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Neuroprotective Effects of Citicoline in in Vitro Models of Retinal Neurodegeneration

机译:Citicoline在视网膜神经变性体外模型中的神经保护作用。

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摘要

In recent years, citicoline has been the object of remarkable interest as a possible neuroprotectant. The aim of this study was to investigate if citicoline affected cell survival in primary retinal cultures and if it exerted neuroprotective activity in conditions modeling retinal neurodegeneration. Primary retinal cultures, obtained from rat embryos, were first treated with increasing concentrations of citicoline (up to 1000 μM) and analyzed in terms of apoptosis and caspase activation and characterized by immunocytochemistry to identify neuronal and glial cells. Subsequently, excitotoxic concentration of glutamate or High Glucose-containing cell culture medium (HG) was administered as well-known conditions modeling neurodegeneration. Glutamate or HG treatments were performed in the presence or not of citicoline. Neuronal degeneration was evaluated in terms of apoptosis and loss of synapses. The results showed that citicoline did not cause any damage to the retinal neuroglial population up to 1000 μM. At the concentration of 100 μM, it was able to counteract neuronal cell damage both in glutamate- and HG-treated retinal cultures by decreasing proapoptotic effects and contrasting synapse loss. These data confirm that citicoline can efficiently exert a neuroprotective activity. In addition, the results suggest that primary retinal cultures, under conditions inducing neurodegeneration, may represent a useful system to investigate citicoline neuroprotective mechanisms.
机译:近年来,胞磷胆碱作为一种可能的神经保护剂已引起人们的极大关注。这项研究的目的是调查胞磷胆碱是否会影响原代视网膜培养物中的细胞存活,以及是否在模拟视网膜神经变性的条件下发挥了神经保护作用。首先用递增浓度的胞磷胆碱(最高1000μM)处理从大鼠胚胎获得的原代视网膜培养物,并根据凋亡和胱天蛋白酶激活进行分析,并通过免疫细胞化学进行鉴定,以鉴定神经元和神经胶质细胞。随后,给予兴奋性浓度的谷氨酸或含高葡萄糖的细胞培养基(HG)作为模拟神经变性的众所周知的条件。在或不存在胞磷胆碱的情况下进行谷氨酸或HG处理。根据细胞凋亡和突触损失评估神经元变性。结果表明,胞磷胆碱对高达1000μM的视网膜神经胶质细胞群没有造成任何损害。在浓度为100μM时,它能够通过降低促凋亡作用和对比突触损失来抵消谷氨酸和HG处理的视网膜培养物中神经元细胞的损伤。这些数据证实胞磷胆碱可以有效地发挥神经保护活性。此外,结果表明,在诱导神经退行性变的条件下,原代视网膜培养可能是研究胞磷胆碱神经保护机制的有用系统。

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