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本文引用的文献

1
Zeaxanthin and Lutein: Photoprotectors, Anti-Inflammatories, and Brain Food.玉米黄质和叶黄素:光保护剂、抗炎剂和大脑食物。
Molecules. 2020 Aug 8;25(16):3607. doi: 10.3390/molecules25163607.
2
Improvement in inner retinal function in glaucoma with nicotinamide (vitamin B3) supplementation: A crossover randomized clinical trial.尼可酰胺(维生素 B3)补充治疗对青光眼患者内层视网膜功能的改善作用:一项交叉随机临床试验。
Clin Exp Ophthalmol. 2020 Sep;48(7):903-914. doi: 10.1111/ceo.13818. Epub 2020 Jul 28.
3
Retinal energy metabolism in health and glaucoma.健康与青光眼状态下的视网膜能量代谢
Prog Retin Eye Res. 2021 Mar;81:100881. doi: 10.1016/j.preteyeres.2020.100881. Epub 2020 Jul 23.
4
NAD homeostasis in health and disease.NAD 平衡在健康和疾病中的作用。
Nat Metab. 2020 Jan;2(1):9-31. doi: 10.1038/s42255-019-0161-5. Epub 2020 Jan 20.
5
Role of Epithelial-Mesenchymal Transition in Retinal Pigment Epithelium Dysfunction.上皮-间质转化在视网膜色素上皮功能障碍中的作用
Front Cell Dev Biol. 2020 Jun 25;8:501. doi: 10.3389/fcell.2020.00501. eCollection 2020.
6
Neuroprotection: A versatile approach to combat glaucoma.神经保护:一种对抗青光眼的多效方法。
Eur J Pharmacol. 2020 Aug 15;881:173208. doi: 10.1016/j.ejphar.2020.173208. Epub 2020 May 25.
7
Implications of NAD Metabolism in the Aging Retina and Retinal Degeneration.NAD 代谢对衰老视网膜和视网膜变性的影响。
Oxid Med Cell Longev. 2020 May 9;2020:2692794. doi: 10.1155/2020/2692794. eCollection 2020.
8
Improving retinal mitochondrial function as a treatment for age-related macular degeneration.改善视网膜线粒体功能作为治疗年龄相关性黄斑变性的方法。
Redox Biol. 2020 Jul;34:101552. doi: 10.1016/j.redox.2020.101552. Epub 2020 May 18.
9
Altered photoreceptor metabolism in mouse causes late stage age-related macular degeneration-like pathologies.小鼠光感受器代谢改变导致晚期年龄相关性黄斑变性样病变。
Proc Natl Acad Sci U S A. 2020 Jun 9;117(23):13094-13104. doi: 10.1073/pnas.2000339117. Epub 2020 May 20.
10
Vascular permeability in retinopathy is regulated by VEGFR2 Y949 signaling to VE-cadherin.血管通透性在视网膜病变中受 VEGFR2 Y949 信号调节至 VE-钙黏蛋白。
Elife. 2020 Apr 21;9:e54056. doi: 10.7554/eLife.54056.

补充 NAD 对青光眼和年龄相关性黄斑变性的潜在治疗益处。

Potential Therapeutic Benefit of NAD Supplementation for Glaucoma and Age-Related Macular Degeneration.

机构信息

Department of Clinical Neuroscience, Division of Eye and Vision, St. Erik Eye Hospital, Karolinska Institutet, 112 82 Stockholm, Sweden.

School of Optometry and Vision Sciences, Cardiff University, Cardiff CF24 4HQ, Wales, UK.

出版信息

Nutrients. 2020 Sep 19;12(9):2871. doi: 10.3390/nu12092871.

DOI:10.3390/nu12092871
PMID:32961812
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7551676/
Abstract

Glaucoma and age-related macular degeneration are leading causes of irreversible blindness worldwide with significant health and societal burdens. To date, no clinical cures are available and treatments target only the manageable symptoms and risk factors (but do not remediate the underlying pathology of the disease). Both diseases are neurodegenerative in their pathology of the retina and as such many of the events that trigger cell dysfunction, degeneration, and eventual loss are due to mitochondrial dysfunction, inflammation, and oxidative stress. Here, we critically review how a decreased bioavailability of nicotinamide adenine dinucleotide (NAD; a crucial metabolite in healthy and disease states) may underpin many of these aberrant mechanisms. We propose how exogenous sources of NAD may become a therapeutic standard for the treatment of these conditions.

摘要

青光眼和年龄相关性黄斑变性是全球范围内导致不可逆性失明的主要原因,给健康和社会带来了重大负担。迄今为止,尚无临床治愈方法,治疗方法仅针对可管理的症状和风险因素(但不能改善疾病的根本病理)。这两种疾病在视网膜的病理方面都是神经退行性的,因此,许多引发细胞功能障碍、退化和最终丧失的事件都归因于线粒体功能障碍、炎症和氧化应激。在这里,我们批判性地回顾了烟酰胺腺嘌呤二核苷酸(NAD;健康和疾病状态下的关键代谢物)生物利用度的降低如何可能成为许多这些异常机制的基础。我们提出了外源性 NAD 来源如何可能成为治疗这些疾病的治疗标准。