IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v10y2019i1d10.1038_s41467-019-11078-z.html
   My bibliography  Save this article

Boosting NAD+ with a small molecule that activates NAMPT

Author

Listed:
  • Stephen J. Gardell

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona
    AdventHealth-Orlando)

  • Meghan Hopf

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona
    AdventHealth-Orlando)

  • Asima Khan

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona
    AdventHealth-Orlando)

  • Mauro Dispagna

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona)

  • E. Hampton Sessions

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona)

  • Rebecca Falter

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona)

  • Nidhi Kapoor

    (AdventHealth-Orlando
    Sanford Burnham Prebys Medical Discovery Institute at Lake Nona)

  • Jeanne Brooks

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona)

  • Jeffrey Culver

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona)

  • Chris Petucci

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona)

  • Chen-Ting Ma

    (Sanford Burnham Prebys Medical Discovery Institute)

  • Steven E. Cohen

    (Global Business Development)

  • Jun Tanaka

    (Ltd, Shinagawa Research & Development Center)

  • Emmanuel S. Burgos

    (Albert Einstein College of Medicine)

  • Jennifer S. Hirschi

    (Binghamton University)

  • Steven R. Smith

    (Sanford Burnham Prebys Medical Discovery Institute at Lake Nona
    AdventHealth-Orlando)

  • Eduard Sergienko

    (Sanford Burnham Prebys Medical Discovery Institute)

  • Anthony B. Pinkerton

    (Sanford Burnham Prebys Medical Discovery Institute)

Abstract

Pharmacological strategies that boost intracellular NAD+ are highly coveted for their therapeutic potential. One approach is activation of nicotinamide phosphoribosyltransferase (NAMPT) to increase production of nicotinamide mononucleotide (NMN), the predominant NAD+ precursor in mammalian cells. A high-throughput screen for NAMPT activators and hit-to-lead campaign yielded SBI-797812, a compound that is structurally similar to active-site directed NAMPT inhibitors and blocks binding of these inhibitors to NAMPT. SBI-797812 shifts the NAMPT reaction equilibrium towards NMN formation, increases NAMPT affinity for ATP, stabilizes phosphorylated NAMPT at His247, promotes consumption of the pyrophosphate by-product, and blunts feedback inhibition by NAD+. These effects of SBI-797812 turn NAMPT into a “super catalyst” that more efficiently generates NMN. Treatment of cultured cells with SBI-797812 increases intracellular NMN and NAD+. Dosing of mice with SBI-797812 elevates liver NAD+. Small molecule NAMPT activators such as SBI-797812 are a pioneering approach to raise intracellular NAD+ and realize its associated salutary effects.

Suggested Citation

  • Stephen J. Gardell & Meghan Hopf & Asima Khan & Mauro Dispagna & E. Hampton Sessions & Rebecca Falter & Nidhi Kapoor & Jeanne Brooks & Jeffrey Culver & Chris Petucci & Chen-Ting Ma & Steven E. Cohen &, 2019. "Boosting NAD+ with a small molecule that activates NAMPT," Nature Communications, Nature, vol. 10(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11078-z
    DOI: 10.1038/s41467-019-11078-z
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-019-11078-z
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-019-11078-z?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Björn Klabunde & André Wesener & Wilhelm Bertrams & Isabell Beinborn & Nicole Paczia & Kristin Surmann & Sascha Blankenburg & Jochen Wilhelm & Javier Serrania & Kèvin Knoops & Eslam M. Elsayed & Katri, 2023. "NAD+ metabolism is a key modulator of bacterial respiratory epithelial infections," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    2. Liang Yang & Junfeng Shen & Chunhua Liu & Zhonghua Kuang & Yong Tang & Zhengjiang Qian & Min Guan & Yongfeng Yang & Yang Zhan & Nan Li & Xiang Li, 2023. "Nicotine rebalances NAD+ homeostasis and improves aging-related symptoms in male mice by enhancing NAMPT activity," Nature Communications, Nature, vol. 14(1), pages 1-17, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11078-z. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.