Kim Tae-Im, Kim Sang Woo, Kim Sunwoong, Kim Terry, Kim Eung Kweon
Corneal Dystrophy Research Institute, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.
Cornea. 2008 Apr;27(3):349-52. doi: 10.1097/ICO.0b013e31815cf67d.
To evaluate the effect of subconjunctival bevacizumab (Avastin) administration on corneal neovascularization (NV) in rabbits.
NV was induced by placing a suture at the corneal periphery of the right eye of 20 rabbits. Immediately after suturing and again 1 week later, rabbits were divided into 2 groups and administered a subconjunctival injection of normal saline (control) or bevacizumab (Avastin; 5 mg/0.2 mL), respectively. On day 14, digital photographs of the cornea were taken and analyzed to determine the area of the cornea covered by NV. In addition, immunohistochemical analysis was used to determine CD31 and vascular endothelial growth factor (VEGF) expression in corneal tissue.
Analysis of digital photographs showed that there was less corneal NV in bevacizumab-treated eyes than in controls (P < 0.001, Mann-Whitney U test). In addition, there was less staining for VEGF and CD31 in corneas from bevacizumab-treated eyes than in control eyes. Subconjunctival bevacizumab injections were not associated with any complications during observation.
Subconjunctival bevacizumab administration decreased suture-induced corneal neovascularization in rabbits.
评估结膜下注射贝伐单抗(阿瓦斯汀)对兔角膜新生血管化(NV)的影响。
通过在20只兔右眼的角膜周边放置缝线诱导NV形成。缝合后立即以及1周后,将兔分为2组,分别给予结膜下注射生理盐水(对照组)或贝伐单抗(阿瓦斯汀;5mg/0.2mL)。在第14天,拍摄角膜数码照片并进行分析,以确定NV覆盖的角膜面积。此外,采用免疫组织化学分析来确定角膜组织中CD31和血管内皮生长因子(VEGF)的表达。
数码照片分析显示,贝伐单抗治疗组的角膜NV少于对照组(P<0.001,曼-惠特尼U检验)。此外,贝伐单抗治疗组角膜中VEGF和CD31的染色少于对照组。在观察期间,结膜下注射贝伐单抗未出现任何并发症。
结膜下注射贝伐单抗可减少兔缝线诱导的角膜新生血管化。