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

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 gra...

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Autores principales: Xu, Qixia, Fu, Qiang, Li, Zi, Liu, Hanxin, Wang, Ying, Lin, Xu, He, Ruikun, Zhang, Xuguang, Ju, Zhenyu, Campisi, Judith, Kirkland, James L., Sun, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688144/
https://www.ncbi.nlm.nih.gov/pubmed/34873338
http://dx.doi.org/10.1038/s42255-021-00491-8
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author Xu, Qixia
Fu, Qiang
Li, Zi
Liu, Hanxin
Wang, Ying
Lin, Xu
He, Ruikun
Zhang, Xuguang
Ju, Zhenyu
Campisi, Judith
Kirkland, James L.
Sun, Yu
author_facet Xu, Qixia
Fu, Qiang
Li, Zi
Liu, Hanxin
Wang, Ying
Lin, Xu
He, Ruikun
Zhang, Xuguang
Ju, Zhenyu
Campisi, Judith
Kirkland, James L.
Sun, Yu
author_sort Xu, Qixia
collection PubMed
description 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.
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spelling pubmed-86881442022-01-05 The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice Xu, Qixia Fu, Qiang Li, Zi Liu, Hanxin Wang, Ying Lin, Xu He, Ruikun Zhang, Xuguang Ju, Zhenyu Campisi, Judith Kirkland, James L. Sun, Yu Nat Metab Article 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. Nature Publishing Group UK 2021-12-06 2021 /pmc/articles/PMC8688144/ /pubmed/34873338 http://dx.doi.org/10.1038/s42255-021-00491-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Xu, Qixia
Fu, Qiang
Li, Zi
Liu, Hanxin
Wang, Ying
Lin, Xu
He, Ruikun
Zhang, Xuguang
Ju, Zhenyu
Campisi, Judith
Kirkland, James L.
Sun, Yu
The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice
title The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice
title_full The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice
title_fullStr The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice
title_full_unstemmed The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice
title_short The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice
title_sort flavonoid procyanidin c1 has senotherapeutic activity and increases lifespan in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688144/
https://www.ncbi.nlm.nih.gov/pubmed/34873338
http://dx.doi.org/10.1038/s42255-021-00491-8
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