Moine Espérance, Brabet Philippe, Guillou Laurent, Durand Thierry, Vercauteren Joseph, Crauste Céline
Institute of Biomolecules Max Mousseron (IBMM), UMR 5247-CNRS-UM-ENSCM, Faculty of Pharmacy, 15 av. Charles Flahault, 34093 Montpellier, France.
Institute for Neurosciences of Montpellier, INSERM U1051-UM, Hospital St Eloi, 80 rue Augustin Fliche, 34091 Montpellier, France.
Antioxidants (Basel). 2018 Dec 19;7(12):197. doi: 10.3390/antiox7120197.
Age-related macular degeneration (AMD) is a multifactorial pathology and its progression is exacerbated by oxidative stress. Oxidation and photo-oxidation reactions modify lipids in retinal cells, contribute to tissue injury, and lead to the formation of toxic adducts. In particular, autofluorescent pigments such as -retinylidene--retinylethanolamine (A2E) accumulate as lipofuscin in retinal pigment epithelial cells, contribute to the production of additional reactive oxygen species (ROS), and lead to cell degeneration. In an effort to develop efficient antioxidants to reduce damage caused by lipid oxidation, various natural polyphenols were structurally modified to increase their lipophilicity (lipophenols). In this study, resveratrol, phloroglucinol, quercetin and catechin were selected and conjugated to various polyunsaturated fatty acids (PUFAs) using classical chemical strategies or enzymatic reactions. After screening for cytotoxicity, the capacity of the synthesized lipophenols to reduce ROS production was evaluated in ARPE-19 cells subjected to H₂O₂ treatment using a dichlorofluorescein diacetate probe. The positions of the PUFA on the polyphenol core appear to influence the antioxidant effect. In addition, two lipophenolic quercetin derivatives were evaluated to highlight their potency in protecting ARPE-19 cells against A2E photo-oxidation toxicity. Quercetin conjugated to linoleic or α-linolenic acid were promising lipophilic antioxidants, as they protected ARPE-19 cells from A2E-induced cell death more effectively than the parent polyphenol, quercetin.
年龄相关性黄斑变性(AMD)是一种多因素疾病,氧化应激会加剧其进展。氧化和光氧化反应会改变视网膜细胞中的脂质,导致组织损伤,并形成有毒加合物。特别是,诸如视黄叉视黄基乙醇胺(A2E)之类的自发荧光色素会作为脂褐素在视网膜色素上皮细胞中积累,导致产生更多的活性氧(ROS),并导致细胞变性。为了开发有效的抗氧化剂以减少脂质氧化造成的损害,对各种天然多酚进行了结构修饰以提高其亲脂性(脂多酚)。在本研究中,选择了白藜芦醇、间苯三酚、槲皮素和儿茶素,并使用经典化学策略或酶促反应将它们与各种多不饱和脂肪酸(PUFA)偶联。在筛选细胞毒性后,使用二氯荧光素二乙酸酯探针在经过H₂O₂处理的ARPE-19细胞中评估合成的脂多酚减少ROS产生的能力。PUFA在多酚核心上的位置似乎会影响抗氧化效果。此外,对两种脂酚型槲皮素衍生物进行了评估,以突出它们在保护ARPE-19细胞免受A2E光氧化毒性方面的效力。与亚油酸或α-亚麻酸偶联的槲皮素是很有前景的亲脂性抗氧化剂,因为它们比母体多酚槲皮素更有效地保护ARPE-19细胞免受A2E诱导的细胞死亡。