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The Nrf2/ARE Pathway as a Potential Therapeutic Target in Neurodegenerative Disease

机译:Nrf2 / ARE途径作为神经退行性疾病的潜在治疗靶点

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摘要

Nuclear factor E2–related factor 2 (Nrf2) is a transcription factor known to induce expression of a variety of cytoprotective and detoxification genes. Several of the genes commonly regulated by Nrf2 have been implicated in protection from neurodegenerative conditions. Work from several laboratories has uncovered the potential for Nrf2-mediated transcription to protect from neurodegeneration resulting from mechanisms involving oxidative stress. For this reason, Nrf2 may be considered a therapeutic target for conditions that are known to involve free radical damage. Because common mechanisms of neurodegeneration, such as mitochondrial dysfunction and build-up of reactive oxygen species, are currently being uncovered, targeting Nrf2 may be valuable in combating conditions with variable causes and etiologies. Most effectively to target this protein in neurodegenerative conditions, a description of the involvement of Nrf2 and potential for neuroprotection must come from laboratory models. Herein, we review the current literature that suggests that Nrf2 may be a valuable therapeutic target for neurodegenerative disease, as well as experiments that illustrate potential mechanisms of protection.
机译:核因子E2相关因子2(Nrf2)是一种转录因子,已知可诱导多种细胞保护和排毒基因的表达。通常由Nrf2调控的几种基因与神经退行性疾病的保护有关。几个实验室的工作发现了Nrf2介导的转录保护免受氧化应激机制引起的神经变性的潜力。因此,对于已知涉及自由基损伤的疾病,Nrf2可被视为治疗靶标。由于目前尚未发现神经变性的常见机制,例如线粒体功能障碍和活性氧的积累,因此靶向Nrf2可能在抵抗病因和病因多变的疾病中具有重要意义。要在神经退行性疾病中最有效地靶向这种蛋白质,对Nrf2参与和神经保护潜力的描述必须来自实验室模型。在本文中,我们回顾了当前的文献,这些文献表明Nrf2可能是神经退行性疾病的有价值的治疗靶标,并通过实验说明了潜在的保护机制。

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  • 来源
    《Antioxidants & Redox Signaling》 |2009年第3期|497-508|共12页
  • 作者单位

    Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin.;

    Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin.|Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.;

    Molecular and Cellular Pharmacology, University of Wisconsin, Madison, Wisconsin.;

    Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.;

    Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.;

    Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.;

    Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.;

    Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.;

    Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.;

    Molecular and Environmental Toxicology Center, University of Wisconsin, Madison, Wisconsin.|Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin.|Molecular and Cellular Pharmacology, University of Wisconsin, Madison, Wisconsin.|Neuroscience Training Program, University of Wisconsin, Madison, Wisconsin.;

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