| Literature DB >> 29514072 |
Sarah J Mitchell1, Michel Bernier1, Miguel A Aon2, Sonia Cortassa3, Eun Young Kim4, Evandro F Fang5, Hector H Palacios1, Ahmed Ali1, Ignacio Navas-Enamorado1, Andrea Di Francesco1, Tamzin A Kaiser1, Tyler B Waltz5, Ning Zhang6, James L Ellis7, Peter J Elliott7, David W Frederick8, Vilhelm A Bohr5, Mark S Schmidt9, Charles Brenner9, David A Sinclair10, Anthony A Sauve6, Joseph A Baur8, Rafael de Cabo11.
Abstract
The role in longevity and healthspan of nicotinamide (NAM), the physiological precursor of NAD+, is elusive. Here, we report that chronic NAM supplementation improves healthspan measures in mice without extending lifespan. Untargeted metabolite profiling of the liver and metabolic flux analysis of liver-derived cells revealed NAM-mediated improvement in glucose homeostasis in mice on a high-fat diet (HFD) that was associated with reduced hepatic steatosis and inflammation concomitant with increased glycogen deposition and flux through the pentose phosphate and glycolytic pathways. Targeted NAD metabolome analysis in liver revealed depressed expression of NAM salvage in NAM-treated mice, an effect counteracted by higher expression of de novo NAD biosynthetic enzymes. Although neither hepatic NAD+ nor NADP+ was boosted by NAM, acetylation of some SIRT1 targets was enhanced by NAM supplementation in a diet- and NAM dose-dependent manner. Collectively, our results show health improvement in NAM-supplemented HFD-fed mice in the absence of survival effects. Published by Elsevier Inc.Entities:
Keywords: NAD; NAMPT; aging; calorie restriction mimetics; dietary interventions; geroscience; high-fat diet; nicotinamide; sirtuin
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Year: 2018 PMID: 29514072 PMCID: PMC5854409 DOI: 10.1016/j.cmet.2018.02.001
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287