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A triple drug combination targeting components of the nutrient-sensing network maximizes longevity.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2019 Oct 15; Vol. 116 (42), pp. 20817-20819. Date of Electronic Publication: 2019 Sep 30. - Publication Year :
- 2019
-
Abstract
- Increasing life expectancy is causing the prevalence of age-related diseases to rise, and there is an urgent need for new strategies to improve health at older ages. Reduced activity of insulin/insulin-like growth factor signaling (IIS) and mechanistic target of rapamycin (mTOR) nutrient-sensing signaling network can extend lifespan and improve health during aging in diverse organisms. However, the extensive feedback in this network and adverse side effects of inhibition imply that simultaneous targeting of specific effectors in the network may most effectively combat the effects of aging. We show that the mitogen-activated protein kinase kinase (MEK) inhibitor trametinib, the mTOR complex 1 (mTORC1) inhibitor rapamycin, and the glycogen synthase kinase-3 (GSK-3) inhibitor lithium act additively to increase longevity in Drosophila Remarkably, the triple drug combination increased lifespan by 48%. Furthermore, the combination of lithium with rapamycin cancelled the latter's effects on lipid metabolism. In conclusion, a polypharmacology approach of combining established, prolongevity drug inhibitors of specific nodes may be the most effective way to target the nutrient-sensing network to improve late-life health.<br />Competing Interests: The authors declare no competing interest.<br /> (Copyright © 2019 the Author(s). Published by PNAS.)
- Subjects :
- Aged
Aging metabolism
Animals
Drosophila genetics
Drosophila growth & development
Drosophila metabolism
Drosophila Proteins genetics
Drosophila Proteins metabolism
Drug Combinations
Female
Glycogen Synthase Kinase 3 antagonists & inhibitors
Glycogen Synthase Kinase 3 genetics
Glycogen Synthase Kinase 3 metabolism
Humans
Mechanistic Target of Rapamycin Complex 1 antagonists & inhibitors
Mechanistic Target of Rapamycin Complex 1 genetics
Mechanistic Target of Rapamycin Complex 1 metabolism
Middle Aged
Signal Transduction drug effects
Aging drug effects
Drosophila drug effects
Lithium pharmacology
Longevity drug effects
Nutrients metabolism
Pyridones pharmacology
Pyrimidinones pharmacology
Sirolimus pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 116
- Issue :
- 42
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 31570569
- Full Text :
- https://doi.org/10.1073/pnas.1913212116