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注射全身碘酸钠作为扩大性地图状萎缩的模型。

Systemic Sodium Iodate Injection as a Model for Expanding Geographic Atrophy.

作者信息

Anderson Brandon D, Bell Brent A, Song Ying, Lee Timothy T, Wang Tan, Dunaief Joshua L

机构信息

FM Kirby Center for Molecular Ophthalmology, Scheie Eye Institute, Department of Ophthalmology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

出版信息

Transl Vis Sci Technol. 2025 Jan 2;14(1):9. doi: 10.1167/tvst.14.1.9.

Abstract

PURPOSE

Geographic atrophy (GA), an advanced form of dry age-related macular degeneration (AMD), has limited treatment options. This study introduces a novel mouse model featuring an expanding GA patch that can be used to test mechanisms and therapeutics.

METHODS

C57Bl/6J male mice (n = 96) aged 9-10 weeks received an intraperitoneal (IP) injection of 20 mg/kg sodium iodate (NaIO3). In vivo confocal scanning laser ophthalmoscope (cSLO) and optical coherence tomography imaging were done at one, four, eight, and 16 weeks after injection, with GA area measurements taken at weeks 8 and 16. Mice were euthanized on weeks 8 and 16 for histological analysis.

RESULTS

Administration of 20 mg/kg intraperitoneal NaIO3 caused variable damage levels. Approximately 22% of cases showed damage (speckled autofluorescence) covering 35% to 90% of the 102° field of view cSLO image at one week after injection. These mice developed an expanding patch of GA by week 8, with a mean 1.45-fold increase in area by week 16. This region showed complete photoreceptor and retinal pigment epithelium loss and complement activation at the atrophy edge, whereas the inner retina remained undamaged. Mice with less damage (48% of cases) only developed incomplete outer retinal degeneration, and mice with more damage (30% of cases) had too much GA for measurable expansion.

CONCLUSIONS

Although expanding GA formed in only 22% of mice, the model's simplicity and predictability for GA development via one-week post-injection imaging make it suitable for GA therapeutic experimentation.

TRANSLATIONAL RELEVANCE

This murine model provides a valuable tool for testing GA therapies, mirroring clinical endpoints relevant to human trials.

摘要

目的

地图样萎缩(GA)是干性年龄相关性黄斑变性(AMD)的一种晚期形式,其治疗选择有限。本研究引入了一种新型小鼠模型,该模型具有不断扩大的GA斑块,可用于测试发病机制和治疗方法。

方法

9至10周龄的C57Bl/6J雄性小鼠(n = 96)腹腔注射20 mg/kg碘酸钠(NaIO3)。在注射后1周、4周、8周和16周进行体内共聚焦扫描激光检眼镜(cSLO)和光学相干断层扫描成像,并在第8周和第16周测量GA面积。在第8周和第16周对小鼠实施安乐死以进行组织学分析。

结果

腹腔注射20 mg/kg NaIO3造成的损伤程度各不相同。注射后1周,约22%的病例显示损伤(斑点状自发荧光)覆盖了cSLO图像102°视野的35%至90%。这些小鼠到第8周时形成了一个不断扩大的GA斑块,到第16周时面积平均增加了1.45倍。该区域显示光感受器和视网膜色素上皮完全丧失,萎缩边缘有补体激活,而视网膜内层未受损。损伤较轻的小鼠(48%的病例)仅发生不完全性视网膜外层变性,损伤较重的小鼠(30%的病例)GA面积过大,无法测量其扩展情况。

结论

虽然只有22%的小鼠形成了不断扩大的GA,但该模型的简单性以及通过注射后1周成像对GA发展的可预测性使其适用于GA治疗实验。

转化相关性

该小鼠模型为测试GA治疗方法提供了一个有价值的工具,反映了与人体试验相关的临床终点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3e6/11731155/a45763ff0ad6/tvst-14-1-9-f001.jpg

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