Zhu Haifeng, Wei Xiaofei, Bian Ka, Murad Ferid
Department of Integrative Biology and Pharmacology, Institute of Molecular Medicine, The University of Texas-Health Science Center at Houston, Texas 77030, USA.
J Burn Care Res. 2008 Sep-Oct;29(5):804-14. doi: 10.1097/BCR.0b013e3181848119.
Increasing evidence showed the important role of nitric oxide (NO) in skin repair and reconstruction. In this report, we investigated the effects of NO on 2nd degree burn wound of mice with a newly developed topical NO-gel. Using regular hematoxylin&eosin staining and immunohistochemistry, we determined the effects of NO on wound closure, hair follicle regeneration, collagen deposition, angiogenesis, and inflammatory cell infiltration in the wound of mice during wound healing. NO treatment significantly accelerated re-epithelialization by 50%, which has resulted in a markedly faster wound closure than that in control group. NO significantly promoted follicle stem cell recruitment, a key player in re-epithelialization. In addition, hair follicle regeneration also was enhanced by NO treatment in mice. As we have reported with rat model, NO treatment significantly increased the number of procollagen-expressing fibroblasts, which peaked by day 10 after burn wound. We also demonstrated an increase of angiogenesis in NO treated wounds compared with that in the control group during wound healing. Finally, we found that the NO gel promoted wound bed infiltration and retention of inflammatory cells that are a major source of growth factors and cytokines during the healing processes. These observations suggest that NO released from a topical preparation has the potential to enhance burn wound healing by regulation of many cellular processes in the skin.
越来越多的证据表明一氧化氮(NO)在皮肤修复和重建中发挥着重要作用。在本报告中,我们使用新开发的局部用NO凝胶研究了NO对小鼠二度烧伤创面的影响。通过常规苏木精和伊红染色以及免疫组织化学,我们确定了NO在伤口愈合过程中对小鼠伤口闭合、毛囊再生、胶原蛋白沉积、血管生成和炎症细胞浸润的影响。NO治疗使再上皮化显著加速了50%,这导致伤口闭合明显快于对照组。NO显著促进了毛囊干细胞募集,这是再上皮化的关键因素。此外,NO治疗还增强了小鼠的毛囊再生。正如我们在大鼠模型中所报道的,NO治疗显著增加了表达前胶原蛋白的成纤维细胞数量,在烧伤创面后第10天达到峰值。我们还证明,在伤口愈合过程中,与对照组相比,NO处理的伤口血管生成有所增加。最后,我们发现NO凝胶促进了伤口床炎症细胞的浸润和滞留,而炎症细胞是愈合过程中生长因子和细胞因子的主要来源。这些观察结果表明,局部制剂释放的NO有可能通过调节皮肤中的许多细胞过程来促进烧伤创面愈合。