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首页> 外文期刊>Molecules >Neuroprotective Effects of Methyl 3,4-Dihydroxybenzoate against TBHP-Induced Oxidative Damage in SH-SY5Y Cells
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Neuroprotective Effects of Methyl 3,4-Dihydroxybenzoate against TBHP-Induced Oxidative Damage in SH-SY5Y Cells

机译:3,4-二羟基苯甲酸甲酯对TBHP诱导的SH-SY5Y细胞氧化损伤的神经保护作用

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摘要

This study investigated the neuroprotective effects of methyl 3,4-dihydroxybenzoate (MDHB) against t-butyl hydroperoxide (TBHP) induced oxidative damage in SH-SY5Y (human neuroblastoma cells) and the underlying mechanisms. SH-SY5Y were cultured in DMEM + 10% FBS for 24 h and pretreated with different concentrations of MDHB or N-acetyl-L-cysteine (NAC) for 4 h prior to the addition of 40 mu M TBHP for 24 h. Cell viability was analyzed using the methylthiazolyltetrazolium (MTT) and lactate dehydrogenase (LDH) assays. An annexin V-FITC assay was used to detect cell apoptosis rates. The 2',7'-dichlorofluorescin diacetate (DCFH-DA) assay was used to determine intracellular ROS levels. The activities of antioxidative enzymes (GSH-Px and SOD) were measured using commercially available kits. The oxidative DNA damage marker 8-OHdG was detected using ELISA. Western blotting was used to determine the expression of Bcl-2, Bax, caspase 3, p-Akt and Akt proteins in treated SH-SY5Y cells. Our results showed that MDHB is an effective neuroprotective compound that can mitigate oxidative stress and inhibit apoptosis in SH-SY5Y cells.
机译:这项研究调查了3,4-二羟基苯甲酸甲酯(MDHB)对叔丁基氢过氧化物(TBHP)诱导的SH-SY5Y(人类神经母细胞瘤细胞)氧化损伤的神经保护作用及其潜在机制。 SH-SY5Y在DMEM + 10%FBS中培养24小时,并在加入40μMTBHP 24小时之前,先用不同浓度的MDHB或N-乙酰-L-半胱氨酸(NAC)预处理4小时。使用甲基噻唑基四唑(MTT)和乳酸脱氢酶(LDH)分析来分析细胞活力。膜联蛋白V-FITC测定用于检测细胞凋亡率。 2',7'-二氯二氟荧光素二乙酸酯(DCFH-DA)测定法用于确定细胞内ROS水平。使用市售试剂盒测量抗氧化酶(GSH-Px和SOD)的活性。使用ELISA检测氧化性DNA损伤标记物8-OHdG。使用蛋白质印迹法确定Bcl-2,Bax,胱天蛋白酶3,p-Akt和Akt蛋白在处理过的SH-SY5Y细胞中的表达。我们的结果表明,MDHB是一种有效的神经保护性化合物,可以减轻氧化应激并抑制SH-SY5Y细胞的凋亡。

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