碘酸钠与过氧化脂质治疗老年性黄斑变性小鼠模型药物评价的比较

Soo-Young Kim, Haohua Qian
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引用次数: 0

摘要

目的:本文综述了年龄相关性黄斑变性(AMD)的非转基因模型,重点介绍了碘酸钠和过氧化脂质(HpODE)诱导的小鼠视网膜变性的临床前研究平台。背景:在人口日益老龄化的世界中,AMD是视力丧失的最常见原因。早期和中期黄斑变性的主要表型是黄斑变性和自身荧光增加,神经胶质细胞活化,视网膜下小胶质细胞浸润和视网膜色素上皮细胞向内移动。中度黄斑变性可发展为晚期黄斑变性,以地理性萎缩和/或脉络膜新生血管为特征。各种与视网膜变性相关的转基因和非转基因动物模型被用来研究AMD的发病机制和病理生物学,并被广泛用作潜在的治疗评价平台。方法:建立碘酸钠和高聚羟基戊二醇(HpODE)诱导的小鼠视网膜变性模型。比较了两种模型的病理特点和处理方法。此外,还阐述了实用的方案和材料准备与评估方法。结论:碘酸钠和HpODE引起的小鼠视网膜变性与人AMD的许多临床特征相似,与已有的其他动物模型相吻合。然而,临床前研究需要标准化的程序和评估方案。进一步研究不同途径、剂量和种类的HpODE将对未来的广泛利用有价值。尽管小鼠研究有许多优点,但应始终考虑到小鼠与人之间的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison between sodium iodate and lipid peroxide murine models of age-related macular degeneration for drug evaluation-a narrative review.

Comparison between sodium iodate and lipid peroxide murine models of age-related macular degeneration for drug evaluation-a narrative review.

Comparison between sodium iodate and lipid peroxide murine models of age-related macular degeneration for drug evaluation-a narrative review.

Comparison between sodium iodate and lipid peroxide murine models of age-related macular degeneration for drug evaluation-a narrative review.

Objective: In this review, non-transgenic models of age-related macular degeneration (AMD) are discussed, with focuses on murine retinal degeneration induced by sodium iodate and lipid peroxide (HpODE) as preclinical study platforms.

Background: AMD is the most common cause of vision loss in a world with an increasingly aging population. The major phenotypes of early and intermediate AMD are increased drusen and autofluorescence, Müller glia activation, infiltrated subretinal microglia and inward moving retinal pigment epithelium cells. Intermediate AMD may progress to advanced AMD, characterized by geography atrophy and/or choroidal neovascularization. Various transgenic and non-transgenic animal models related to retinal degeneration have been generated to investigate AMD pathogenesis and pathobiology, and have been widely used as potential therapeutic evaluation platforms.

Methods: Two retinal degeneration murine models induced by sodium iodate and HpODE are described. Distinct pathological features and procedures of these two models are compared. In addition, practical protocol and material preparation and assessment methods are elaborated.

Conclusion: Retina degeneration induced by sodium iodate and HpODE in mouse eye resembles many clinical aspects of human AMD and complimentary to the existent other animal models. However, standardization of procedure and assessment protocols is needed for preclinical studies. Further studies of HpODE on different routes, doses and species will be valuable for the future extensive use. Despite many merits of murine studies, differences between murine and human should be always considered.

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