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年龄相关性黄斑变性中的氧化应激:Nrf2作为治疗靶点

Oxidative Stress in Age-Related Macular Degeneration: Nrf2 as Therapeutic Target.

作者信息

Bellezza Ilaria

机构信息

Department of Experimental Medicine, University of Perugia, Perugia, Italy.

出版信息

Front Pharmacol. 2018 Nov 5;9:1280. doi: 10.3389/fphar.2018.01280. eCollection 2018.

Abstract

Age-related macular degeneration is one of the leading causes of vision loss in the elderly. Genetics, environmental insults, and age-related issues are risk factors for the development of the disease. All these risk factors are linked to the induction of oxidative stress. In young subjects retinal pigment epithelial cells mitigate reactive oxygen generation by the elimination of dysfunctional mitochondria, via mitophagy, and by increasing antioxidant defenses via Nrf2 activation. The high amount of UV light absorbed by the retina, together with cigarette smoking, cooperate with the aging process to increase the amount of reactive oxygen species generated by retinal pigment epithelium where oxidative stress arises. Moreover, in the elderly both the mitophagic process and Nrf2 activation are impaired thus causing retinal cell death. This review will focus on the impact of oxidative stress on the pathogenesis of age-related macular degeneration and analyze the natural and synthetic Nrf2-activating compounds that have been tested as potential therapeutic agents for the disease.

摘要

年龄相关性黄斑变性是老年人视力丧失的主要原因之一。遗传因素、环境损伤和与年龄相关的问题是该疾病发生发展的危险因素。所有这些危险因素都与氧化应激的诱导有关。在年轻个体中,视网膜色素上皮细胞通过线粒体自噬消除功能失调的线粒体,并通过激活Nrf2增加抗氧化防御,从而减轻活性氧的产生。视网膜吸收的大量紫外线与吸烟共同作用,随着衰老过程的进展,增加视网膜色素上皮产生的活性氧的量,进而引发氧化应激。此外,在老年人中,线粒体自噬过程和Nrf2激活均受损,从而导致视网膜细胞死亡。本综述将聚焦于氧化应激对年龄相关性黄斑变性发病机制的影响,并分析已作为该疾病潜在治疗药物进行测试的天然和合成Nrf2激活化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2af/6230566/4b6ef94bb1d7/fphar-09-01280-g001.jpg

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