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Dietary thiols accelerate aging of C. elegans.
- Source :
-
Nature communications [Nat Commun] 2021 Jul 15; Vol. 12 (1), pp. 4336. Date of Electronic Publication: 2021 Jul 15. - Publication Year :
- 2021
-
Abstract
- Glutathione (GSH) is the most abundant cellular antioxidant. As reactive oxygen species (ROS) are widely believed to promote aging and age-related diseases, and antioxidants can neutralize ROS, it follows that GSH and its precursor, N-acetyl cysteine (NAC), are among the most popular dietary supplements. However, the long- term effects of GSH or NAC on healthy animals have not been thoroughly investigated. We employed C. elegans to demonstrate that chronic administration of GSH or NAC to young or aged animals perturbs global gene expression, inhibits skn-1-mediated transcription, and accelerates aging. In contrast, limiting the consumption of dietary thiols, including those naturally derived from the microbiota, extended lifespan. Pharmacological GSH restriction activates the unfolded protein response and increases proteotoxic stress resistance in worms and human cells. It is thus advantageous for healthy individuals to avoid excessive dietary antioxidants and, instead, rely on intrinsic GSH biosynthesis, which is fine-tuned to match the cellular redox status and to promote homeostatic ROS signaling.<br /> (© 2021. The Author(s).)
- Subjects :
- Aging genetics
Aging physiology
Animals
Animals, Genetically Modified
Caenorhabditis elegans Proteins genetics
DNA-Binding Proteins genetics
Dietary Supplements
Escherichia coli
Female
Fibroblasts metabolism
Gene Expression Regulation drug effects
Glutathione metabolism
Humans
Male
Paraquat pharmacology
Reactive Oxygen Species metabolism
Sulfhydryl Compounds metabolism
Transcription Factors genetics
Unfolded Protein Response physiology
Acetylcysteine pharmacology
Aging drug effects
Caenorhabditis elegans drug effects
Caenorhabditis elegans physiology
Glutathione pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 34267196
- Full Text :
- https://doi.org/10.1038/s41467-021-24634-3