首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Proteomic Identification of Nrf2-Mediated Phase II Enzymes Critical for Protection of Tao Hong Si Wu Decoction against Oxygen Glucose Deprivation Injury in PC12 Cells
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Proteomic Identification of Nrf2-Mediated Phase II Enzymes Critical for Protection of Tao Hong Si Wu Decoction against Oxygen Glucose Deprivation Injury in PC12 Cells

机译:Nrf2介导的II期酶的蛋白质组学鉴定对于保护桃红四物汤抗PC12细胞中的氧葡萄糖剥夺损伤至关重要。

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摘要

Chinese herbal medicine formula Tao Hong Si Wu decoction (THSWD) is traditionally used in China for cerebrovascular diseases. However, the molecular mechanisms of THSWD associated with the cerebral ischemia reperfusion injury are largely unknown. The current study applied the two-dimensional gel electrophoresis-based proteomics to investigate the different protein profiles in PC12 cells with and without the treatment of THSWD. Twenty-six proteins affected by THSWD were identified by MALDI-TOF mass spectrometry. Gene ontology analysis showed that those proteins participated in several important biological processes and exhibited diverse molecular functions. In particular, six of them were found to be phase II antioxidant enzymes, which were regulated by NF-E2-related factor-2 (Nrf2). Quantitative PCR further confirmed a dose-dependent induction of the six phase II enzymes by THSWD at the transcription level. Moreover, the individual ingredients of THSWD were discovered to synergistically contribute to the induction of phase II enzymes. Importantly, THSWD's protection against oxygen-glucose deprivation-reperfusion (OGD-Rep) induced cell death was significantly attenuated by antioxidant response element (ARE) decoy oligonucleotides, suggesting the protection of THSWD may be likely regulated at least in part by Nrf2-mediated phase II enzymes. Thus, our data will help to elucidate the molecular mechanisms underlying the neuroprotective effect of THSWD.
机译:中草药配方桃红四物汤(THSWD)在中国传统上用于脑血管疾病。然而,THSWD与脑缺血再灌注损伤相关的分子机制在很大程度上尚不清楚。当前的研究应用了基于二维凝胶电泳的蛋白质组学,研究了有无THSWD处理的PC12细胞中的不同蛋白质谱。通过MALDI-TOF质谱鉴定了受THSWD影响的26种蛋白质。基因本体分析表明,这些蛋白质参与了几个重要的生物学过程,并表现出多种分子功能。特别地,发现其中六种是II期抗氧化剂,受NF-E2相关因子2(Nrf2)调节。定量PCR进一步证实了THSWD在转录水平上对六相II酶的剂量依赖性诱导。此外,已发现THSWD的各个成分协同促进II期酶的诱导。重要的是,THSWD对氧-葡萄糖剥夺-再灌注(OGD-Rep)诱导的细胞死亡的保护作用被抗氧化反应元件(ARE)诱饵寡核苷酸显着减弱,这表明THSWD的保护作用可能至少部分受Nrf2介导的相调节。 II酶。因此,我们的数据将有助于阐明THSWD的神经保护作用的分子机制。

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