外用硝酸甘油对大鼠背侧皮瓣模型新生血管生成和非蒂生存能力的影响。

0 MEDICINE, RESEARCH & EXPERIMENTAL
Oğuzhan Karakoç, Selman Hakkı Altuntaş, İlkay Armağan
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引用次数: 0

摘要

当游离组织移植不可行时,内插皮瓣经常用于重建手术,但由于对椎弓根的依赖,它们需要分阶段进行。皮瓣的自主化,即移植组织发展新的血管连接并独立于其蒂存活的过程,是分裂前必不可少的。虽然延迟技术、高压氧(HBO)、血管内皮生长因子(VEGF)和干细胞疗法等方法已被测试用于促进血管生成,但外用硝酸甘油(NTG)的作用尚未被研究,硝酸甘油是一种具有血管扩张、抗炎和血管生成特性的一氧化氮(NO)供体。本研究旨在评价外用NTG对大鼠背侧皮瓣模型新生血管生成和皮瓣自主功能的影响。Wistar-Albino大鼠60只,随机分为5组(n = 12)。所有动物的3×3厘米带尾蒂的背侧皮瓣均升高。1 ~ 3组于第5天切除椎弓根,第1组先给予凡士林治疗,第2组先给予NTG治疗5 d后再给予凡士林治疗,第3组继续给予NTG治疗。第4组和第5组在第5天处死,以评估凡士林或NTG后早期血管生成情况。用ImageJ分析皮瓣存活,用VEGF、CD34和CD105染色分析血管生成,用苏木精和伊红(H&E)和马松三色染色分析组织学。2组(485.5 mm²)和3组(757.3 mm²)皮瓣存活率显著高于1组(273.5 mm²),以3组最高(p < 0.01)。ntg处理组VEGF、CD34、CD105表达升高,其中3组血管生成最强。第5组血管增殖明显高于第4组(p < 0.001)。组织学显示,NTG减少上皮破坏、出血、胶原降解和白细胞浸润,同时增强血管增殖。总之,持续外用NTG促进血管生成和加速皮瓣自主化,导致蒂分裂后更大的活力。NTG可能有助于缩短蒂分裂间隔和改善重建手术的结果,但需要进一步的分子和临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of topical nitroglycerin on neoangiogenesis and pedicle-independent viability in a rat dorsal skin flap model.

Interpolated flaps are frequently used in reconstructive surgery when free tissue transfer is not feasible, but they require staged procedures due to pedicle dependence. Flap autonomization, the process by which transferred tissue develops new vascular connections and survives independently of its pedicle, is essential before division. Although methods such as delay techniques, hyperbaric oxygen (HBO), vascular endothelial growth factor (VEGF), and stem cell therapies have been tested to enhance angiogenesis, the effect of topical nitroglycerin (NTG), a nitric oxide (NO) donor with vasodilatory, anti-inflammatory, and angiogenic properties, has not been investigated. This study aimed to evaluate the effect of topical NTG on neoangiogenesis and flap autonomization in a rat dorsal skin flap model. Sixty Wistar-Albino rats were divided into five groups (n = 12). A 3×3 cm dorsal flap with a caudal pedicle was elevated in all animals. In Groups 1-3, pedicles were transected on day 5: Group 1 received vaseline, Group 2 received NTG for 5 days then vaseline, and Group 3 received NTG continuously. Groups 4 and 5 were sacrificed on day 5 to assess early angiogenesis after vaseline or NTG. Flap survival was analyzed with ImageJ, angiogenesis with VEGF, CD34, and CD105 staining, and histology with Hematoxylin and Eosin (H&E) and Masson's Trichrome. Flap survival was significantly greater in Groups 2 (485.5 mm²) and 3 (757.3 mm²) than in Group 1 (273.5 mm²), with Group 3 highest (p < 0.01). NTG-treated groups showed increased VEGF, CD34, and CD105 expression, with the strongest angiogenesis in Group 3. Group 5 also had higher vascular proliferation than Group 4 (p < 0.001). Histology showed that NTG reduced epithelial disruption, hemorrhage, collagen degradation, and leukocytic infiltration while enhancing vascular proliferation. In conclusion, continuous topical NTG enhanced angiogenesis and accelerated flap autonomization, leading to greater viability after pedicle division. NTG may help shorten pedicle division intervals and improve outcomes in reconstructive surgery, but further molecular and clinical studies are needed.

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