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Benefits of Fisetin

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Evidence-Based Benefits

  • Senolytic activity — Yousefzadeh et al. (2018) screened 10 flavonoids and identified fisetin as the most potent natural senolytic, selectively killing senescent cells while sparing healthy cells in both human and mouse tissues
  • Lifespan extension — in the same study, fisetin administered to 85-week-old mice (equivalent to ~75 human years) extended median remaining lifespan by approximately 10% and reduced senescence biomarkers in multiple tissues
  • Anti-inflammatory — fisetin reduces SASP factors (IL-6, IL-8, MCP-1, TNF-α) secreted by senescent cells, which drive age-related chronic inflammation and tissue dysfunction
  • Neuroprotection — preclinical studies show fisetin maintains cognitive function in Alzheimer's models by reducing neuroinflammation, oxidative stress, and amyloid-beta pathology (Currais et al., 2014)
  • Antioxidant — fisetin directly scavenges reactive oxygen species and upregulates endogenous antioxidant enzymes including glutathione, catalase, and superoxide dismutase

What the Research Says

Fisetin's senolytic properties were established by Yousefzadeh et al. (2018) at the Mayo Clinic, who showed it was the most effective of 10 flavonoids tested at clearing senescent cells both in vitro and in vivo. The late-life lifespan extension in mice was particularly striking because it demonstrated benefit even when treatment began at advanced age. Currais et al. (2014) showed neuroprotective effects in Alzheimer's mouse models. The Mayo Clinic AFFIRM trial is testing fisetin in elderly women with frailty markers. Kirkland and colleagues have pioneered the senolytic field and consider fisetin among the most promising candidates alongside dasatinib+quercetin. The main limitation is poor oral bioavailability due to low water solubility, which liposomal formulations may address.

References

  1. (). Fisetin is a senotherapeutic that extends health and lifespan. EBioMedicine. DOI
  2. (). Modulation of p25 and inflammatory pathways by fisetin maintains cognitive function in Alzheimer's disease transgenic mice. Aging Cell. DOI
  3. (). New agents that target senescent cells: the flavone, fisetin, and the BCL-XL inhibitors, A1331852 and A1155463. Aging. DOI