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Fisetin: hormesis accounts for many of its chemoprotective effects
Edward J Calabrese1, Peter Pressman2, A Wallace Hayes3
1Department of Environmental Health, School of Public Health and Health Sciences, University of Massachusetts, Morrill I-N344, Amherst, MA, 01003, USA. edwardc@umass.edu.
Abstract:
The present paper provides the first integrated assessment of the capacity of the flavonol, fisetin, to induce hormetic dose responses. Fisetin was shown to induce hormetic dose responses in cellular and in vivo animal model systems affecting a broad range of endpoints of potential therapeutic and public health significance across the entire lifespan. Fisetin was effective in slowing aging processes, acting as a senolytic agent in multiple organ systems, in an hormetic fashion. In addition, fisetin was broadly neuroprotective, including during fetal development, and preventing the toxicity of methylmercury. Since these findings indicate that fisetin may have the potential to induce multi-system chemoprotective effects, it indicates the need to better clarify the absorption and bioavailability of fisetin and ways to enhance its efficiency.
Insights
The flavonol fisetin shows potential for health benefits by inducing hormetic dose responses, slowing aging, and protecting the nervous system. Further research is needed to optimize its absorption and bioavailability.
Area of Science:
- Biogerontology
- Pharmacology
- Toxicology
Background:
- Hormesis, a dose-response phenomenon, is increasingly recognized for its health implications.
- Flavonoids, like fisetin, are plant compounds with potential therapeutic properties.
- Understanding fisetin's hormetic capacity is crucial for its application in health and disease.
Purpose of the Study:
- To assess the capacity of fisetin to induce hormetic dose responses.
- To evaluate fisetin's effects on aging processes and neuroprotection.
- To identify potential therapeutic applications of fisetin.
Main Methods:
- Integrated assessment of fisetin's dose-response effects.
- Evaluation in cellular and in vivo animal models.
- Analysis of effects on aging, senolysis, and neuroprotection endpoints.
Main Results:
- Fisetin demonstrated hormetic dose responses across various endpoints.
- It effectively slowed aging processes and acted as a senolytic agent.
- Fisetin provided broad neuroprotection, including against methylmercury toxicity.
Conclusions:
- Fisetin exhibits multi-system chemoprotective potential through hormesis.
- Its senolytic and neuroprotective effects warrant further investigation.
- Optimizing fisetin's absorption and bioavailability is essential for therapeutic enhancement.
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