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首页> 外文期刊>Biological & pharmaceutical bulletin >Inhibition of production of reactive oxygen species and gene expression profile by treatment of ethanol extract of moutan cortex radicis in oxidative stressed PC12 cells.
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Inhibition of production of reactive oxygen species and gene expression profile by treatment of ethanol extract of moutan cortex radicis in oxidative stressed PC12 cells.

机译:通过在氧化应激的PC12细胞中处理牡丹皮的乙醇提取物来抑制活性氧的产生和基因表达谱。

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摘要

Moutan Cortex Radicis (MCR) is one of the most widely used Oriental medicines. In this study, we assessed the reducing effect of ethanol extract of MCR on hydrogen peroxide-induced reactive oxygen production, the main cause of cell damage or death in PC12 cells. The viability of cells treated with 1 mg/ml of MCR was significantly restored from that of oxidative-stressed PC12 cells. Measurement of intracellular reactive oxygen species (ROS) generation was determined using the H(2)DCFDA assay. MCR at 1-0.01 mg/ml concentration inhibited ROS production in oxidative-stressed cells. To identify candidate genes responsible for the anti-oxidative effects of MCR on PC12 cells, an oligonucleotide microarray analysis was performed. The result of gene expression profiles showed that 10 genes were up-regulated and 7 were down-regulated in MCR plus hydrogen peroxide treated cells compared with hydrogen peroxide treated cells. Among them, heme oxygenase (HO) and cathechol-O-methyltransferase (COMT) are related to regulation of ROS generation and the others are known to regulate cell survival and progression. Subsequently, we performed real-time RT-PCR to quantify the ROS related gene. MCR treatment increased the expression of HO by 370% and COMT by 280% at the concentration of 1 mg/ml. These findings suggest that MCR inhibits the production of ROS and cytotoxicity by oxidative-stressed PC12 cells through over-expression of HO and COMT.
机译:牡丹皮根癌(MCR)是最广泛使用的东方药物之一。在这项研究中,我们评估了MCR乙醇提取物对过氧化氢诱导的活性氧产生的减少作用,这是造成PC12细胞损伤或死亡的主要原因。用1 mg / ml MCR处理的细胞的活力已从氧化应激的PC12细胞中明显恢复。使用H(2)DCFDA分析确定细胞内活性氧(ROS)生成的测量。 1-0.01 mg / ml浓度的MCR可以抑制氧化应激细胞中的ROS产生。为了鉴定负责MCR对PC12细胞抗氧化作用的候选基因,进行了寡核苷酸微阵列分析。基因表达谱的结果表明,与过氧化氢处理的细胞相比,MCR加过氧化氢处理的细胞中有10个基因被上调,而七个基因被下调。其中,血红素加氧酶(HO)和儿茶酚-O-甲基转移酶(COMT)与ROS的产生有关,而其他已知的物质则可调节细胞的存活和进程。随后,我们进行了实时RT-PCR定量ROS相关基因。在1 mg / ml的浓度下,MCR处理使HO的表达增加370%,COMT的表达增加280%。这些发现表明,MCR通过HO和COMT的过表达来抑制氧化应激的PC12细胞产生ROS和细胞毒性。

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