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Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease

SIRT1 is an NAD(+)-dependent class III histone deacetylase that is abundantly expressed in the kidney, where it modulates gene expression, apoptosis, energy homeostasis, autophagy, acute stress responses, and mitochondrial biogenesis. Alterations in SIRT1 activity and NAD(+) metabolism are frequentl...

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Detalles Bibliográficos
Autores principales: Tovar-Palacio, Claudia, Noriega, Lilia G., Mercado, Adriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837945/
https://www.ncbi.nlm.nih.gov/pubmed/35277012
http://dx.doi.org/10.3390/nu14030653
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author Tovar-Palacio, Claudia
Noriega, Lilia G.
Mercado, Adriana
author_facet Tovar-Palacio, Claudia
Noriega, Lilia G.
Mercado, Adriana
author_sort Tovar-Palacio, Claudia
collection PubMed
description SIRT1 is an NAD(+)-dependent class III histone deacetylase that is abundantly expressed in the kidney, where it modulates gene expression, apoptosis, energy homeostasis, autophagy, acute stress responses, and mitochondrial biogenesis. Alterations in SIRT1 activity and NAD(+) metabolism are frequently observed in acute and chronic kidney diseases of diverse origins, including obesity and diabetes. Nevertheless, in vitro and in vivo studies and clinical trials with humans show that the SIRT1-activating compounds derived from natural sources, such as polyphenols found in fruits, vegetables, and plants, including resveratrol, quercetin, and isoflavones, can prevent disease and be part of treatments for a wide variety of diseases. Here, we summarize the roles of SIRT1 and NAD(+) metabolism in renal pathophysiology and provide an overview of polyphenols that have the potential to restore SIRT1 and NAD(+) metabolism in renal diseases.
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spelling pubmed-88379452022-02-13 Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease Tovar-Palacio, Claudia Noriega, Lilia G. Mercado, Adriana Nutrients Review SIRT1 is an NAD(+)-dependent class III histone deacetylase that is abundantly expressed in the kidney, where it modulates gene expression, apoptosis, energy homeostasis, autophagy, acute stress responses, and mitochondrial biogenesis. Alterations in SIRT1 activity and NAD(+) metabolism are frequently observed in acute and chronic kidney diseases of diverse origins, including obesity and diabetes. Nevertheless, in vitro and in vivo studies and clinical trials with humans show that the SIRT1-activating compounds derived from natural sources, such as polyphenols found in fruits, vegetables, and plants, including resveratrol, quercetin, and isoflavones, can prevent disease and be part of treatments for a wide variety of diseases. Here, we summarize the roles of SIRT1 and NAD(+) metabolism in renal pathophysiology and provide an overview of polyphenols that have the potential to restore SIRT1 and NAD(+) metabolism in renal diseases. MDPI 2022-02-03 /pmc/articles/PMC8837945/ /pubmed/35277012 http://dx.doi.org/10.3390/nu14030653 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tovar-Palacio, Claudia
Noriega, Lilia G.
Mercado, Adriana
Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease
title Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease
title_full Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease
title_fullStr Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease
title_full_unstemmed Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease
title_short Potential of Polyphenols to Restore SIRT1 and NAD+ Metabolism in Renal Disease
title_sort potential of polyphenols to restore sirt1 and nad+ metabolism in renal disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837945/
https://www.ncbi.nlm.nih.gov/pubmed/35277012
http://dx.doi.org/10.3390/nu14030653
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