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首页> 外文期刊>Metabolic brain disease >Protective effects of alpha lipoic acid on high glucose-induced neurotoxicity in PC12 cells
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Protective effects of alpha lipoic acid on high glucose-induced neurotoxicity in PC12 cells

机译:α硫辛酸对高糖诱导的PC12细胞神经毒性的保护作用

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Hyperglycemia plays an important role in the development of diabetic neuropathy. In this study, we investigated the protective effects of alpha lipoic acid (ALA) against high glucose-induced neurotoxicity in PC12 cells as a suitable in vitro model for studying neuronal functions. PC12 cells were treated with high glucose (25 mg/ml for 24 h) in the absence and presence of ALA (100 mu M for 24 h). The viability of PC12 cells was estimated by using MTT assay. The expression of pro- apoptotic Bax, anti- apoptotic Bcl-2 and caspase 3 protein were evaluated by western blotting. The reactive oxygen species (ROS) levels were determined with 2,7-dichlorodihydro- fluorescein diacetate (H(2)DCFDA). Biochemical markers of oxidative stress were assessed by using the total antioxidant power (TAP), lipid peroxidation (LPO), ADP/ATP ratio, activity of antioxidant enzymes catalase (CAT) and superoxide dismutase (SOD). Pretreatment of PC12 cells with ALA, significantly improved high glucose-induced toxicity by increasing activity of antioxidant enzymes CAT and SOD in the PC12 cell. It also increased the concentrations of TAP. An elevated level of cell death and ROS in high glucose conditions, diminished with ALA treatment. Over expression of Bax and caspase 3 protein, elevation of ADP/ATP ratio and LPO level in high glucose- treated PC12 cells, were significantly reduced by ALA. It was concluded that ALA attenuates neurotoxicity induced by high glucose in PC12 cells.
机译:高血糖症在糖尿病性神经病的发展中起重要作用。在这项研究中,我们调查了α硫辛酸(ALA)对PC12细胞中高葡萄糖诱导的神经毒性的保护作用,作为研究神经元功能的体外模型。在不存在和存在ALA(100μM,24小时)的情况下,用高葡萄糖(25 mg / ml,24小时)处理PC12细胞。通过使用MTT测定法评估PC12细胞的生存力。通过蛋白质印迹法评估凋亡前Bax,抗凋亡Bcl-2和caspase 3蛋白的表达。用2,7-二氯二氢荧光素二乙酸酯(H(2)DCFDA)测定活性氧(ROS)的水平。通过使用总抗氧化能力(TAP),脂质过氧化(LPO),ADP / ATP比,抗氧化酶过氧化氢酶(CAT)和超氧化物歧化酶(SOD)的活性来评估氧化应激的生化指标。用ALA预处理PC12细胞,可通过增加PC12细胞中抗氧化酶CAT和SOD的活性来显着改善高糖诱导的毒性。它还增加了TAP的浓度。在高葡萄糖条件下,细胞死亡和ROS升高的水平,通过ALA治疗可以降低。 Bax和caspase 3蛋白的过度表达,高糖处理的PC12细胞中ADP / ATP比和LPO水平的升高被ALA显着降低。结论是,ALA减弱了PC12细胞中高葡萄糖诱导的神经毒性。

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