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基于 Nrf2 介导的 II 相酶的蛋白质组学鉴定对桃红四物汤防治 PC12 细胞氧葡萄糖剥夺损伤的作用。

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.

机构信息

College of Pharmaceutical Sciences, Southwest University, 2 Tiansheng Road, Beibei District, Chongqing 400716, China.

College of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 611137, China.

出版信息

Evid Based Complement Alternat Med. 2014;2014:945814. doi: 10.1155/2014/945814. Epub 2014 May 11.

DOI:10.1155/2014/945814
PMID:24949080
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4037622/
Abstract

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.

摘要

中药方剂桃红四物汤(THSWD)在中国传统上用于治疗脑血管疾病。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。本研究应用基于二维凝胶电泳的蛋白质组学技术,研究了未经 THSWD 处理和经 THSWD 处理的 PC12 细胞之间的不同蛋白质图谱。通过 MALDI-TOF 质谱鉴定出 26 种受 THSWD 影响的蛋白质。GO 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。特别是,其中 6 种被发现是 II 相抗氧化酶,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 6 种 II 相酶的剂量依赖性诱导。此外,还发现 THSWD 的各个成分协同促进 II 相酶的诱导。重要的是,抗氧化反应元件(ARE)诱饵寡核苷酸显著减弱了 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,表明 THSWD 的保护作用可能至少部分受到 Nrf2 介导的 II 相酶的调节。因此,我们的数据将有助于阐明 THSWD 神经保护作用的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/ebbd7e620b22/ECAM2014-945814.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/d3ff77bcc9c3/ECAM2014-945814.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/4413d6173910/ECAM2014-945814.002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/ebbd7e620b22/ECAM2014-945814.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/d3ff77bcc9c3/ECAM2014-945814.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/4413d6173910/ECAM2014-945814.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/e93cf05ac0b5/ECAM2014-945814.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/710c7fabc1db/ECAM2014-945814.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/2ae21da90126/ECAM2014-945814.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141b/4037622/ebbd7e620b22/ECAM2014-945814.006.jpg

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