Suppr超能文献

年龄相关性黄斑变性中的氧化应激和亚硝化应激:对其在疾病不同阶段作用的综述

Oxidative and Nitrosative Stress in Age-Related Macular Degeneration: A Review of Their Role in Different Stages of Disease.

作者信息

Toma Caterina, De Cillà Stefano, Palumbo Aurelio, Garhwal Divya Praveen, Grossini Elena

机构信息

Eye Clinic, University Hospital Maggiore Della Carità, 28100 Novara, Italy.

Department of Health Sciences, University East Piedmont "A. Avogadro", 28100 Novara, Italy.

出版信息

Antioxidants (Basel). 2021 Apr 23;10(5):653. doi: 10.3390/antiox10050653.

Abstract

Although the exact pathogenetic mechanisms leading to age-related macular degeneration (AMD) have not been clearly identified, oxidative damage in the retina and choroid due to an imbalance between local oxidants/anti-oxidant systems leading to chronic inflammation could represent the trigger event. Different in vitro and in vivo models have demonstrated the involvement of reactive oxygen species generated in a highly oxidative environment in the development of drusen and retinal pigment epithelium (RPE) changes in the initial pathologic processes of AMD; moreover, recent evidence has highlighted the possible association of oxidative stress and neovascular AMD. Nitric oxide (NO), which is known to play a key role in retinal physiological processes and in the regulation of choroidal blood flow, under pathologic conditions could lead to RPE/photoreceptor degeneration due to the generation of peroxynitrite, a potentially cytotoxic tyrosine-nitrating molecule. Furthermore, the altered expression of the different isoforms of NO synthases could be involved in choroidal microvascular changes leading to neovascularization. The purpose of this review was to investigate the different pathways activated by oxidative/nitrosative stress in the pathogenesis of AMD, focusing on the mechanisms leading to neovascularization and on the possible protective role of anti-vascular endothelial growth factor agents in this context.

摘要

尽管导致年龄相关性黄斑变性(AMD)的确切发病机制尚未明确,但局部氧化剂/抗氧化剂系统失衡导致视网膜和脉络膜发生氧化损伤,进而引发慢性炎症,这可能是触发事件。不同的体外和体内模型已证明,在高度氧化环境中产生的活性氧参与了玻璃膜疣的形成以及AMD初始病理过程中视网膜色素上皮(RPE)的变化;此外,最近的证据突出了氧化应激与新生血管性AMD之间可能存在的关联。一氧化氮(NO)在视网膜生理过程和脉络膜血流调节中起关键作用,在病理条件下,由于过氧亚硝酸盐(一种潜在的细胞毒性酪氨酸硝化分子)的产生,可导致RPE/光感受器变性。此外,一氧化氮合酶不同同工型的表达改变可能与导致新生血管形成的脉络膜微血管变化有关。本综述的目的是研究氧化/亚硝化应激在AMD发病机制中激活的不同途径,重点关注导致新生血管形成的机制以及抗血管内皮生长因子药物在此背景下可能的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2400/8145578/a0b3b5c05522/antioxidants-10-00653-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验