Targeting NAD+ in Metabolic Disease: New Insights Into an Old Molecule

Andrew A Philp, Gareth G Lavery, Yasir Elhassan

Research output: Contribution to journalReview articlepeer-review

43 Citations (Scopus)

Abstract

Nicotinamide adenine dinucleotide (NAD+) is an established cofactor for enzymes serving cellular metabolic reactions. More recent research identified NAD+ as a signaling molecule and substrate for sirtuins and poly-adenosine 5'-diphosphate polymerases; enzymes that regulate protein deacetylation and DNA repair, and translate changes in energy status into metabolic adaptations. Deranged NAD+ homeostasis and concurrent alterations in mitochondrial function are intrinsic in metabolic disorders, such as type 2 diabetes, nonalcoholic fatty liver, and age-related diseases. Contemporary NAD+ precursors show promise as nutraceuticals to restore target tissue NAD+ and have demonstrated the ability to improve mitochondrial function and sirtuin-dependent signaling. This review discusses the accumulating evidence for targeting NAD+ metabolism in metabolic disease, maps the different strategies for NAD+ boosting, and addresses the challenges and open questions in the field. The health potential of targeting NAD+ homeostasis will inform clinical study design to identify nutraceutical approaches for combating metabolic disease and the unwanted effects of aging.

Original languageEnglish
Pages (from-to)816-835
Number of pages20
JournalEndocrine pathology
Volume1
Issue number7
DOIs
Publication statusPublished - 15 May 2017

Keywords

  • nicotinamide riboside
  • nicotinamide mononucleotide
  • mitochondria
  • diabetes
  • nonalcoholic fatty liver disease
  • aging

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