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10.1186/s13018-018-0781-6

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suck abstract from ncbi


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pmid29622010
      J+Orthop+Surg+Res 2018 ; 13 (1 ): 72
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  • Mechanical barriers and transforming growth factor beta inhibitor on epidural fibrosis in a rabbit laminectomy model #MMPMID29622010
  • Albiñana-Cunningham JN ; Ripalda-Cemboráin P ; Labiano T ; Echeveste JI ; Granero-Moltó F ; Alfonso-Olmos M
  • J Orthop Surg Res 2018[Apr]; 13 (1 ): 72 PMID29622010 show ga
  • BACKGROUND: TGF-? has been described as a mediator of fibrosis and scarring. Several studies achieved reduction in experimental scarring through the inhibition of TGF-?. Fibroblasts have been defined as the cell population originating fibrosis, blocking fibroblast invasion may impair epidural fibrosis appearance. For this purpose, biocompatible materials used as mechanical barriers and a TGF-? inhibitor peptide were evaluated in the reduction of epidural fibrosis. METHODS: A L6 laminectomy was performed in 40 New Zealand white rabbits. Divided into four groups, each rabbit was assigned to receive either collagen sponge scaffold (CS group), gelatin-based gel (GCP group), P144® (iTGF? group), or left untreated (control group). Four weeks after surgery, cell density, collagen content, and new bone formation of the scar area were determined by histomorphometry. Two experienced pathologists scored dura mater adhesion, scar density, and inflammatory infiltrate in a blinded manner. RESULTS: In all groups, laminectomy site was filled with fibrous tissue and the dura mater presented adhesions. Only GCP group presented a significant reduction in collagen content and scar density. CONCLUSION: GCP treatment reduces epidural fibrosis although did not prevent dura mater adhesion completely.
  • |Animals [MESH]
  • |Biocompatible Materials [MESH]
  • |Cicatrix/etiology/pathology/prevention & control [MESH]
  • |Collagen/metabolism [MESH]
  • |Disease Models, Animal [MESH]
  • |Dura Mater/metabolism/pathology [MESH]
  • |Epidural Space/metabolism/*pathology [MESH]
  • |Fibrosis [MESH]
  • |Laminectomy/*adverse effects [MESH]
  • |Male [MESH]
  • |Organic Chemicals/therapeutic use [MESH]
  • |Peptide Fragments/*therapeutic use [MESH]
  • |Rabbits [MESH]
  • |Receptors, Transforming Growth Factor beta/*therapeutic use [MESH]
  • |Tissue Adhesions/etiology/pathology/*prevention & control [MESH]


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