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N-acetylcysteine protects Chinese Hamster ovary cells from oxidative injury and apoptosis induced by microcystin-LR

机译:N-乙酰半胱氨酸保护中国仓鼠卵巢细胞免受微囊藻毒素-LR诱导的氧化损伤和细胞凋亡

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摘要

This study aimed to investigate the MC-LR induced oxidative injury and apoptosis in Chinese hamster ovary (CHO) cells, and the protective effects of N-acetylcysteine (NAC) on these cells. Cell viability was determined by MTT assay after exposure to NAC at various concentrations (0, 1, 5, 10, 20, 30, 40, 50, 60 and 80 mmol/L) alone, or NAC (0, 1 and 5 mmol/L) plus MC-LR (0, 2.5, 5 and 10 μg/ml) for 24 h. The reactive oxygen species (ROS) in CHO cells were measured by DCFH-DA, mitochondrial membrane potential (MMP) by fluorescence probe JC-1 staining, and apoptosis index determined by Annexin V-PI staining. Results showed, following exposure to NAC alone for 24 h, cell viability remains higher than 80% at 1 and 5 mmol/L. After exposure to NAC at different concentrations plus MC-LR, cell viability increased, ROS decreased, MMP elevated, and apoptosis index reduced to a certain extent. In conclusion, MC-LR may induce the apoptosis of CHO cells by inducing ROS production which is protected by NAC.
机译:本研究旨在研究MC-LR诱导的中国仓鼠卵巢(CHO)细胞的氧化损伤和凋亡,以及N-乙酰半胱氨酸(NAC)对这些细胞的保护作用。分别以各种浓度(0、1、5、10、20、30、40、50、60和80 mmol / L)或NAC(0、1、5和5 mmol / L)暴露于NAC后,通过MTT分析测定细胞活力L)加MC-LR(0、2.5、5和10μg/ ml)24小时。用DCFH-DA测定CHO细胞中的活性氧(ROS),用荧光探针JC-1染色测定线粒体膜电位(MMP),用Annexin V-PI染色测定细胞凋亡指数。结果显示,仅暴露于NAC 24小时后,细胞活力在1和5 mmol / L时仍高于80%。暴露于不同浓度的NAC加MC-LR后,细胞活力有所提高,ROS降低,MMP升高,并且凋亡指数有所降低。总之,MC-LR可能通过诱导受NAC保护的ROS产生来诱导CHO细胞凋亡。

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