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Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism

Quercetin, a naturally non-toxic flavonoid within the safe dose range with antioxidant, anti-apoptotic and anti-inflammatory properties, plays an important role in the treatment of aging-related diseases. Sirtuin 1 (SIRT1), a member of NAD(+)-dependent deacetylase enzyme family, is extensively explo...

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Autores principales: Cui, Zhifu, Zhao, Xingtao, Amevor, Felix Kwame, Du, Xiaxia, Wang, Yan, Li, Diyan, Shu, Gang, Tian, Yaofu, Zhao, Xiaoling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355713/
https://www.ncbi.nlm.nih.gov/pubmed/35935939
http://dx.doi.org/10.3389/fimmu.2022.943321
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author Cui, Zhifu
Zhao, Xingtao
Amevor, Felix Kwame
Du, Xiaxia
Wang, Yan
Li, Diyan
Shu, Gang
Tian, Yaofu
Zhao, Xiaoling
author_facet Cui, Zhifu
Zhao, Xingtao
Amevor, Felix Kwame
Du, Xiaxia
Wang, Yan
Li, Diyan
Shu, Gang
Tian, Yaofu
Zhao, Xiaoling
author_sort Cui, Zhifu
collection PubMed
description Quercetin, a naturally non-toxic flavonoid within the safe dose range with antioxidant, anti-apoptotic and anti-inflammatory properties, plays an important role in the treatment of aging-related diseases. Sirtuin 1 (SIRT1), a member of NAD(+)-dependent deacetylase enzyme family, is extensively explored as a potential therapeutic target for attenuating aging-induced disorders. SIRT1 possess beneficial effects against aging-related diseases such as Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD), Depression, Osteoporosis, Myocardial ischemia (M/I) and reperfusion (MI/R), Atherosclerosis (AS), and Diabetes. Previous studies have reported that aging increases tissue susceptibility, whereas, SIRT1 regulates cellular senescence and multiple aging-related cellular processes, including SIRT1/Keap1/Nrf2/HO-1 and SIRTI/PI3K/Akt/GSK-3β mediated oxidative stress, SIRT1/NF-κB and SIRT1/NLRP3 regulated inflammatory response, SIRT1/PGC1α/eIF2α/ATF4/CHOP and SIRT1/PKD1/CREB controlled phosphorylation, SIRT1-PINK1-Parkin mediated mitochondrial damage, SIRT1/FoxO mediated autophagy, and SIRT1/FoxG1/CREB/BDNF/Trkβ-catenin mediated neuroprotective effects. In this review, we summarized the role of SIRT1 in the improvement of the attenuation effect of quercetin on aging-related diseases and the relationship between relevant signaling pathways regulated by SIRT1. Moreover, the functional regulation of quercetin in aging-related markers such as oxidative stress, inflammatory response, mitochondrial function, autophagy and apoptosis through SIRT1 was discussed. Finally, the prospects of an extracellular vesicles (EVs) as quercetin loading and delivery, and SIRT1-mediated EVs as signal carriers for treating aging-related diseases, as well as discussed the ferroptosis alleviation effects of quercetin to protect against aging-related disease via activating SIRT1. Generally, SIRT1 may serve as a promising therapeutic target in the treatment of aging-related diseases via inhibiting oxidative stress, reducing inflammatory responses, and restoring mitochondrial dysfunction.
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spelling pubmed-93557132022-08-06 Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism Cui, Zhifu Zhao, Xingtao Amevor, Felix Kwame Du, Xiaxia Wang, Yan Li, Diyan Shu, Gang Tian, Yaofu Zhao, Xiaoling Front Immunol Immunology Quercetin, a naturally non-toxic flavonoid within the safe dose range with antioxidant, anti-apoptotic and anti-inflammatory properties, plays an important role in the treatment of aging-related diseases. Sirtuin 1 (SIRT1), a member of NAD(+)-dependent deacetylase enzyme family, is extensively explored as a potential therapeutic target for attenuating aging-induced disorders. SIRT1 possess beneficial effects against aging-related diseases such as Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD), Depression, Osteoporosis, Myocardial ischemia (M/I) and reperfusion (MI/R), Atherosclerosis (AS), and Diabetes. Previous studies have reported that aging increases tissue susceptibility, whereas, SIRT1 regulates cellular senescence and multiple aging-related cellular processes, including SIRT1/Keap1/Nrf2/HO-1 and SIRTI/PI3K/Akt/GSK-3β mediated oxidative stress, SIRT1/NF-κB and SIRT1/NLRP3 regulated inflammatory response, SIRT1/PGC1α/eIF2α/ATF4/CHOP and SIRT1/PKD1/CREB controlled phosphorylation, SIRT1-PINK1-Parkin mediated mitochondrial damage, SIRT1/FoxO mediated autophagy, and SIRT1/FoxG1/CREB/BDNF/Trkβ-catenin mediated neuroprotective effects. In this review, we summarized the role of SIRT1 in the improvement of the attenuation effect of quercetin on aging-related diseases and the relationship between relevant signaling pathways regulated by SIRT1. Moreover, the functional regulation of quercetin in aging-related markers such as oxidative stress, inflammatory response, mitochondrial function, autophagy and apoptosis through SIRT1 was discussed. Finally, the prospects of an extracellular vesicles (EVs) as quercetin loading and delivery, and SIRT1-mediated EVs as signal carriers for treating aging-related diseases, as well as discussed the ferroptosis alleviation effects of quercetin to protect against aging-related disease via activating SIRT1. Generally, SIRT1 may serve as a promising therapeutic target in the treatment of aging-related diseases via inhibiting oxidative stress, reducing inflammatory responses, and restoring mitochondrial dysfunction. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9355713/ /pubmed/35935939 http://dx.doi.org/10.3389/fimmu.2022.943321 Text en Copyright © 2022 Cui, Zhao, Amevor, Du, Wang, Li, Shu, Tian and Zhao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Cui, Zhifu
Zhao, Xingtao
Amevor, Felix Kwame
Du, Xiaxia
Wang, Yan
Li, Diyan
Shu, Gang
Tian, Yaofu
Zhao, Xiaoling
Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism
title Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism
title_full Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism
title_fullStr Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism
title_full_unstemmed Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism
title_short Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism
title_sort therapeutic application of quercetin in aging-related diseases: sirt1 as a potential mechanism
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355713/
https://www.ncbi.nlm.nih.gov/pubmed/35935939
http://dx.doi.org/10.3389/fimmu.2022.943321
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