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Nicotinamide Phosphoribosyltransferase as a Key Molecule of the Aging/Senescence Process.

Fiqri D KhaidizarYasumasa BesshoYasukazu Nakahata
Published in: International journal of molecular sciences (2021)
Aging is a phenomenon underlined by complex molecular and biochemical changes that occur over time. One of the metabolites that is gaining strong research interest is nicotinamide adenine dinucleotide, NAD+, whose cellular level has been shown to decrease with age in various tissues of model animals and humans. Administration of NAD+ precursors, nicotinamide mononucleotide (NMN) and nicotinamide riboside (NR), to supplement NAD+ production through the NAD+ salvage pathway has been demonstrated to slow down aging processes in mice. Therefore, NAD+ is a critical metabolite now understood to mitigate age-related tissue function decline and prevent age-related diseases in aging animals. In human clinical trials, administration of NAD+ precursors to the elderly is being used to address systemic age-associated physiological decline. Among NAD+ biosynthesis pathways in mammals, the NAD+ salvage pathway is the dominant pathway in most of tissues, and NAMPT is the rate limiting enzyme of this pathway. However, only a few activators of NAMPT, which are supposed to increase NAD+, have been developed so far. In this review, we will focus on the importance of NAD+ and the possible application of an activator of NAMPT to promote successive aging.
Keyphrases
  • clinical trial
  • endothelial cells
  • gene expression
  • randomized controlled trial
  • metabolic syndrome
  • adipose tissue
  • skeletal muscle
  • induced pluripotent stem cells
  • phase iii
  • nuclear factor