Discipline of Ophthalmology & Visual Sciences, Level 7 Adelaide Health and Medical Sciences Building, University of Adelaide, North Terrace, Adelaide, SA, 5000, Australia; South Australian Institute of Ophthalmology, Royal Adelaide Hospital, Port Road, SA 5000, Australia.
Discipline of Ophthalmology & Visual Sciences, Level 7 Adelaide Health and Medical Sciences Building, University of Adelaide, North Terrace, Adelaide, SA, 5000, Australia; South Australian Institute of Ophthalmology, Royal Adelaide Hospital, Port Road, SA 5000, Australia.
Exp Eye Res. 2024 Nov;248:110074. doi: 10.1016/j.exer.2024.110074. Epub 2024 Sep 7.
Reactive oxygen species (ROS) play a significant role in toxicity to the retina in a variety of diseases. N-acetylcysteine (NAC), N-acetylcysteine amide (NACA) and the dimeric di-N-acetylcysteine amide (diNACA) were evaluated in terms of protecting retinal cells, in vitro, in a variety of stress models. Three types of rat retinal cell cultures were utilized in the study: macroglial-only cell cultures, neuron-only retinal ganglion cell (RGC) cultures, and mixed cultures containing retinal glia and neurons. Ability of test agents to attenuate oxidative stress in all cultures was ascertained. In addition, capability of agents to protect against a variety of alternate clinically-relevant stressors, including excitotoxins and mitochondrial electron transport chain inhibitors, was also evaluated. Capacity of test agents to elevate cellular levels of reduced glutathione under normal and compromised conditions was also determined. NAC, NACA and diNACA demonstrated concentration-dependent cytoprotection against oxidative stress in all cultures. These three compounds, however, had differing effects against a variety of alternate insults to retinal cells. The most protective agent was NACA, which was most potent against the most stressors (including oxidative stress, mitochondrial impairment by antimycin A and azide, and glutamate-induced excitotoxicity). Similar to NAC, NACA increased glutathione levels in non-injured cells, although diNACA did not, suggesting a different, unknown mechanism of antioxidant activity for the latter. In support of this, diNACA was the only agent to attenuate rotenone-induced toxicity in mitochondria. NAC, NACA and diNACA exhibited varying degrees of antioxidant activity, i.e., protected cultured rat retinal cells from a variety of stressors which were designed to mimic aspects of the pathology of different retinal diseases. A general rank order of activity was observed: NACA ≥ diNACA > NAC. These results warrant further exploration of NACA and diNACA as antioxidant therapeutics for the treatment of retinal diseases, particularly those involving oxidative stress. Furthermore, we have defined the battery of tests carried out as the "Wood, Chidlow, Wall and Casson (WCWC) Retinal Antioxidant Indices"; we believe that these are of great value for screening molecules for potential to reduce retinal oxidative stress in a range of retinal diseases.
活性氧(ROS)在多种疾病对视网膜的毒性中起着重要作用。N-乙酰半胱氨酸(NAC)、N-乙酰半胱氨酸酰胺(NACA)和二聚二-N-乙酰半胱氨酸酰胺(diNACA)在各种应激模型中,从保护视网膜细胞的角度进行了评估。该研究中使用了三种类型的大鼠视网膜细胞培养物:仅胶质细胞培养物、仅神经元视网膜神经节细胞(RGC)培养物以及含有视网膜胶质细胞和神经元的混合培养物。确定了测试剂减轻所有培养物中氧化应激的能力。此外,还评估了这些药剂对各种替代的临床相关应激物(包括兴奋性毒素和线粒体电子传递链抑制剂)的保护能力。还确定了测试剂在正常和受损条件下升高细胞内还原型谷胱甘肽水平的能力。NAC、NACA 和 diNACA 在所有培养物中均表现出对氧化应激的浓度依赖性细胞保护作用。然而,这三种化合物对各种替代的视网膜细胞损伤具有不同的作用。最具保护作用的试剂是 NACA,它对大多数应激物(包括氧化应激、抗霉素 A 和叠氮化物引起的线粒体损伤以及谷氨酸诱导的兴奋性毒性)最有效。与 NAC 相似,NACA 增加了未受伤细胞中的谷胱甘肽水平,而 diNACA 则没有,这表明后者具有一种不同的、未知的抗氧化活性机制。支持这一点的是,diNACA 是唯一能够减轻鱼藤酮引起的线粒体毒性的试剂。NAC、NACA 和 diNACA 表现出不同程度的抗氧化活性,即保护培养的大鼠视网膜细胞免受多种应激物的侵害,这些应激物旨在模拟不同视网膜疾病的病理学方面。观察到活性的一般等级顺序:NACA≥diNACA>NAC。这些结果进一步证明了 NACA 和 diNACA 作为抗氧化治疗剂用于治疗视网膜疾病,特别是涉及氧化应激的疾病的潜力。此外,我们已经确定了进行的一系列测试为“Wood、Chidlow、Wall 和 Casson (WCWC) 视网膜抗氧化指数”;我们相信,这些对于筛选具有在多种视网膜疾病中降低视网膜氧化应激潜力的分子非常有价值。