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沙利度胺类似物对兔角膜新生血管的抑制作用。

The inhibitory effect of thalidomide analogue on corneal neovascularization in rabbits.

机构信息

Department of Ophthalmology and Visual Science, St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Cornea. 2013 Aug;32(8):1142-8. doi: 10.1097/ICO.0b013e318292a79d.

DOI:10.1097/ICO.0b013e318292a79d
PMID:23739149
Abstract

PURPOSE

To evaluate the effect of thalidomide analogue CC-3052 on corneal neovascularization in the rabbit model.

METHODS

Corneal neovascularization was induced in 15 rabbits by a silk suture in the corneal stroma. At 1 week after suturing, 30 eyes were divided into 5 groups of 6 eyes each. Three groups were treated with topical CC-3052 at 3 different concentrations: 0.25% (group 1), 0.5% (group 2), and 1.0% (group 3). All treatments were performed twice a day for a week. A 0.5% concentration of CC-3052 was injected subconjunctivally once in group 4. In group 5, a topical balanced salt solution was added twice a day for a week as the experimental control group. Rabbit corneas were photographed by a digital camera and examined by the operating microscope. Half of the corneal specimens were analyzed histopathologically, and the other half were used to measure the concentration of tumor necrosis factor α and vascular endothelial growth factor (VEGF) messenger RNA by reverse transcriptase-polymerase chain reaction.

RESULTS

The neovascularized area was decreased in all treatment groups compared with the control group. There was a significant difference in the percentage and score of corneal neovascularization between the control and all treatment groups. Inflammation, fibroblast, neovascularization, and anti-VEGF antibody intensities were significantly lower in the control group. The concentration of VEGF and tumor necrosis factor α was significantly lower in the control group. There was no difference between the treatment groups.

CONCLUSIONS

Topical and subconjunctival administration of thalidomide analogue CC-3052 was found to be effective for the inhibition of corneal neovascularization.

摘要

目的

评估沙利度胺类似物 CC-3052 对兔角膜新生血管的作用。

方法

通过角膜基质中的丝线缝合诱导 15 只兔子的角膜新生血管。在缝合后 1 周,将 30 只眼睛分为 5 组,每组 6 只。三组分别用三种不同浓度的 CC-3052 滴眼:0.25%(第 1 组)、0.5%(第 2 组)和 1.0%(第 3 组)。所有治疗均每天两次,持续一周。第 4 组结膜下注射 0.5%浓度的 CC-3052 一次。第 5 组作为实验组,每天滴加平衡盐溶液两次,持续一周作为实验对照组。用数码相机拍摄兔角膜照片,并用手术显微镜检查。半角膜标本进行组织病理学分析,另一半用于通过逆转录聚合酶链反应测量肿瘤坏死因子-α和血管内皮生长因子(VEGF)信使 RNA 的浓度。

结果

与对照组相比,所有治疗组的新生血管面积均减少。对照组与所有治疗组的角膜新生血管百分比和评分均有显著差异。对照组的炎症、成纤维细胞、新生血管和抗 VEGF 抗体强度明显较低。对照组 VEGF 和肿瘤坏死因子-α的浓度明显较低。治疗组之间没有差异。

结论

局部和结膜下给予沙利度胺类似物 CC-3052 可有效抑制角膜新生血管形成。

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