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The novel antioxidant SkQ1 as an effective protector of rat eye tissues during long-term organotypic cultivation

机译:新型抗氧化剂SKQ1作为长期有机型栽培中大鼠眼组织的有效保护器

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Cells possess an array of antioxidant mechanisms for cleaning harmful oxidants and reactive oxygen species (ROS), in particular. Despite of this, ROS overproduction induced mainly by light can cause serious damage to the neural retina (NR) and retinal pigment epithelium (RPE) of the eye that finally leads to different retinal pathologies. Among numerous sites of ROS generation in the cell, mitochondrial electron transport is of crucial importance. Recently the novel penetrating cation 10-(6'-plastoquinonyl) decyltriphenylphosphonium was invented [1]. This cation, designated SkQ1, has a remarkable ability to clean the matrix of mitochondria, "the dirtiest place in the cell" in respect of ROS. It has been demonstrated to possess a powerful antioxidant activity in a number of various in vitro and in vivo models. In particular, a strong protective action of SkQ1 has been revealed upon eye tissues of the adult rat [2]. To develop this finding, we describe here the effects of SkQ1 upon morphology and cell viability in the posterior sector of rat eye, including the complex "RPE-choroid-sclera" isolated with or without NR. We found that under conditions of long-term organotypic 3D cultivation [3], 20 nM SkQ1 significantly conserved the native structure of eye tissues and protein expression in their specific cell types. SkQ1 reduced also cell death, prevented RPE sheet from cell withdrawal and RPE cell phenotype changes, and suppressed transmigration of choroidal cells.
机译:细胞具有用于清洁有害氧化剂和活性氧(ROS)的抗氧化机构阵列。尽管如此,主要用光引起的ROS过产会导致眼睛的神经视网膜(NR)和视网膜色素上皮(RPE)造成严重损害,最终导致不同的视网膜病理学。在细胞中众多ROS的遗址中,线粒体电子传输至关重要。最近,本发明的渗透阳离子10-(6'-塑料醌基)甲基硫氨基鏻是发明[1]。这个阳离子指定SKQ1,具有显着清洁线粒体矩阵的能力,在ROS方面清洁线粒体的基质“最肮脏的地方”。已经证明,在多种体外和体内模型中具有强大的抗氧化活性。特别是,在成年大鼠的眼组织中揭示了SKQ1的强保护作用[2]。为了开发这种发现,我们描述了SKQ1在大鼠眼后部和细胞活力上的影响,包括复杂的“RPE-Choroid-scla”,分离出或没有NR。我们发现,在长期有机型3D栽培条件下,20nm SkQ1显着保守了其特定细胞类型中眼组织和蛋白质表达的天然结构。 SKQ1还减少了细胞死亡,防止来自细胞戒断的RPE表和RPE细胞表型变化,并抑制了脉络细胞的迁移。

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