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Coenzyme Q10 instilled as eye drops on the cornea reaches the retina and udprotects retinal layers from apoptosis in a mouse model of kainate-induced udretinal damage

机译:辅酶Q10滴眼液滴入角膜到达视网膜和 ud在海藻酸盐诱导的 ud小鼠模型中保护视网膜层免受凋亡视网膜损伤

摘要

Purpose. To evaluate if coenzyme Q10 (CoQ10) can protect retinal ganglion cells (RGCs) from apoptosis and, when instilled as eye drops on the cornea, if it can reach the retina and exert its antiapoptotic activity in this area in a mouse model of kainate (KA)-induced retinal damage. Methods. Rat primary or cultured retinal ganglion cells (RGCs) were subjected to glutamate (50 µM) or chemical hypoxia (Antimycin A 200 µM) or serum withdrawal (FBS 0.5%) in the presence or absence of CoQ10 (10 µM). Cell viability was evaluated by light microscopy and FACS analyses. Apoptosis was evaluated by caspase 3/7 activity and mitochondrion depolarization TMRE analysis. CoQ10 transfer to the retina following its instillation as eye drops on the cornea was quantified by HPLC. Retinal protection by CoQ10 (10 µM) eye drops instilled on the cornea was then evaluated in a mouse model of KA-induced excitotoxic retinal cell apoptosis by cleaved caspase 3 immunohistofluorescence, caspase 3/7 activity assays and quantification of inhibition of RGC loss. Results. CoQ10 significantly increased viable cells by preventing RGC apoptosis. Furthermore, when topically applied as eye drops to the cornea, it reached the retina, thus substantially increasing local CoQ10 concentration and protecting retinal layers from apoptosis. Conclusions. The ability of CoQ10 eye drops to protect retinal cells from apoptosis in the mouse model of KA-induced retinal damage suggests that topical CoQ10 may be evaluated in designing therapies for treating apoptosis-driven retinopathies.
机译:目的。为了评估辅酶Q10(CoQ10)是否可以保护视网膜神经节细胞(RGC)免受凋亡,当滴眼液滴眼液时,它是否可以到达视网膜并在该区域的海藻酸盐小鼠模型中发挥抗凋亡活性( KA)引起的视网膜损伤。方法。在有或没有辅酶Q10(10 µM)的情况下,对大鼠原代或培养的视网膜神经节细胞(RGC)进行谷氨酸(50 µM)或化学低氧(Antimycin A 200 µM)或血清戒断(FBS 0.5%)。通过光学显微镜和FACS分析评估细胞活力。通过半胱天冬酶3/7活性和线粒体去极化TMRE分析评估细胞凋亡。辅酶Q10滴注后,通过HPLC定量测定角膜上的滴眼液,从而将其转移至视网膜。然后通过裂解的胱天蛋白酶3免疫组织荧光,胱天蛋白酶3/7活性测定和定量RGC损失的抑制作用,在KA诱导的兴奋性毒性视网膜细胞凋亡的小鼠模型中评估了滴入角膜的CoQ10(10 µM)滴眼液对视网膜的保护作用。结果。辅酶Q10通过阻止RGC凋亡来显着增加活细胞。此外,当以滴眼剂的形式局部应用到角膜时,它到达了视网膜,从而大大增加了局部CoQ10的浓度并保护了视网膜层免于细胞凋亡。结论。在KA诱导的视网膜损伤的小鼠模型中,CoQ10滴眼液保护视网膜细胞免于凋亡的能力表明,可以在设计用于治疗细胞凋亡驱动的视网膜病变的疗法时评估局部CoQ10。

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