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二十烷对谷氨酸和N-甲基-D-天冬氨酸诱导的视网膜神经节细胞损伤的神经保护和抗炎作用。

Neuroprotective and anti-inflammatory effects of eicosane on glutamate and NMDA-induced retinal ganglion cell injury.

作者信息

Wu Zhen-Kai, Li Huan-Yu, Zhu You-Lin, Xiong Meng-Qin, Zhong Jing-Xiang

机构信息

Department of Ophthalmology, the First Affiliated Hospital of Jinan University, Guangzhou 510632, Guangdong Province, China.

Changde Hospital, Xiangya School of Medicine, Central South University (the First People's Hospital of Changde City), Changde 415000, Hunan Province, China.

出版信息

Int J Ophthalmol. 2024 Apr 18;17(4):638-645. doi: 10.18240/ijo.2024.04.05. eCollection 2024.

Abstract

AIM

To investigate the protective effects, antioxidant potential, and anti-inflammatory mechanisms of eicosane on glutamate-induced cell damage and on N-methyl-D-aspartate (NMDA)-induced retinal ganglion cell (RGC) injury in a mouse model of glaucoma.

METHODS

The protective effects of eicosane on the rat R28 retinal precursor cell line were assessed using cell counting kit-8 assays and Hoechst-propidium iodide staining. Intracellular reactive oxygen species (ROS) production was measured using the fluorescent probe 2'-7'-dichlorofluorescin diacetate and flow cytometry. The protective role of eicosane on NMDA-induced RGC injury in a mouse glaucoma model was determined by immunostaining of frozen sections of retina. The effects of eicosane on the metabolome of the retina in mice with NMDA-induced RGC damage were evaluated by liquid chromatography-mass spectroscopy (LC-MS) and untargeted metabolomics analyses.

RESULTS

Eicosane treatment significantly attenuated glutamate-induced damage to R28 cells . Eicosane also protected RGCs against NMDA-induced injury in a mouse glaucoma model. Untargeted metabolomics analyses showed that eicosane increased multiple metabolites, including L-arginine and L-carnitine, in the retina.

CONCLUSION

Eicosane has protective effects, antioxidant potential, and anti-inflammatory properties in an model of glutamate-induced cell damage and in an model of NMDA-induced RGC injury in mouse glaucoma through modulation of L-arginine and/or L-carnitine metabolism.

摘要

目的

在青光眼小鼠模型中,研究二十烷对谷氨酸诱导的细胞损伤以及对N-甲基-D-天冬氨酸(NMDA)诱导的视网膜神经节细胞(RGC)损伤的保护作用、抗氧化潜力及抗炎机制。

方法

使用细胞计数试剂盒-8检测法和Hoechst-碘化丙啶染色评估二十烷对大鼠R28视网膜前体细胞系的保护作用。使用荧光探针2'-7'-二氯荧光素二乙酸酯和流式细胞术测量细胞内活性氧(ROS)的产生。通过对视网膜冰冻切片进行免疫染色,确定二十烷对小鼠青光眼模型中NMDA诱导的RGC损伤的保护作用。通过液相色谱-质谱联用(LC-MS)和非靶向代谢组学分析,评估二十烷对NMDA诱导的RGC损伤小鼠视网膜代谢组的影响。

结果

二十烷处理显著减轻了谷氨酸对R28细胞的损伤。二十烷还在小鼠青光眼模型中保护RGC免受NMDA诱导的损伤。非靶向代谢组学分析表明,二十烷增加了视网膜中的多种代谢物,包括L-精氨酸和L-肉碱。

结论

在谷氨酸诱导的细胞损伤模型以及小鼠青光眼NMDA诱导的RGC损伤模型中,二十烷通过调节L-精氨酸和/或L-肉碱代谢,具有保护作用、抗氧化潜力及抗炎特性。

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