Aşula M Fatih, Onur I Umut, Yigit F Ulviye
Department of Ophthalmology, Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Tevfik Saglam Caddesi No: 11 Zuhuratbaba, 34147, Istanbul, Turkey.
Int Ophthalmol. 2019 Jul;39(7):1553-1558. doi: 10.1007/s10792-018-0964-5. Epub 2018 Jul 13.
Fumagillin has been previously used to treat corneal microsporidial keratitis and also identified as an angiogenesis inhibitor. This study aimed to evaluate efficacy of fumagillin bicyclohexylamine on the rat model of corneal neovascularization induced by silver nitrate cauterization.
Twenty-four Albino Wistar rats (n = 24) were divided into three groups. Following silver nitrate-induced corneal injury, eyes in Group 1 received one drop of 5 mg/mL topical fumagillin bicyclohexylamine four times daily for 10 days. Group 2 received subconjunctival injection of 0.1 mL fumagillin bicyclohexylamine (2.5 mg/mL) on day 1 and day 5. Group 3 received artificial tears and lubricants four times daily for 10 days as control. On day 10, animals were sacrificed. Corneal specimens were obtained and prepared to assess vascular endothelial growth factor (VEGF-C) levels and corneal angiogenic microvessel density.
There was no significant difference in VEGF-C levels between the groups (P = 0.994). Assessment of angiogenic microvessel density for peripheral corneal zone also did not reveal significant difference between the groups (P = 0.113). However, mean vascular density in Group 1 and Group 2 was significantly higher for both midperipheral and central corneal zones in comparison with Group 3 (P = 0.003, P = 0.015).
Previously proved to be effective for treatment of microsporidial keratitis in humans, topical and subconjunctival concentration or dosing of fumagillin bicyclohexylamine failed to reduce corneal neovascularization induced by silver nitrate in this study. Further studies comparing different concentrations and dosing may detect inhibitory effects of fumagillin on corneal neovascularization without inducing toxicity.
烟曲霉素先前已用于治疗角膜微孢子虫性角膜炎,并且还被鉴定为一种血管生成抑制剂。本研究旨在评估烟曲霉素双环己胺对硝酸银烧灼诱导的大鼠角膜新生血管模型的疗效。
将24只白化Wistar大鼠(n = 24)分为三组。在硝酸银诱导角膜损伤后,第1组的眼睛每天接受4次一滴5mg/mL的局部烟曲霉素双环己胺,持续10天。第2组在第1天和第5天接受0.1mL烟曲霉素双环己胺(2.5mg/mL)的结膜下注射。第3组每天接受4次人工泪液和润滑剂,持续10天作为对照。在第10天,处死动物。获取角膜标本并制备以评估血管内皮生长因子(VEGF-C)水平和角膜血管生成微血管密度。
各组之间VEGF-C水平无显著差异(P = 0.994)。对角膜周边区血管生成微血管密度的评估也未显示各组之间有显著差异(P = 0.113)。然而,与第3组相比,第1组和第2组中周边和中央角膜区的平均血管密度均显著更高(P = 0.003,P = 0.015)。
先前已证明对人类微孢子虫性角膜炎有效,本研究中局部和结膜下浓度或剂量的烟曲霉素双环己胺未能减少硝酸银诱导的大鼠角膜新生血管。进一步比较不同浓度和剂量的研究可能会发现烟曲霉素对角膜新生血管的抑制作用而不产生毒性。