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A dipeptidyl peptidase‐4 inhibitor promotes wound healing in normoglycemic mice by modulating keratinocyte activity

机译:通过调节角质形成细胞活性,二肽肽肽酶-4抑制剂促进正常血糖小鼠中的伤口愈合

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摘要

Abstract Dipeptidyl peptidase‐4 ( DPP ‐4) inhibitors are a well‐known and novel class of oral antihyperglycaemic drugs. DPP ‐4 inhibition facilitates ulcer healing in patients with diabetes. However, the actual mechanisms, which are independent of lower blood glucose levels, are still unknown. Therefore, the aim of this study was to analyse the effect of the DPP ‐4 inhibitor sitagliptin on wound healing through a glucose‐independent pathway. In this study, DPP ‐4 inhibitors facilitate keratinocyte differentiation and the proliferation, increase blood flow in the cutaneous of wounds in healthy C57BL/6 mice. Additionally, the administration of the DPP ‐4 inhibitor ameliorates wound healing and enhances adiponectin expression in healthy C57BL/6 mice. Taken together, our results reveal a protective role for the DPP ‐4 inhibitor sitagliptin in wound healing by regulating adiponectin and phospho‐ eNOS levels in keratinocytes. Based on these results, the DPP ‐4 inhibitor may have therapeutic potential for healing wounds through a diabetes‐independent mechanism.
机译:摘要二肽肽酶-4(DPP-4)抑制剂是一种众所周知的和新型的口腔抗血糖药物。 DPP -4抑制有助于糖尿病患者的溃疡愈合。然而,与血糖水平无关的实际机制仍然未知。因此,本研究的目的是通过葡萄糖无关的途径分析DPP -4抑制剂SITAGLIPTIN对伤口愈合的影响。在本研究中,DPP -4抑制剂促进了角质形成细胞分化和增殖,增加了健康C57BL / 6小鼠中的伤口中的血液流动。另外,DPP -4抑制剂的给药改善伤口愈合,并增强健康C57BL / 6小鼠中的脂联素表达。我们的结果表明,通过调节角质形成细胞中的脂联素和磷酸酶水平,揭示了DPP -4抑制剂SITAGLIPIN在伤口愈合中的保护作用。基于这些结果,DPP -4抑制剂可具有通过糖尿病无关机制愈合伤口的治疗潜力。

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