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A triple drug combination targeting components of the nutrient-sensing network maximizes longevity.

Citation
Castillo-Quan, J. I., et al. “A Triple Drug Combination Targeting Components Of The Nutrient-Sensing Network Maximizes Longevity.”. Proceedings Of The National Academy Of Sciences Of The United States Of America, pp. 20817-20819.
Center Joslin Diabetes Center
Author Jorge Iván Castillo-Quan, Luke S Tain, Kerri J Kinghorn, Li Li, Sebastian Grönke, Yvonne Hinze, Keith Blackwell, Ivana Bjedov, Linda Partridge
Keywords aging, lithium, polypharmacology, Rapamycin, trametinib
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 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.

Year of Publication
2019
Journal
Proceedings of the National Academy of Sciences of the United States of America
Volume
116
Issue
42
Number of Pages
20817-20819
Date Published
12/2019
ISSN Number
1091-6490
DOI
10.1073/pnas.1913212116
Alternate Journal
Proc. Natl. Acad. Sci. U.S.A.
PMID
31570569
PMCID
PMC6800352
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