Exploring the Senotherapeutic Potential of Polyphenols in Aging and Disease: A Literature Review
Luna Braučič Mitrovic1, Khrystyna O Semen1
1University College Venlo, Campus Venlo, Faculty of Science and Engineering, Maastricht University, 5911 BV Venlo, The Netherlands.
Abstract:
Aging is associated with an increased risk of developing many age-related diseases (ARDs), which are of major global health concern. In recent years, cellular senescence, characterized by cell cycle arrest and development of a senescence-associated secretory phenotype (SASP), has emerged as a key mechanism of aging and ARDs and has been increasingly explored as a promising therapeutic target. Among dietary bioactive ingredients, fisetin and quercetin have gained attention because of their potential to act as senolytics and senomorphics. This narrative literature review summarizes existing evidence exploring the potential of fisetin and quercetin to modulate senescence and SASP biomarkers in animal models of aging and progeria, as well as in interventional studies involving human subjects with geriatric syndromes and/or various ARDs. It also provides a brief overview of the molecular mechanisms of senescence and attempts to identify potential drivers and barriers for the clinical translation of those nutrients.
Insights
Dietary compounds fisetin and quercetin show promise in targeting cellular senescence, a key aging mechanism. This review explores their potential to combat age-related diseases (ARDs) by modulating senescence and the senescence-associated secretory phenotype (SASP).
Area of Science:
- Gerontology and cellular biology
- Nutritional science and pharmacology
Background:
- Aging increases the risk of age-related diseases (ARDs), posing a global health challenge.
- Cellular senescence, marked by cell cycle arrest and a senescence-associated secretory phenotype (SASP), is a critical aging mechanism and therapeutic target.
- Dietary compounds fisetin and quercetin are being investigated for their senolytic and senomorphic properties.
Purpose of the Study:
- To review existing evidence on fisetin and quercetin's effects on senescence and SASP.
- To explore their potential in animal models and human studies related to aging and ARDs.
- To identify factors influencing the clinical translation of these nutrients.
Main Methods:
- Narrative literature review of studies on fisetin and quercetin.
- Analysis of data from animal models of aging and progeria.
- Examination of human interventional studies in geriatric syndromes and ARDs.
Main Results:
- Fisetin and quercetin demonstrate potential in modulating senescence and SASP biomarkers.
- Evidence from animal and human studies suggests therapeutic benefits.
- The review highlights the need to overcome barriers for clinical application.
Conclusions:
- Fisetin and quercetin show promise as senolytics and senomorphics for managing aging and ARDs.
- Further research and clinical translation are warranted to harness their full therapeutic potential.
- Understanding senescence mechanisms is key to developing effective interventions.
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