Department and Graduate Institute of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Tri-Service General Hospital Penghu Branch, National Defense Medical Center, Penghu, Taiwan.
Int Wound J. 2024 Oct;21(10):e70083. doi: 10.1111/iwj.70083.
Deep and extensive wounds usually cannot be closed directly by suturing or skin grafting. Flap transplantation is typically used to reconstruct large wounds clinically. The flap survival is based on a stable blood perfusion. It is established that estrogen promotes wound healing and angiogenesis, and regulates the inflammatory response, leading to enhanced flap survival after transplantation. However, estrogen concentrations administered in previous studies were significantly higher than physiological levels, potentially causing systemic side effects. Estrogen-sustained-release silastic capsules can maintain blood serum estrogen closer to physiological levels. This study aimed to investigate whether administering estrogen at a lower concentration, closer to physiological levels, could still enhance flap survival.
This study was performed in a random skin flap model in ovariectomized (OVX) mice. Sustained-release estrogen silastic capsules were implanted into OVX mice to determine the functional role of estrogen in wound healing after flap transplantation. Flap blood perfusion was analysed using a colour laser Doppler scanner. Immunohistochemical staining of CD31, hypoxia-inducible factor 1 alpha (HIF-1α), alpha-smooth muscle actin (α-SMA), cleaved caspase 3 and apoptotic terminal dUTP nick end-labelling stain was used to investigate flap angiogenesis, tissue hypoxia, wound healing and cell death in the flap tissue, respectively.
We observed that administering estrogen at a lower concentration enhanced superficial blood perfusion while reducing the flap's ischemic area and tissue necrosis. HIF-1α expression was significantly decreased in the dermis layer but not in the fascia, whereas cleaved caspase 3 levels decreased in the fascia but remained unchanged in the dermis. Additionally, there was no significant difference in CD31and α-SMA expression between the groups.
In summary, the study showed that an estrogen silastic capsule maintained physiological estrogen levels and improved superficial perfusion, thereby reducing dermal hypoxia, and cell death in a mouse random pattern skin flap model. Although no significant promotion of angiogenesis was observed, the study suggests that appropriate estrogen supplements could enhance flap wound recovery.
深度和广泛的伤口通常不能直接通过缝合或植皮来闭合。临床上通常采用皮瓣移植来重建大伤口。皮瓣的存活基于稳定的血液灌注。已经证实,雌激素促进伤口愈合和血管生成,并调节炎症反应,从而导致移植后皮瓣存活增加。然而,以前的研究中给予的雌激素浓度明显高于生理水平,可能会导致全身副作用。雌激素持续释放硅酮胶囊可以使血清雌激素水平更接近生理水平。本研究旨在探讨给予较低浓度、更接近生理水平的雌激素是否仍能增强皮瓣的存活。
本研究在去卵巢(OVX)小鼠的随机皮瓣模型中进行。将持续释放雌激素硅酮胶囊植入 OVX 小鼠中,以确定雌激素在皮瓣移植后伤口愈合中的功能作用。使用彩色激光多普勒扫描仪分析皮瓣血液灌注。免疫组织化学染色 CD31、缺氧诱导因子 1 阿尔法(HIF-1α)、α-平滑肌肌动蛋白(α-SMA)、裂解 caspase 3 和凋亡末端 dUTP 缺口末端标记染色分别用于研究皮瓣血管生成、组织缺氧、皮瓣组织中的伤口愈合和细胞死亡。
我们观察到,给予较低浓度的雌激素可增强浅层血液灌注,同时减少皮瓣的缺血区和组织坏死。真皮层中 HIF-1α 的表达显著降低,但筋膜层中没有降低,而筋膜层中裂解 caspase 3 的水平降低,但真皮层中没有改变。此外,两组之间 CD31 和 α-SMA 的表达没有差异。
总之,该研究表明,雌激素硅酮胶囊维持生理雌激素水平并改善浅层灌注,从而减少小鼠随机皮瓣模型中真皮缺氧和细胞死亡。虽然没有观察到明显的血管生成促进作用,但该研究表明,适当的雌激素补充可能会增强皮瓣伤口恢复。