Targeting senescence induced by age or chemotherapy with a polyphenol-rich natural extract improves longevity and healthspan in mice
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Published:2024-07-01
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ISSN:2662-8465
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Container-title:Nature Aging
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language:en
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Short-container-title:Nat Aging
Author:
Zumerle SaraORCID, Sarill MilesORCID, Saponaro Miriam, Colucci ManuelORCID, Contu Liliana, Lazzarini Edoardo, Sartori Roberta, Pezzini Camilla, Rinaldi Anna, Scanu Anna, Sgrignani Jacopo, Locatelli Patrizia, Sabbadin Marianna, Valdata Aurora, Brina Daniela, Giacomini IsabellaORCID, Rizzo BeatriceORCID, Pierantoni Alessandra, Sharifi Saman, Bressan Silvia, Altomare Claudia, Goshovska Yulia, Giraudo Chiara, Luisetto Roberto, Iaccarino Luca, Torcasio Cristina, Mosole Simone, Pasquini Emiliano, Rinaldi Andrea, Pellegrini LauraORCID, Peron GregorioORCID, Fassan MatteoORCID, Masiero Stefano, Giori Andrea Maria, Dall’Acqua Stefano, Auwerx Johan, Cippà Pietro, Cavalli Andrea, Bolis MarcoORCID, Sandri MarcoORCID, Barile LucioORCID, Montopoli MonicaORCID, Alimonti AndreaORCID
Abstract
AbstractAccumulating senescent cells within tissues contribute to the progression of aging and age-related diseases. Botanical extracts, rich in phytoconstituents, present a useful resource for discovering therapies that could target senescence and thus improve healthspan. Here, we show that daily oral administration of a standardized extract of Salvia haenkei (Haenkenium (HK)) extended lifespan and healthspan of naturally aged mice. HK treatment inhibited age-induced inflammation, fibrosis and senescence markers across several tissues, as well as increased muscle strength and fur thickness compared with age-matched controls. We also found that HK treatment reduced acutely induced senescence by the chemotherapeutic agent doxorubicin, using p16LUC reporter mice. We profiled the constituent components of HK by mass spectrometry, and identified luteolin—the most concentrated flavonoid in HK—as a senomorphic compound. Mechanistically, by performing surface plasmon resonance and in situ proximity ligation assay, we found that luteolin disrupted the p16–CDK6 interaction. This work demonstrates that administration of HK promotes longevity in mice, possibly by modulating cellular senescence and by disrupting the p16–CDK6 interaction.
Publisher
Springer Science and Business Media LLC
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