Biophytis, Sorbonne Université-BC9, 4 Place Jussieu, 75005 Paris, France.
Sorbonne Université, CNRS-Institut de Biologie Paris Seine (BIOSIPE), 75005 Paris, France.
Oxid Med Cell Longev. 2020 Dec 8;2020:4984927. doi: 10.1155/2020/4984927. eCollection 2020.
Age-related macular degeneration (AMD) is the commonest cause of severe visual loss and blindness in developed countries among individuals aged 60 and older. AMD slowly progresses from early AMD to intermediate AMD (iAMD) and ultimately late-stage AMD. Late AMD encompasses either neovascular AMD (nAMD) or geographic atrophy (GA). nAMD is defined by choroidal neovascularization (CNV) and hemorrhage in the subretinal space at the level of the macula. This induces a rapid visual impairment caused by the death of photoreceptor cells. Intravitreal injection of anti-vascular endothelial growth factor (VEGF) antibodies is the standard treatment of nAMD but adds to the burden of patient care. GA is characterized by slowly expanding photoreceptor, and retinal pigment epithelium (RPE) degeneration patches progressively leading to blindness. There is currently no therapy to cure GA. Late AMD continues to be an unmet medical need representing a major health problem with millions of patients worldwide. Oxidative stress and inflammation are recognized as some of the main risk factors to developing late AMD. The antioxidant formulation AREDS (Age-Related Eye Disease Studies), contains -carotene, which has been replaced by lutein and zeaxanthin in AREDS2, are given to patients with iAMD but have a limited effect on the incidence of nAMD and GA. Thus, to avoid or slowdown the development of late stages of AMD (nAMD or GA), new therapies targeting iAMD are needed such as crocetin obtained through hydrolysis of crocin, an important component of saffron (.), and norbixin derived from bixin extracted from seeds. We have shown that these apocarotenoids preserved more effectively RPE cells against apoptosis following blue light exposure in the presence of A2E than lutein and zeaxanthin. In this review, we will discuss the potential use of apocarotenoids to slowdown the progression of iAMD, to reduce the incidence of both forms of late AMD.
年龄相关性黄斑变性(AMD)是发达国家 60 岁及以上人群中导致严重视力丧失和失明的最常见原因。AMD 从早期 AMD 缓慢进展为中期 AMD(iAMD),最终发展为晚期 AMD。晚期 AMD 包括新生血管性 AMD(nAMD)或地理萎缩(GA)。nAMD 定义为脉络膜新生血管(CNV)和黄斑水平的视网膜下空间出血。这会导致光感受器细胞死亡引起的快速视力损害。抗血管内皮生长因子(VEGF)抗体的玻璃体内注射是 nAMD 的标准治疗方法,但会增加患者护理的负担。GA 的特征是感光器和视网膜色素上皮(RPE)逐渐扩大变性斑块,最终导致失明。目前尚无治愈 GA 的方法。晚期 AMD 仍然是一个未满足的医疗需求,代表着全球数百万人的主要健康问题。氧化应激和炎症被认为是导致晚期 AMD 的一些主要危险因素。抗氧化配方 AREDS(年龄相关性眼病研究)含有β-胡萝卜素,在 AREDS2 中已被叶黄素和玉米黄质取代,用于 iAMD 患者,但对 nAMD 和 GA 的发病率影响有限。因此,为了避免或减缓晚期 AMD(nAMD 或 GA)的发展,需要针对 iAMD 的新疗法,例如通过水解藏红花中的主要成分藏红花酸获得的西红花酸 crocetin 和从 种子中提取的二酮玉米黄质 norbixin。我们已经表明,这些类胡萝卜素在存在 A2E 的情况下,比叶黄素和玉米黄质更有效地保存 RPE 细胞免受蓝光照射引起的细胞凋亡。在这篇综述中,我们将讨论类胡萝卜素在减缓 iAMD 进展、降低两种形式的晚期 AMD 发病率方面的潜在用途。