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Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress
Aging is a process characterised by a general decline in physiological functions. The high bioavailability of reactive oxygen species (ROS) plays an important role in the aging rate. Due to the close relationship between aging and oxidative stress (OS), functional foods rich in flavonoids are excell...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368007/ https://www.ncbi.nlm.nih.gov/pubmed/35954235 http://dx.doi.org/10.3390/cells11152391 |
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author | Remigante, Alessia Spinelli, Sara Straface, Elisabetta Gambardella, Lucrezia Caruso, Daniele Falliti, Giuseppe Dossena, Silvia Marino, Angela Morabito, Rossana |
author_facet | Remigante, Alessia Spinelli, Sara Straface, Elisabetta Gambardella, Lucrezia Caruso, Daniele Falliti, Giuseppe Dossena, Silvia Marino, Angela Morabito, Rossana |
author_sort | Remigante, Alessia |
collection | PubMed |
description | Aging is a process characterised by a general decline in physiological functions. The high bioavailability of reactive oxygen species (ROS) plays an important role in the aging rate. Due to the close relationship between aging and oxidative stress (OS), functional foods rich in flavonoids are excellent candidates to counteract age-related changes. This study aimed to verify the protective role of Açaì extract in a d-Galactose (d-Gal)-induced model of aging in human erythrocytes. Markers of OS, including ROS production, thiobarbituric acid reactive substances (TBARS) levels, oxidation of protein sulfhydryl groups, as well as the anion exchange capability through Band 3 protein (B3p) and glycated haemoglobin (A1c) have been analysed in erythrocytes treated with d-Gal for 24 h, with or without pre-incubation for 1 h with 0.5–10 µg/mL Açaì extract. Our results show that the extract avoided the formation of acanthocytes and leptocytes observed after exposure to 50 and 100 mM d-Gal, respectively, prevented d-Gal-induced OS damage, and restored alterations in the distribution of B3p and CD47 proteins. Interestingly, d-Gal exposure was associated with an acceleration of the rate constant of SO(4)(2−) uptake through B3p, as well as A1c formation. Both alterations have been attenuated by pre-treatment with the Açaì extract. These findings contribute to clarify the aging mechanisms in human erythrocytes and propose functional foods rich in flavonoids as natural antioxidants for the treatment and prevention of OS-related disease conditions. |
format | Online Article Text |
id | pubmed-9368007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93680072022-08-12 Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress Remigante, Alessia Spinelli, Sara Straface, Elisabetta Gambardella, Lucrezia Caruso, Daniele Falliti, Giuseppe Dossena, Silvia Marino, Angela Morabito, Rossana Cells Article Aging is a process characterised by a general decline in physiological functions. The high bioavailability of reactive oxygen species (ROS) plays an important role in the aging rate. Due to the close relationship between aging and oxidative stress (OS), functional foods rich in flavonoids are excellent candidates to counteract age-related changes. This study aimed to verify the protective role of Açaì extract in a d-Galactose (d-Gal)-induced model of aging in human erythrocytes. Markers of OS, including ROS production, thiobarbituric acid reactive substances (TBARS) levels, oxidation of protein sulfhydryl groups, as well as the anion exchange capability through Band 3 protein (B3p) and glycated haemoglobin (A1c) have been analysed in erythrocytes treated with d-Gal for 24 h, with or without pre-incubation for 1 h with 0.5–10 µg/mL Açaì extract. Our results show that the extract avoided the formation of acanthocytes and leptocytes observed after exposure to 50 and 100 mM d-Gal, respectively, prevented d-Gal-induced OS damage, and restored alterations in the distribution of B3p and CD47 proteins. Interestingly, d-Gal exposure was associated with an acceleration of the rate constant of SO(4)(2−) uptake through B3p, as well as A1c formation. Both alterations have been attenuated by pre-treatment with the Açaì extract. These findings contribute to clarify the aging mechanisms in human erythrocytes and propose functional foods rich in flavonoids as natural antioxidants for the treatment and prevention of OS-related disease conditions. MDPI 2022-08-03 /pmc/articles/PMC9368007/ /pubmed/35954235 http://dx.doi.org/10.3390/cells11152391 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 Remigante, Alessia Spinelli, Sara Straface, Elisabetta Gambardella, Lucrezia Caruso, Daniele Falliti, Giuseppe Dossena, Silvia Marino, Angela Morabito, Rossana Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress |
title | Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress |
title_full | Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress |
title_fullStr | Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress |
title_full_unstemmed | Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress |
title_short | Açaì (Euterpe oleracea) Extract Protects Human Erythrocytes from Age-Related Oxidative Stress |
title_sort | açaì (euterpe oleracea) extract protects human erythrocytes from age-related oxidative stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368007/ https://www.ncbi.nlm.nih.gov/pubmed/35954235 http://dx.doi.org/10.3390/cells11152391 |
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