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氧化应激在年龄相关性黄斑变性中的核心作用:来自分子机制和动物模型综述的证据。

Central Role of Oxidative Stress in Age-Related Macular Degeneration: Evidence from a Review of the Molecular Mechanisms and Animal Models.

机构信息

School of Optometry, The Hong Kong Polytechnic University, Hong Kong.

Department of Optometry, University of Cape Coast, Ghana.

出版信息

Oxid Med Cell Longev. 2020 Feb 10;2020:7901270. doi: 10.1155/2020/7901270. eCollection 2020.

Abstract

Age-related macular degeneration (AMD) is a common cause of visual impairment in the elderly. There are very limited therapeutic options for AMD with the predominant therapies targeting vascular endothelial growth factor (VEGF) in the retina of patients afflicted with wet AMD. Hence, it is important to remind readers, especially those interested in AMD, about current studies that may help to develop novel therapies for other stages of AMD. This study, therefore, provides a comprehensive review of studies on human specimens as well as rodent models of the disease, to identify and analyze the molecular mechanisms behind AMD development and progression. The evaluation of this information highlights the central role that oxidative damage in the retina plays in contributing to major pathways, including inflammation and angiogenesis, found in the AMD phenotype. Following on the debate of oxidative stress as the earliest injury in the AMD pathogenesis, we demonstrated how the targeting of oxidative stress-associated pathways, such as autophagy and nuclear factor erythroid 2-related factor 2 (Nrf2) signaling, might be the futuristic direction to explore in the search of an effective treatment for AMD, as the dysregulation of these mechanisms is crucial to oxidative injury in the retina. In addition, animal models of AMD have been discussed in great detail, with their strengths and pitfalls included, to assist inform in the selection of suitable models for investigating any of the molecular mechanisms.

摘要

年龄相关性黄斑变性(AMD)是老年人视力损害的常见原因。AMD 患者的视网膜中血管内皮生长因子(VEGF)是主要的治疗靶点,而 AMD 的治疗选择非常有限。因此,提醒读者,特别是对 AMD 感兴趣的读者,关注可能有助于开发其他阶段 AMD 新疗法的当前研究非常重要。因此,本研究对人类标本和疾病的啮齿动物模型进行了全面综述,以确定和分析 AMD 发展和进展背后的分子机制。对这些信息的评估突出了视网膜中的氧化损伤在促进包括炎症和血管生成在内的主要途径中所起的核心作用,这些途径在 AMD 表型中发现。继氧化应激作为 AMD 发病机制中最早的损伤的争论之后,我们展示了如何针对氧化应激相关途径,如自噬和核因子红细胞 2 相关因子 2(Nrf2)信号通路,这可能是未来探索 AMD 有效治疗方法的方向,因为这些机制的失调对视网膜中的氧化损伤至关重要。此外,还详细讨论了 AMD 的动物模型,包括它们的优缺点,以帮助选择合适的模型来研究任何分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a667/7035553/cf9f495f4803/OMCL2020-7901270.001.jpg

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