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Metabolic shift from glycogen to trehalose promotes lifespan and healthspan in Caenorhabditis elegans
Yonghak Seo, Samuel F. Kingsley, Griffin H. Walker, Michelle A. Mondoux, Heidi A. Tissenbaum
Proceedings of the National Academy of Sciences · 2018 · ▲ 98 citations
Abstract
, a key enzyme in glycogen synthesis, can extend lifespan, prolong healthspan(definition), and limit the detrimental effects of a high-sugar diet. Importantly, limiting glycogen storage leads to a metabolic shift whereby glucose is now stored as trehalose. Two additional means to increase trehalose show similar longevity extension. Increased trehalose is entirely dependent on a functional FOXO transcription factor DAF-16 and autophagy(definition) to promote lifespan and healthspan extension. Our results reveal that when glucose is stored as glycogen, it is detrimental, whereas, when stored as trehalose, animals live a longer, healthier life if DAF-16 is functional. Taken together, these results demonstrate that trehalose modulation may be an avenue for combatting high-sugar-diet pathology.
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- 10.1073/pnas.1714178115
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- 2026-09-02 MST
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APA
Seo, Y., Kingsley, S.F., Walker, G.H., Mondoux, M.A., & Tissenbaum, H.A. (2018). Metabolic shift from glycogen to trehalose promotes lifespan and healthspan in Caenorhabditis elegans. <em>Proceedings of the National Academy of Sciences</em>. https://doi.org/10.1073/pnas.1714178115
Vancouver
Seo Y, Kingsley SF, Walker GH, Mondoux MA, Tissenbaum HA. Metabolic shift from glycogen to trehalose promotes lifespan and healthspan in Caenorhabditis elegans. Proceedings of the National Academy of Sciences. 2018. doi:10.1073/pnas.1714178115.
BibTeX
@article{yonghak2018Metabo,
title = {Metabolic shift from glycogen to trehalose promotes lifespan and healthspan in Caenorhabditis elegans},
author = {Yonghak Seo and Samuel F. Kingsley and Griffin H. Walker and Michelle A. Mondoux and Heidi A. Tissenbaum},
journal = {Proceedings of the National Academy of Sciences},
year = {2018},
doi = {10.1073/pnas.1714178115},
}
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