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叔丁基对苯二酚激活NF-E2相关因子2并诱导血红素加氧酶-1,从而保护PC12细胞免受溴氰菊酯介导的氧化应激。

NF-E2 related factor 2 activation and heme oxygenase-1 induction by tert-butylhydroquinone protect against deltamethrin-mediated oxidative stress in PC12 cells.

作者信息

Li Huang Yuan, Zhong Yu Fang, Wu Si Ying, Shi Nian

机构信息

Department of Occupational and Environmental Health, Major Subject of Environment and Health of Fujian Key Universities, School of Public Health, Fujian Medical University, Fuzhou 350004 China.

出版信息

Chem Res Toxicol. 2007 Sep;20(9):1242-51. doi: 10.1021/tx700076q. Epub 2007 Aug 4.

Abstract

Recent findings suggest that oxidative stress caused by pyrethroid pesticides could be closely involved in the neurotoxicity. tert-Butylhydroquinone ( tBHQ) is a known inducer of Nrf2-mediated transcription, and treatment of cells with tBHQ can confer protection against H 2O 2 and 6-hydroxydopamine (6-OHDA). In this study, we investigated the neuroprotective effect of tBHQ against deltamethrin (DM)-induced oxidative stress using rat PC12 adrenal pheochromocytoma cells. The pretreatment of PC12 cells with tBHQ significantly reduced DM-induced generation of reactive oxygen species (ROS) and increased intracellular ionized calcium ([Ca (2+)] i). We also observed that DM or tBHQ induced the expression of NF-E2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1), a Nrf2-regulated gene. In addition, the Nrf2 antioxidant responsive element (ARE) pathways activated by tBHQ caused a partial inhibition of the DM-induced Nrf2 and HO-1 expression. Altogether, our data clearly indicate that an activation of Nrf2/ARE pathways in PC12 cells by tBHQ treatment protects cells from DM-induced oxidative stress and regulates DM- mediated adaptive responses in PC12 cells via translocation of Nrf2.

摘要

最近的研究结果表明,拟除虫菊酯类农药引起的氧化应激可能与神经毒性密切相关。叔丁基对苯二酚(tBHQ)是一种已知的Nrf2介导转录的诱导剂,用tBHQ处理细胞可使其免受H2O2和6-羟基多巴胺(6-OHDA)的损伤。在本研究中,我们使用大鼠PC12肾上腺嗜铬细胞瘤细胞研究了tBHQ对溴氰菊酯(DM)诱导的氧化应激的神经保护作用。用tBHQ预处理PC12细胞可显著降低DM诱导的活性氧(ROS)生成,并增加细胞内离子钙([Ca(2+)]i)。我们还观察到,DM或tBHQ可诱导NF-E2相关因子2(Nrf2)和血红素加氧酶-1(HO-1,一种Nrf2调控的基因)的表达。此外,tBHQ激活的Nrf2抗氧化反应元件(ARE)途径可部分抑制DM诱导的Nrf2和HO-1表达。总之,我们的数据清楚地表明,tBHQ处理激活PC12细胞中的Nrf2/ARE途径可保护细胞免受DM诱导的氧化应激,并通过Nrf2的易位调节PC12细胞中DM介导的适应性反应。

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