha 1 (COL1A1), collagen type II alpha 1 (COL2A1), and cartilage oligomeric matrix protein (COMP). The 25% and 50% Lc-PRG supernatants led to downregulation of NFκB, MMP-13, ADAMTS-4, COL1A1, COL2A1, and COMP in SMEs. Lr-PRG supernatants (particularly at the 50% concentration) induced downregulation of NFκB, MMP-13, ADAMTS-4, and COL1A1 and upregulation of COL2A1 and COMP. Lr-PRG supernatants should be used for the treatment of inflammatory arthropathies in horses because they have anti-inflammatory and anabolic effects in the synovial membrane.
Publication Date: 2017-07-06 PubMed ID: 28761774PubMed Central: PMC5518502DOI: 10.1155/2017/6059485Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • 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 investigates how platelet-rich plasma treatments, with varying concentrations of platelets and leukocytes, can impact anti-inflammatory and anabolic responses in horses suffering from osteoarthritis. It concludes that leukoreduced platelet-rich gel supernatants have beneficial effects on the synovial membrane, making them a suitable treatment for inflammatory arthropathies in horses.

Study Objective

  • The purpose of this study was to examine how leukoconcentrated platelet-rich gel (Lc-PRG) and leukoreduced platelet-rich gel (Lr-PRG) supernatants affect the expression of proinflammatory and anabolic genes in equine synovial membrane explants (SMEs), which had been challenged using lipopolysaccharide (LPS).

Methodology

  • Researchers used SMEs from six horses and cultured them over a period of 96 hours. These SMEs were subsequently harvested for RNA extraction.
  • RT-qPCR was employed for the analysis of quantitative gene expression. The genes investigated were nuclear factor kappa B (NFB), matrix metalloproteinase 13 (MMP-13), a disintegrin and metalloproteinase with thrombospondin motifs 4 (ADAMTS-4), collagen type I alpha 1 (COL1A1), collagen type II alpha 1 (COL2A1), and cartilage oligomeric matrix protein (COMP).

Findings

  • The study found that 25% and 50% Lc-PRG supernatants led to a reduction in the expression of NFB, MMP-13, ADAMTS-4, COL1A1, COL2A1, and COMP genes in SMEs.
  • Interestingly, Lr-PRG supernatants, particularly at concentrations of 50%, induced a decrease in NFB, MMP-13, ADAMTS-4, and COL1A1 gene expression while at the same time increasing the expression of COL2A1 and COMP.

Conclusions

  • The research concluded that Lr-PRG supernatants, owing to their ability to suppress proinflammatory gene expression and stimulate anabolic gene expression, should be used in the treatment of inflammatory arthropathies in horses. This is due to their demonstrated anti-inflammatory and anabolic effects on the synovial membrane.

Cite This Article

APA
Carmona JU, Ríos DL, López C, Álvarez ME, Pérez JE. (2017). Proinflammatory and Anabolic Gene Expression Effects of Platelet-Rich Gel Supernatants on Equine Synovial Membrane Explants Challenged with Lipopolysaccharide. Vet Med Int, 2017, 6059485. https://doi.org/10.1155/2017/6059485

Publication

ISSN: 2090-8113
NlmUniqueID: 101524203
Country: United States
Language: English
Volume: 2017
Pages: 6059485

Researcher Affiliations

Carmona, Jorge U
  • Grupo de Investigación Terapia Regenerativa, Departamento de Salud Animal, Universidad de Caldas, Manizales, Colombia.
Ríos, Diana L
  • Grupo de Investigación Terapia Regenerativa, Departamento de Salud Animal, Universidad de Caldas, Manizales, Colombia.
López, Catalina
  • Grupo de Investigación Terapia Regenerativa, Departamento de Salud Animal, Universidad de Caldas, Manizales, Colombia.
Álvarez, María E
  • Grupo de Investigación Terapia Regenerativa, Departamento de Salud Animal, Universidad de Caldas, Manizales, Colombia.
  • Grupo de Investigación Biosalud, Departamento de Ciencias Básicas para la Salud, Universidad de Caldas, Manizales, Colombia.
Pérez, Jorge E
  • Grupo de Investigación Biosalud, Departamento de Ciencias Básicas para la Salud, Universidad de Caldas, Manizales, Colombia.

References

This article includes 35 references
  1. Sadabad H. N., Behzadifar M., Arasteh F., Behzadifar M., Dehghan H. R.. Efficacy of Platelet-Rich Plasma versus Hyaluronic Acid for treatment of Knee Osteoarthritis: a systematic review and meta-analysis.. Electronic Physician 2016;8(3):2115–2122.
    doi: 10.19082/2115pmc: PMC4844477pubmed: 27123220google scholar: lookup
  2. Brossi P. M., Moreira J. J., Machado T. S., Baccarin R. Y.. Platelet-rich plasma in orthopedic therapy: a comparative systematic review of clinical and experimental data in equine and human musculoskeletal lesions.. BMC Veterinary Research 2015;11(1):98–148.
    doi: 10.1186/s12917-015-0403-zpmc: PMC4449579pubmed: 25896610google scholar: lookup
  3. Mirza M. H., Bommala P., Richbourg H. A., Rademacher N., Kearney M. T., Lopez M. J. G.. Gait Changes Vary among Horses with Naturally Occurring Osteoarthritis Following Intra-articular Administration of Autologous Platelet-Rich Plasma.. Frontiers in Veterinary Science 2016;3.
    doi: 10.3389/fvets.2016.00029pmc: PMC4829588pubmed: 27148544google scholar: lookup
  4. Rios D. L., López C., Álvarez M. E., Samudio I. J., Carmona J. U.. Effects over time of two platelet gel supernatants on growth factor, cytokine and hyaluronan concentrations in normal synovial membrane explants challenged with lipopolysaccharide.. BMC Musculoskeletal Disorders 2015.
    doi: 10.1186/s12891-015-0605-3pmc: PMC4475292pubmed: 26092588google scholar: lookup
  5. Tyrnenopoulou P., Diakakis N., Karayannopoulou M., Savvas I., Koliakos G.. Evaluation of intra-articular injection of autologous platelet lysate (PL) in horses with osteoarthritis of the distal interphalangeal joint.. Veterinary Quarterly 2016;36(2):56–62.
    doi: 10.1080/01652176.2016.1141257pubmed: 26828234google scholar: lookup
  6. Broeckx S., Zimmerman M., Crocetti S.. Regenerative therapies for equine degenerative joint disease: a preliminary study.. PLoS ONE 2014;9(1).
  7. Knop E., Paula L. E., Fuller R.. Platelet-rich plasma for osteoarthritis treatment.. Revista Brasileira de Reumatologia (English Edition) 2016;56(2):152–164.
    doi: 10.1016/j.rbre.2015.07.002pubmed: 27267529google scholar: lookup
  8. Rios D. L., López C., Carmona J. U.. Evaluation of the anti-inflammatory effects of two platelet-rich gel supernatants in an in vitro system of cartilage inflammation.. Cytokine 2015;76(2):505–513.
    doi: 10.1016/j.cyto.2015.07.008pubmed: 26185893google scholar: lookup
  9. Ehrenfest D. M. D., Andia I., Zumstein M. A., Zhang C.-Q., Pinto N. R., Bielecki T.. Classification of platelet concentrates (Platelet-Rich Plasma-PRP, Platelet-Rich Fibrin-PRF) for topical and infiltrative use in orthopedic and sports medicine: current consensus, clinical implications and perspectives.. Muscles, Ligaments and Tendons Journal 2014;4(1):3–9.
    pmc: PMC4049647pubmed: 24932440
  10. Ehrenfest D. M. D., Bielecki T., Jimbo R.. Do the fibrin architecture and leukocyte content influence the growth factor release of platelet concentrates? An evidence-based answer comparing a pure Platelet-Rich Plasma (P-PRP) gel and a leukocyte- and Platelet-Rich Fibrin (L-PRF). Current Pharmaceutical Biotechnology 2012;13(7):1145–1152.
    doi: 10.2174/138920112800624382pubmed: 21740377google scholar: lookup
  11. Assirelli E., Filardo G., Mariani E.. Effect of two different preparations of platelet-rich plasma on synoviocytes.. Knee Surgery, Sports Traumatology, Arthroscopy 2014.
    doi: 10.1007/s00167-014-3113-3pmc: PMC4541703pubmed: 24942296google scholar: lookup
  12. Carmona J. U., Ríos D. L., López C., Álvarez M. E., Pérez J. E., Bohórquez M. E.. In vitro effects of platelet-rich gel supernatants on histology and chondrocyte apoptosis scores, hyaluronan release and gene expression of equine cartilage explants challenged with lipopolysaccharide.. BMC Veterinary Research 2016;12(1, article 135).
    doi: 10.1186/s12917-016-0759-8pmc: PMC4929746pubmed: 27369779google scholar: lookup
  13. Braun H. J., Kim H. J., Chu C. R., Dragoo J. L.. The effect of platelet-rich plasma formulations and blood products on human synoviocytes: Implications for intra-articular injury and therapy.. The American Journal of Sports Medicine 2014;42(5):1204–1210.
    doi: 10.1177/0363546514525593pmc: PMC5878923pubmed: 24634448google scholar: lookup
  14. Filardo G., Kon E., Pereira Ruiz M. T.. Platelet-rich plasma intra-articular injections for cartilage degeneration and osteoarthritis: single-versus double-spinning approach.. Knee Surgery, Sports Traumatology, Arthroscopy 2012;20(10):2082–2091.
    doi: 10.1007/s00167-011-1837-xpubmed: 22203046google scholar: lookup
  15. Arguelles D., Carmona J. U., Pastor J.. Evaluation of single and double centrifugation tube methods for concentrating equine platelets.. Research in Veterinary Science 2006;81(2):237–245.
    doi: 10.1016/j.rvsc.2005.12.008pubmed: 16969921google scholar: lookup
  16. Byron C. R., Orth M. W., Venta P. J., Lloyd J. W., Caron J. P.. Influence of glucosamine on matrix metalloproteinase expression and activity in lipopolysaccharide-stimulated equine chondrocytes.. American Journal of Veterinary Research 2003;64(6):666–671.
    doi: 10.2460/ajvr.2003.64.666pubmed: 12828249google scholar: lookup
  17. Penha-Goncalves M. N., Onions D. E., Nicolson L.. Cloning and sequencing of equine transforming growth factor-beta 1 (TGFβ-1) cDNA.. Mitochondrial DNA 1997;7(6):375–378.
    doi: 10.3109/10425179709034059pubmed: 9524819google scholar: lookup
  18. Donnelly B. P., Nixon A. J., Haupt J. L., Dahlgren L. A.. Nucleotide structure of equine platelet-derived growth factor-A and -B and expression in horses with induced acute tendinitis.. The American Journal of Veterinary Research 2006;67(7):1218–1225.
    doi: 10.2460/ajvr.67.7.1218pubmed: 16817746google scholar: lookup
  19. Giraldo C. E., Álvarez M. E., Carmona J. U.. Effects of sodium citrate and acid citrate dextrose solutions on cell counts and growth factor release from equine pure-platelet rich plasma and pure-platelet rich gel.. BMC Veterinary Research 2015;11(1, article 60).
    doi: 10.1186/s12917-015-0370-4pmc: PMC4364319pubmed: 25889052google scholar: lookup
  20. Giraldo C. E., López C., Álvarez M. E., Samudio I. J., Prades M., Carmona J. U.. Effects of the breed, sex and age on cellular content and growth factor release from equine pure-platelet rich plasma and pure-platelet rich gel.. BMC Veterinary Research 2013;9, article 29.
    doi: 10.1186/1746-6148-9-29pmc: PMC3577464pubmed: 23402541google scholar: lookup
  21. Livak K. J., Schmittgen T. D.. Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method.. Methods 2001;25(4):402–408.
    doi: 10.1006/meth.2001.1262pubmed: 11846609google scholar: lookup
  22. Aicher W., Pap T., Gay S.. Laminin-modulierte Entzündungsreaktionen in synovialen Fibroblasten von Rheumapatienten.. Zeitschrift für Rheumatologie 2008;67(1):59–61.
    doi: 10.1007/s00393-008-0261-1pubmed: 18214499google scholar: lookup
  23. Sadatsuki R., Kaneko H., Kinoshita M.. Perlecan is required for the chondrogenic differentiation of synovial mesenchymal cells through regulation of Sox9 gene expression.. Journal of Orthopaedic Research 2016.
    doi: 10.1002/jor.23318pubmed: 27238423google scholar: lookup
  24. Tang H., Chen W., Chiang C., Chen L., Chang Y., Chen C.. Differentiation effects of platelet-rich plasma concentrations on synovial fluid mesenchymal stem cells from pigs cultivated in alginate complex hydrogel.. International Journal of Molecular Sciences 2015;16(8):18507–18521.
    doi: 10.3390/ijms160818507pmc: PMC4581257pubmed: 26262616google scholar: lookup
  25. Hermeto L. C., DeRossi R., Oliveira R. J.. Effects of intra-articular injection of mesenchymal stem cells associated with platelet-rich plasma in a rabbit model of osteoarthritis.. Genetics and Molecular Research 2016;15(3).
    doi: 10.4238/gmr.15038569pubmed: 27706690google scholar: lookup
  26. Millward-Sadler S. J., Wright M. O., Davies L. W., Nuki G., Salter D. M.. Mechanotransduction via integrins and interleukin-4 results in altered aggrecan and matrix metalloproteinase 3 gene expression in normal, but not osteoarthritic, human articular chondrocytes.. Arthritis & Rheumatism 2000;43(9):2091–2099.
  27. Bolt D. M., Ishihara A., Weisbrode S. E., Bertone A. L.. Effects of triamcinolone acetonide, sodium hyaluronate, amikacin sulfate, and mepivacaine hydrochloride, alone and in combination, on morphology and matrix composition of lipopolysaccharide-challenged and unchallenged equine articular cartilage explants.. American Journal of Veterinary Research 2008;69(7):861–867.
    doi: 10.2460/ajvr.69.7.861pubmed: 18593234google scholar: lookup
  28. Xu Z., Yin W., Zhang Y.. Comparative evaluation of leukocyte- and platelet-rich plasma and pure platelet-rich plasma for cartilage regeneration.. Scientific Reports 2017;7:p. 43301.
    doi: 10.1038/srep43301pmc: PMC5339695pubmed: 28265109google scholar: lookup
  29. Yin W.-J., Xu H.-T., Sheng J.-G.. Advantages of pure platelet-rich plasma compared with leukocyte- and platelet-rich plasma in treating rabbit knee osteoarthritis.. Medical Science Monitor 2016;22:1280–1290.
    doi: 10.12659/MSM.898218pmc: PMC4837928pubmed: 27086145google scholar: lookup
  30. Sundman E. A., Cole B. J., Karas V.. The anti-inflammatory and matrix restorative mechanisms of platelet-rich plasma in osteoarthritis.. American Journal of Sports Medicine 2014;42(1):35–41.
    doi: 10.1177/0363546513507766pubmed: 24192391google scholar: lookup
  31. Carmona J. U., Argüelles D., Climent F., Prades M.. Autologous platele t concentrates as a treatment of horses with osteoarthritis: a preliminary pilot clinical study.. Journal of Equine Veterinary Science 2007;27(4):167–170.
  32. Premer C., Blum A., Bellio M. A.. Allogeneic mesenchymal stem cells restore endothelial function in heart failure by stimulating endothelial progenitor cells.. EBioMedicine 2015;2(5):467–475.
    doi: 10.1016/j.ebiom.2015.03.020pmc: PMC4485912pubmed: 26137590google scholar: lookup
  33. Hare J. M., Fishman J. E., Gerstenblith G.. Comparison of allogeneic vs autologous bone marrow-derived mesenchymal stem cells delivered by transendocardial injection in patients with ischemic cardiomyopathy: the POSEIDON randomized trial.. JAMA 2012;308(22):2369–2379.
    doi: 10.1001/jama.2012.25321pmc: PMC4762261pubmed: 23117550google scholar: lookup
  34. van der Meer P. F., Seghatchian J., Marks D. C.. Quality standards, safety and efficacy of blood-derived serum eye drops: a review.. Transfusion and Apheresis Science 2016;54(1):164–167.
    doi: 10.1016/j.transci.2016.01.022pubmed: 26847866google scholar: lookup
  35. Kawase T.. Platelet-rich plasma and its derivatives as promising bioactive materials for regenerative medicine: basic principles and concepts underlying recent advances.. Odontology 2015;103(2):126–135.
    doi: 10.1007/s10266-015-0209-2pubmed: 26040505google scholar: lookup

Citations

This article has been cited 5 times.
  1. Carmona JU, López C, Argüelles D. Addressing Heterogeneity in Equine PRP Therapies: A Scoping Review of Methods, Evidence, and Commercial Validation. Animals (Basel) 2025 Dec 13;15(24).
    doi: 10.3390/ani15243586pubmed: 41463871google scholar: lookup
  2. Gallego M, López C, Carmona JU. Evaluation of the Pro-, Anti-Inflammatory, and Anabolic Effects of Autologous Platelet-Rich Gel Supernatants in an in vitro Coculture System of Canine Osteoarthritis. Vet Med Int 2022;2022:3377680.
    doi: 10.1155/2022/3377680pubmed: 35449726google scholar: lookup
  3. Camargo Garbin L, Lopez C, Carmona JU. A Critical Overview of the Use of Platelet-Rich Plasma in Equine Medicine Over the Last Decade. Front Vet Sci 2021;8:641818.
    doi: 10.3389/fvets.2021.641818pubmed: 33869321google scholar: lookup
  4. Boffa A, Previtali D, Di Laura Frattura G, Vannini F, Candrian C, Filardo G. Evidence on ankle injections for osteochondral lesions and osteoarthritis: a systematic review and meta-analysis. Int Orthop 2021 Feb;45(2):509-523.
    doi: 10.1007/s00264-020-04689-5pubmed: 32647968google scholar: lookup
  5. Gilbertie JM, Long JM, Schubert AG, Berglund AK, Schaer TP, Schnabel LV. Pooled Platelet-Rich Plasma Lysate Therapy Increases Synoviocyte Proliferation and Hyaluronic Acid Production While Protecting Chondrocytes From Synoviocyte-Derived Inflammatory Mediators. Front Vet Sci 2018;5:150.
    doi: 10.3389/fvets.2018.00150pubmed: 30023361google scholar: lookup