Transcorneal Freezing in Aged Rabbits as a Platform for Evaluating Corneal Endothelial Cell Therapeutics.

Lauren E Cornell, Eric J Snider, Jennifer S McDaniel, Randolph Glickman, Anthony Johnson, David Zamora
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Abstract

Purpose: Transcorneal freezing is a common technique used in rabbits to induce damage to the corneal endothelium. Previous studies have been performed with a range of freezing temperatures, times, and rabbit ages. Here, we aimed to characterize the aged rabbit endothelium after transcorneal freezing to establish an innate corneal endothelial cell regrowth rate and propose it as a mechanism for evaluation of therapeutic efficacy in rabbit models.

Methods: Central corneas of anesthetized New Zealand White rabbits (n=3) aged 18-24 months were exposed to nitrous oxide cooled probes for 30 seconds. Animals were assessed by in vivo confocal microscopy, applanation tonometry, specular microscopy, optical coherence tomography, and histology. The contralateral eye acted as a control. Images were taken immediately before and after injury and on days 2, 4, 7, 11, and 14.

Results: Following transcorneal freezing, there was a significant decrease in corneal endothelium density and a temporary increase in corneal thickness. Endothelial density decreased by 95% immediately after injury compared to controls and showed linear recovery over 14 days, reaching a 38% reduction by day 14. There was a significant increase in pleomorphism across all time points post-injury. Conversely, corneal thickness increased two days post injury but recovered at all later time points. Intraocular pressure was not affected throughout.

Conclusions: This corneal endothelium injury platform is ideal for injury and therapeutic research as it can be rapidly performed, and has minimal impact on corneal thickness and intraocular pressure. Due to innate rabbit endothelial regrowth, it is vital to establish corneal endothelial recovery rate before evaluating therapeutics for efficacy in this model system.

老化兔经角膜冷冻作为评估角膜内皮细胞治疗的平台。
目的:经角膜冷冻是兔角膜内皮损伤的常用方法。以前的研究是在冷冻温度、时间和兔子年龄的范围内进行的。在此,我们旨在对经角膜冷冻后的衰老兔内皮进行表征,以建立先天性角膜内皮细胞再生速率,并提出将其作为兔模型治疗效果评估的机制。方法:18 ~ 24月龄麻醉的新西兰大白兔(n=3只)中央角膜暴露于氧化亚氮冷却探针中30秒。动物通过体内共聚焦显微镜、压平眼压测量、镜面显微镜、光学相干断层扫描和组织学进行评估。对侧眼睛作为对照。分别于伤前、伤后及第2、4、7、11、14天拍摄图像。结果:经角膜冷冻后,角膜内皮细胞密度明显降低,角膜厚度暂时增加。与对照组相比,内皮细胞密度在损伤后立即下降95%,并在14天内呈现线性恢复,到第14天达到38%。损伤后各时间点多形性显著增加。相反,角膜厚度在损伤后2天增加,但在之后的所有时间点都恢复了。整个过程中眼压未受影响。结论:该角膜内皮损伤平台操作快捷,对角膜厚度和眼压影响小,是理想的损伤和治疗研究平台。由于兔内皮细胞的先天再生,在该模型系统中评估治疗方法的疗效之前,建立角膜内皮细胞的恢复速率是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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