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Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages

Age-related injuries are often connected to alterations in redox homeostasis. The imbalance between free radical oxygen species and endogenous antioxidants defenses could be associated with a growing risk of transient ischemic attack and stroke. In this context, a daily supply of dietary antioxidant...

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Autores principales: Lonati, Elena, Carrozzini, Tatiana, Bruni, Ilaria, Mena, Pedro, Botto, Laura, Cazzaniga, Emanuela, Del Rio, Daniele, Labra, Massimo, Palestini, Paola, Bulbarelli, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839093/
https://www.ncbi.nlm.nih.gov/pubmed/35164314
http://dx.doi.org/10.3390/molecules27031049
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author Lonati, Elena
Carrozzini, Tatiana
Bruni, Ilaria
Mena, Pedro
Botto, Laura
Cazzaniga, Emanuela
Del Rio, Daniele
Labra, Massimo
Palestini, Paola
Bulbarelli, Alessandra
author_facet Lonati, Elena
Carrozzini, Tatiana
Bruni, Ilaria
Mena, Pedro
Botto, Laura
Cazzaniga, Emanuela
Del Rio, Daniele
Labra, Massimo
Palestini, Paola
Bulbarelli, Alessandra
author_sort Lonati, Elena
collection PubMed
description Age-related injuries are often connected to alterations in redox homeostasis. The imbalance between free radical oxygen species and endogenous antioxidants defenses could be associated with a growing risk of transient ischemic attack and stroke. In this context, a daily supply of dietary antioxidants could counteract oxidative stress occurring during ischemia/reperfusion injury (I/R), preventing brain damage. Here we investigated the potential antioxidant properties of coffee-derived circulating metabolites and a coffee pulp phytoextract, testing their efficacy as ROS scavengers in an in vitro model of ischemia. Indeed, the coffee fruit is an important source of phenolic compounds, such as chlorogenic acids, present both in the brewed seed and in the discarded pulp. Therefore, rat brain endothelial cells, subjected to oxygen and glucose deprivation (OGD) and recovery (ogR) to mimic reperfusion, were pretreated or not with coffee by-products. The results indicate that, under OGD/ogR, the ROS accumulation was reduced by coffee by-product. Additionally, the coffee extract activated the Nrf2 antioxidant pathway via Erk and Akt kinases phosphorylation, as shown by increased Nrf2 and HO-1 protein levels. The data indicate that the daily intake of coffee by-products as a dietary food supplement represents a potential nutritional strategy to counteract aging.
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spelling pubmed-88390932022-02-13 Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages Lonati, Elena Carrozzini, Tatiana Bruni, Ilaria Mena, Pedro Botto, Laura Cazzaniga, Emanuela Del Rio, Daniele Labra, Massimo Palestini, Paola Bulbarelli, Alessandra Molecules Article Age-related injuries are often connected to alterations in redox homeostasis. The imbalance between free radical oxygen species and endogenous antioxidants defenses could be associated with a growing risk of transient ischemic attack and stroke. In this context, a daily supply of dietary antioxidants could counteract oxidative stress occurring during ischemia/reperfusion injury (I/R), preventing brain damage. Here we investigated the potential antioxidant properties of coffee-derived circulating metabolites and a coffee pulp phytoextract, testing their efficacy as ROS scavengers in an in vitro model of ischemia. Indeed, the coffee fruit is an important source of phenolic compounds, such as chlorogenic acids, present both in the brewed seed and in the discarded pulp. Therefore, rat brain endothelial cells, subjected to oxygen and glucose deprivation (OGD) and recovery (ogR) to mimic reperfusion, were pretreated or not with coffee by-products. The results indicate that, under OGD/ogR, the ROS accumulation was reduced by coffee by-product. Additionally, the coffee extract activated the Nrf2 antioxidant pathway via Erk and Akt kinases phosphorylation, as shown by increased Nrf2 and HO-1 protein levels. The data indicate that the daily intake of coffee by-products as a dietary food supplement represents a potential nutritional strategy to counteract aging. MDPI 2022-02-03 /pmc/articles/PMC8839093/ /pubmed/35164314 http://dx.doi.org/10.3390/molecules27031049 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 Article
Lonati, Elena
Carrozzini, Tatiana
Bruni, Ilaria
Mena, Pedro
Botto, Laura
Cazzaniga, Emanuela
Del Rio, Daniele
Labra, Massimo
Palestini, Paola
Bulbarelli, Alessandra
Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages
title Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages
title_full Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages
title_fullStr Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages
title_full_unstemmed Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages
title_short Coffee-Derived Phenolic Compounds Activate Nrf2 Antioxidant Pathway in I/R Injury In Vitro Model: A Nutritional Approach Preventing Age Related-Damages
title_sort coffee-derived phenolic compounds activate nrf2 antioxidant pathway in i/r injury in vitro model: a nutritional approach preventing age related-damages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8839093/
https://www.ncbi.nlm.nih.gov/pubmed/35164314
http://dx.doi.org/10.3390/molecules27031049
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