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Review
. 2017 Mar;54(2):1440-1455.
doi: 10.1007/s12035-016-9707-7. Epub 2016 Feb 5.

Nrf2 Weaves an Elaborate Network of Neuroprotection Against Stroke

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Review

Nrf2 Weaves an Elaborate Network of Neuroprotection Against Stroke

Shuai Jiang et al. Mol Neurobiol. 2017 Mar.

Abstract

Nuclear factor erythroid 2-related factor 2 (Nrf2) is a neuroprotective transcription factor that has recently attracted increased attention. Stroke, a common and serious neurological disease, is currently a leading cause of death in the USA so far. It is therefore of vital importance to explore how Nrf2 behaves in stroke. In this review, we first introduce the structural features of Nrf2 and Kelch-like ECH-associated protein 1 (Keap1) and briefly depict the activation, inactivation, and regulation processes of the Nrf2 pathway. Next, we discuss the physiopathological mechanisms, upstream modulators, and downstream targets of the Nrf2 pathway. Following this background, we expand our discussion to the roles of Nrf2 in ischemic and hemorrhagic stroke and provide several potential future directions. The information presented here may be useful in the design of future experimental research and increase the likelihood of using Nrf2 as a therapeutic target for stroke in the future.

Keywords: Hemorrhage; Ischemia; Nuclear factor erythroid 2-related factor 2; Oxidative stress.

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References

    1. Biochemistry. 2003 Apr 15;42(14):4300-9 - PubMed
    1. J Pathol. 2014 Dec;234(4):538-47 - PubMed
    1. Int J Dev Neurosci. 2014 Nov;38:79-86 - PubMed
    1. Mol Cell Biol. 2010 Jul;30(13):3275-85 - PubMed
    1. Biochem J. 2011 Dec 1;440(2):167-74 - PubMed

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