Tibial transverse transport promotes diabetic wound healing via angiogenic growth factors, anti-inflammatory response, and progenitor cell mobilization
Introduction: Tibial transverse transport (TTT), a technique derived from the Ilizarov method, has shown clinical efficacy in treating recalcitrant diabetic foot ulcers by promoting angiogenesis. However, its underlying molecular mechanisms remain unclear.
Objectives: This study aimed to investigate the mechanisms by which TTT influences wound healing in a rat model of type 2 diabetes mellitus (T2DM).
Methods: Thirty-six male Sprague–Dawley rats were induced to develop T2DM via a high-fat diet and low-dose streptozotocin. They were randomized into three groups: sham surgery, external fixator application without transport, and active TTT surgery. A full-thickness excisional wound was created on the dorsum of the right foot. Wound area was measured photographically on days 0, 3, 6, 9, 12, and 15. Serum levels of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), platelet-derived growth factor (PDGF), interleukin-10 (IL-10), and granulocyte colony-stimulating factor (G-CSF) were quantified using enzyme-linked immunosorbent assay on days 9 and 15.
Results: The TTT group exhibited a significantly accelerated reduction in wound area from day 9 onwards compared to the sham and fixator groups (p < 0.05). Concomitantly, serum levels of VEGF, bFGF, PDGF, IL-10, and G-CSF were significantly elevated in the TTT group at both time points.
Conclusion: We established a T2DM rat model of TTT surgery. Our findings suggest that the TTT technique accelerates diabetic wound healing, potentially through a multifaceted mechanism involving enhanced serum levels of key angiogenic growth factors, promotion of an anti-inflammatory microenvironment (via IL-10), and mobilization of endothelial progenitor cells (potentially via G-CSF).
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