4.8 Article

The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice

Journal

NATURE METABOLISM
Volume 3, Issue 12, Pages 1706-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s42255-021-00491-8

Keywords

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Funding

  1. National Key Research and Development Program of China [2016YFA0100602, 2017YFA0103302]
  2. National Natural Science Foundation of China [81472709, 31671425, 31871380, 82130045, 92049304, 91749203, 82030039, 81370730, 81571512]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB39010500]
  4. Key Laboratory of Tissue Microenvironment and Tumor of the Chinese Academy of Sciences [201506, 201706, 202008]
  5. Anti-Ageing Collaborative Program of SIBS and By-Health [C01201911260006]
  6. University and Locality Collaborative Development Program of Yantai [2019XDRHXMRC08, 2020XDRHXMXK02, 2021XDHZ082]
  7. US DoD PCRP [PC111703]
  8. US NIH [R37 -AG013925, P01 AG062413]
  9. Connor Fund
  10. Noaber Foundation
  11. Yantai Double Hundred Program

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The study demonstrates that procyanidin C1, a natural compound found in grape seeds, has the potential to extend the healthspan and lifespan of mice by acting on senescent cells, showing specific effects on senescent cells and potential as a clinical intervention to delay age-related pathologies.
Ageing-associated functional decline of organs and increased risk for age-related chronic pathologies is driven in part by the accumulation of senescent cells, which develop the senescence-associated secretory phenotype (SASP). Here we show that procyanidin C1 (PCC1), a polyphenolic component of grape seed extract (GSE), increases the healthspan and lifespan of mice through its action on senescent cells. By screening a library of natural products, we find that GSE, and PCC1 as one of its active components, have specific effects on senescent cells. At low concentrations, PCC1 appears to inhibit SASP formation, whereas it selectively kills senescent cells at higher concentrations, possibly by promoting production of reactive oxygen species and mitochondrial dysfunction. In rodent models, PCC1 depletes senescent cells in a treatment-damaged tumour microenvironment and enhances therapeutic efficacy when co-administered with chemotherapy. Intermittent administration of PCC1 to either irradiated, senescent cell-implanted or naturally aged old mice alleviates physical dysfunction and prolongs survival. We identify PCC1 as a natural senotherapeutic agent with in vivo activity and high potential for further development as a clinical intervention to delay, alleviate or prevent age-related pathologies. The polyphenol procyanidin C1, a compound found in grape seeds, possesses senomorphic or senolytic activity and is shown to extend the healthspan and survival of old mice and in various models of senescence-associated disability.

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