IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-36543-8.html
   My bibliography  Save this article

Nicotine rebalances NAD+ homeostasis and improves aging-related symptoms in male mice by enhancing NAMPT activity

Author

Listed:
  • Liang Yang

    (Chinese Academy of Sciences
    Brain Cognition and Brain Disease Institute (BCBDI)
    Guangdong Provincial Key Laboratory of Brain Connectome, Shenzhen Key Laboratory of Viral Vectors for Biomedicine)

  • Junfeng Shen

    (Chinese Academy of Sciences
    Shenzhen Institute of Synthetic Biology)

  • Chunhua Liu

    (Chinese Academy of Sciences
    Brain Cognition and Brain Disease Institute (BCBDI)
    Guangdong Provincial Key Laboratory of Brain Connectome, Shenzhen Key Laboratory of Viral Vectors for Biomedicine)

  • Zhonghua Kuang

    (Chinese Academy of Sciences
    Institute of Biomedical and Health Engineering
    Paul C. Lauterbur Research Center for Biomedical Imaging)

  • Yong Tang

    (Chinese Academy of Sciences
    Brain Cognition and Brain Disease Institute (BCBDI))

  • Zhengjiang Qian

    (Chinese Academy of Sciences
    Brain Cognition and Brain Disease Institute (BCBDI))

  • Min Guan

    (Chinese Academy of Sciences
    Institute of Biomedicine and Biotechnology)

  • Yongfeng Yang

    (Chinese Academy of Sciences
    Institute of Biomedical and Health Engineering
    Paul C. Lauterbur Research Center for Biomedical Imaging)

  • Yang Zhan

    (Chinese Academy of Sciences
    Brain Cognition and Brain Disease Institute (BCBDI))

  • Nan Li

    (Chinese Academy of Sciences
    Shenzhen Institute of Synthetic Biology
    Chinese Academy of Sciences (CAS) Key Laboratory for Quantitative Engineering Biology)

  • Xiang Li

    (Chinese Academy of Sciences
    Guangdong Provincial Key Laboratory of Brain Connectome, Shenzhen Key Laboratory of Viral Vectors for Biomedicine)

Abstract

Imbalances in NAD+ homeostasis have been linked to aging and various diseases. Nicotine, a metabolite of the NAD+ metabolic pathway, has been found to possess anti-inflammatory and neuroprotective properties, yet the underlying molecular mechanisms remained unknown. Here we find that, independent of nicotinic acetylcholine receptors, low-dose nicotine can restore the age-related decline of NAMPT activity through SIRT1 binding and subsequent deacetylation of NAMPT, thus increasing NAD+ synthesis. 18F-FDG PET imaging revealed that nicotine is also capable of efficiently inhibiting glucose hypermetabolism in aging male mice. Additionally, nicotine ameliorated cellular energy metabolism disorders and deferred age-related deterioration and cognitive decline by stimulating neurogenesis, inhibiting neuroinflammation, and protecting organs from oxidative stress and telomere shortening. Collectively, these findings provide evidence for a mechanism by which low-dose nicotine can activate NAD+ salvage pathways and improve age-related symptoms.

Suggested Citation

  • 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.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36543-8
    DOI: 10.1038/s41467-023-36543-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-36543-8
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-36543-8?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
    ---><---

    References listed on IDEAS

    as
    1. Joseph T. Rodgers & Carlos Lerin & Wilhelm Haas & Steven P. Gygi & Bruce M. Spiegelman & Pere Puigserver, 2005. "Nutrient control of glucose homeostasis through a complex of PGC-1α and SIRT1," Nature, Nature, vol. 434(7029), pages 113-118, March.
    2. Alexander Duncan & Mary P. Heyer & Masago Ishikawa & Stephanie P. B. Caligiuri & Xin-an Liu & Zuxin Chen & Maria Vittoria Micioni Di Bonaventura & Karim S. Elayouby & Jessica L. Ables & William M. How, 2019. "Habenular TCF7L2 links nicotine addiction to diabetes," Nature, Nature, vol. 574(7778), pages 372-377, October.
    3. 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.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    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. Guanlan Hu & Catriona Ling & Lijun Chi & Mehakpreet K. Thind & Samuel Furse & Albert Koulman & Jonathan R. Swann & Dorothy Lee & Marjolein M. Calon & Celine Bourdon & Christian J. Versloot & Barbara M, 2022. "The role of the tryptophan-NAD + pathway in a mouse model of severe malnutrition induced liver dysfunction," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    3. Simeon R. Mihaylov & Lydia M. Castelli & Ya-Hui Lin & Aytac Gül & Nikita Soni & Christopher Hastings & Helen R. Flynn & Oana Păun & Mark J. Dickman & Ambrosius P. Snijders & Robert Goldstone & Oliver, 2023. "The master energy homeostasis regulator PGC-1α exhibits an mRNA nuclear export function," Nature Communications, Nature, vol. 14(1), pages 1-22, December.
    4. Yoona Kim & Peter Clifton, 2018. "Curcumin, Cardiometabolic Health and Dementia," IJERPH, MDPI, vol. 15(10), pages 1-34, September.
    5. Jae Woo Park & Eun Roh & Gil Myoung Kang & So Young Gil & Hyun Kyong Kim & Chan Hee Lee & Won Hee Jang & Se Eun Park & Sang Yun Moon & Seong Jun Kim & So Yeon Jeong & Chae Beom Park & Hyo Sun Lim & Yu, 2023. "Circulating blood eNAMPT drives the circadian rhythms in locomotor activity and energy expenditure," 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:14:y:2023:i:1:d:10.1038_s41467-023-36543-8. 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.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with 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.