Roan Jun-Neng, Cheng Han-Ni, Young Chao-Chung, Lee Chi-Ju, Yeh Ming-Long, Luo Chwan-Yau, Tsai Yau-Sheng, Lam Chen-Fuh
Institute of Clinical Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Division of Cardiovascular Surgery, Department of Surgery, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Department of Anesthesiology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
J Surg Res. 2017 Feb;208:93-103. doi: 10.1016/j.jss.2016.09.024. Epub 2016 Sep 17.
Diabetes disregulates inflammatory responses and impairs vascular function in wounds. Glucagon-like peptide-1 receptor (Glp-1R) agonists are hypoglycemic agents with pleiotropic vascular protective and anti-inflammatory effects. The therapeutic potential of a Glp-1 analogue in a diabetic rat model of excisional wound injury was investigated.
Excisional wounds were created on the dorsum of streptozotocin-induced diabetic rats, which received placebo or Glp-1 analogue exendin-4 (Ex4; 0.5 μg/kg/d, i.p.) for 2 wk. The final-to-initial wound area ratio was measured for 14 d. Levels of superoxide anions and proinflammatory cytokines in the wound were determined. Angiogenesis was assessed using the Matrigel assay. Expression levels of proangiogenic factors and extracellular matrix proteins were measured.
Ex4 restored wound closure in diabetic rats and significantly suppressed the generation of superoxide anions and interleukin-6 in wounds. The number of circulating endothelial progenitor (CD34/KDR) cells increased significantly in Ex4-treated diabetic rats, which also showed increased capillary tube formation. Protein levels of vascular endothelial growth factor receptor-2, phosphorylated endothelial nitric oxide synthase, matrix metalloproteinase-2, and transforming growth factor-β were increased in diabetic rats receiving Ex4 therapy. Ex4-enhanced vascularity, dermal regeneration, and epidermal regeneration, while it decreased hemorrhaging and increased the number of proliferative cells in the dermis.
Ex4 accelerated excisional wound healing in subjects with diabetes. Glp-1R activation attenuates inflammatory response and enhances angiogenesis during the early proliferation phase of wound healing in diabetic subjects, while it enhances transforming growth factor-β/matrix metalloproteinase-mediated regeneration during the maturation phase. These results suggest that Ex4 could be used as a standard hypoglycemic agent in diabetic patients with wound injury.
糖尿病会扰乱炎症反应并损害伤口的血管功能。胰高血糖素样肽-1受体(Glp-1R)激动剂是具有多效性血管保护和抗炎作用的降血糖药物。本研究探讨了一种Glp-1类似物在切除性伤口损伤糖尿病大鼠模型中的治疗潜力。
在链脲佐菌素诱导的糖尿病大鼠背部制造切除性伤口,这些大鼠接受安慰剂或Glp-1类似物艾塞那肽-4(Ex4;0.5μg/kg/d,腹腔注射),持续2周。在14天内测量最终伤口面积与初始伤口面积的比值。测定伤口中超氧阴离子和促炎细胞因子的水平。使用基质胶试验评估血管生成。测量促血管生成因子和细胞外基质蛋白的表达水平。
Ex4恢复了糖尿病大鼠的伤口闭合,并显著抑制了伤口中超氧阴离子和白细胞介素-6的产生。在接受Ex4治疗的糖尿病大鼠中,循环内皮祖细胞(CD34/KDR)数量显著增加,同时毛细血管管形成也增加。接受Ex4治疗的糖尿病大鼠中,血管内皮生长因子受体-2、磷酸化内皮型一氧化氮合酶、基质金属蛋白酶-2和转化生长因子-β的蛋白水平升高。Ex4增强了血管生成、真皮再生和表皮再生,同时减少了出血并增加了真皮中增殖细胞的数量。
Ex4加速了糖尿病患者的切除性伤口愈合。在糖尿病患者伤口愈合的早期增殖阶段,Glp-1R激活可减轻炎症反应并增强血管生成,而在成熟阶段则增强转化生长因子-β/基质金属蛋白酶介导的再生。这些结果表明,Ex可能用作糖尿病伤口损伤患者的标准降糖药物。