4.5 Article

Perspectives for preclinical mouse models of glaucoma after Boston keratoprosthesis type 1

期刊

EXPERIMENTAL EYE RESEARCH
卷 208, 期 -, 页码 -

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.exer.2021.108615

关键词

Boston keratoprosthesis; Glaucoma; Animal model; Miniaturized keratoprosthesis

资金

  1. Fonds de recherche en ophtalmologie de l'Universite de Montreal (FROUM, Universite de Montreal, Montreal, Canada)
  2. Fonds de recherche du Quebec en sante (FRQS)
  3. Vision Health Research Network (Quebec)
  4. McGill's Department of Experimental Surgery
  5. McGill University Faculty of Medicine

向作者/读者索取更多资源

The study aimed to determine the feasibility of establishing a reproducible mouse model of glaucoma after KPro surgery, finding that removing the lens during surgery can reduce the incidence of loss of ocular tone and retinal detachment. Successful mouse KPro surgery may require practice to be a useful and reproducible model, and animal KPro models should be further pursued in future studies.
Animal models of the Boston keratoprosthesis type 1 (KPro) are needed to study glaucoma damage after KPro implantation to control for confounding comorbidities common in human KPro recipients. The purpose of this study was to determine the feasibility of establishing a reproducible mouse model of glaucoma after KPro surgery, specifically that of a miniaturized mouse model of KPro (mKPro). In the present study, a total of 20 corneas of donor C57BL/6 mice (n = 10) were implanted in one eye of each recipient BALB/C mouse (n = 20), assembled as part of the mKPro, either with or without intraoperative lensectomy. Main feasibility outcomes consisted in incidence rates of loss of tone, capsule nicking, and lens extrusion, as well as acquisition of posterior segment optical coherence tomography (OCT) images. With lensectomy (n = 10), loss of ocular tone and retinal detachment occurred in 100% of mice. Without lensectomy (n = 10), capsule nicking and opening, as well as lens extrusion, occurred in 80% of mice. Causes of these complications included the large proportion of intraocular volume occupied by the lens, the shallow anterior chamber, and thus the lack of available intraocular volume to implant the KPro if the lens remains present. Successful mouse KPro surgery may require a great deal of practice to be useful as a reproducible model. Animal KPro models ought to be pursued further by research teams in future studies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据