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- W1519210048 abstract "The precise mechanisms of antioxidant-mediated longevity are poorly understood. We show that an antioxidant treatment can extend the lifespan of Caenorhabditis elegans (C. elegans) through the nuclear translocation of the forkhead box O transcription factor (FoxO) homolog DAF-16. This pathway was found to involve 3-phosphoinositide-dependent kinase-1 (PDK-1) and serum- and glucocorticoid-regulated kinase-1 (SGK-1), distinct from the known oxidative stress-mediated mechanism in which FoxO3a translocation is regulated by c-Jun N-terminal kinase (JNK) and mammalian sterile 20-like kinase-1 (MST-1). The differences in the mechanisms of FoxO activation by antioxidants and oxidants result in differences in FoxO phosphorylation and target gene expression. Based on these results, we found that a combination of early antioxidant treatment and late oxidant treatment is most effective for lifespan extension in C. elegans. © 2013 BioFactors, 40(2):247–257, 2014" @default.
- W1519210048 created "2016-06-24" @default.
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- W1519210048 creator A5072667589 @default.
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- W1519210048 date "2013-09-30" @default.
- W1519210048 modified "2023-10-18" @default.
- W1519210048 title "A DAF-16/FoxO3a-dependent longevity signal is initiated by antioxidants" @default.
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- W1519210048 doi "https://doi.org/10.1002/biof.1146" @default.
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