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  • 1 Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, USA; Department of Neuroscience, University of Parma Medical School, 43100 Parma, Italy.
  • 2 Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, USA.
  • 3 Department of Neuroscience, University of Parma Medical School, 43100 Parma, Italy.
  • 1 Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, USA; Department of Neuroscience, University of Parma Medical School, 43100 Parma, Italy.
  • 2 Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, USA.
  • 3 Department of Neuroscience, University of Parma Medical School, 43100 Parma, Italy.
  • Increasing interest has recently focused on determining whether several natural compounds, collectively referred to as nutraceuticals, may exert neuroprotective actions in the developing, adult, and aging nervous system. Quercetin, a polyphenol widely present in nature, has received the most attention in this regard. Several studies in vitro, in experimental animals and in humans, have provided supportive evidence for neuroprotective effects of quercetin, either against neurotoxic chemicals or in various models of neuronal injury and neurodegenerative diseases. The exact mechanisms of such protective effects remain elusive, though many hypotheses have been formulated. In addition to a possible direct antioxidant effect, quercetin may also act by stimulating cellular defenses against oxidative stress. Two such pathways include the induction of Nrf2-ARE and induction of the antioxidant/anti-inflammatory enzyme paraoxonase 2 (PON2). In addition, quercetin has been shown to activate sirtuins (SIRT1), to induce autophagy, and to act as a phytoestrogen, all mechanisms by which quercetin may provide its neuroprotection. Acıkara OB, et al. CNS Neurol Disord Drug Targets. 2022;21(9):795-817. doi: 10.2174/1871527320666211206122407. CNS Neurol Disord Drug Targets. 2022. PMID: 34872486 Grewal AK, et al. Biomed Pharmacother. 2021 Aug;140:111729. doi: 10.1016/j.biopha.2021.111729. Epub 2021 May 25. Biomed Pharmacother. 2021. PMID: 34044274 Costa LG, et al. Neurochem Res. 2013 Sep;38(9):1809-18. doi: 10.1007/s11064-013-1085-1. Epub 2013 Jun 7. Neurochem Res. 2013. PMID: 23743621 Free PMC article. Pandey AK, et al. Int Rev Neurobiol. 2012;102:107-46. doi: 10.1016/B978-0-12-386986-9.00005-3. Int Rev Neurobiol. 2012. PMID: 22748828 Arredondo F, et al. Free Radic Biol Med. 2010 Sep 1;49(5):738-47. doi: 10.1016/j.freeradbiomed.2010.05.020. Epub 2010 Jun 8. Free Radic Biol Med. 2010. PMID: 20554019 Arozal W, et al. ScientificWorldJournal. 2024 Apr 9;2024:8034401. doi: 10.1155/2024/8034401. eCollection 2024. ScientificWorldJournal. 2024. PMID: 38633104 Free PMC article. Abdallah AE. RSC Adv. 2024 Apr 5;14(16):11057-11088. doi: 10.1039/d3ra08333k. eCollection 2024 Apr 3. RSC Adv. 2024. PMID: 38586442 Free PMC article. Review. Mavrogonatou E, et al. Metabolites. 2024 Feb 28;14(3):146. doi: 10.3390/metabo14030146. Metabolites. 2024. PMID: 38535306 Free PMC article. Review. Zúñiga-Hernández SR, et al. Nutrients. 2024 Feb 19;16(4):566. doi: 10.3390/nu16040566. Nutrients. 2024. PMID: 38398890 Free PMC article. Harwood M., Danielewska-Nikiel B., Borzelleca J. F., Flamm G. W., Williams G. M., Lines T. C. A critical review of the data related to the safety of quercetin and lack of evidence of in vivo toxicity, including lack of genotoxic/carcinogenic properties. Food and Chemical Toxicology. 2007;45(11):2179–2205. doi: 10.1016/j.fct.2007.05.015.