Literature DB >> 22503440

NADPH oxidases: novel therapeutic targets for neurodegenerative diseases.

Hui-Ming Gao1, Hui Zhou, Jau-Shyong Hong.   

Abstract

Oxidative stress is a key pathologic factor in neurodegenerative diseases such as Alzheimer and Parkinson diseases (AD, PD). The failure of free-radical-scavenging antioxidants in clinical trials pinpoints an urgent need to identify and to block major sources of oxidative stress in neurodegenerative diseases. As a major superoxide-producing enzyme complex in activated phagocytes, phagocyte NADPH oxidase (PHOX) is essential for host defense. However, recent preclinical evidence has underscored a pivotal role of overactivated PHOX in chronic neuroinflammation and progressive neurodegeneration. Deficiency in PHOX subunits mitigates neuronal damage induced by diverse insults/stresses relevant to neurodegenerative diseases. More importantly, suppression of PHOX activity correlates with reduced neuronal impairment in models of neurodegenerative diseases. The discovery of PHOX and non-phagocyte NADPH oxidases in astroglia and neurons further reinforces the crucial role of NADPH oxidases in oxidative stress-mediated chronic neurodegeneration. Thus, proper modulation of NADPH oxidase activity might hold therapeutic potential for currently incurable neurodegenerative diseases. Published by Elsevier Ltd.

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Year:  2012        PMID: 22503440      PMCID: PMC3477578          DOI: 10.1016/j.tips.2012.03.008

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  107 in total

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7.  Inhibiting the Activity of NADPH Oxidase in Cancer.

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8.  NOX2 drives M1-like microglial/macrophage activation and neurodegeneration following experimental traumatic brain injury.

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9.  Diazoxide pretreatment prevents Aβ1-42 induced oxidative stress in cholinergic neurons via alleviating NOX2 expression.

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Review 10.  Imine reductases: a comparison of glutamate dehydrogenase to ketimine reductases in the brain.

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