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Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells

Introduction: Aging is a process characterised by a decline in physiological functions. Reactive species play a crucial role in the aging rate. Due to the close relationship between aging and oxidative stress, functional foods rich in phytochemicals are excellent candidates to neutralise age-related...

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Autores principales: Remigante, Alessia, Spinelli, Sara, Straface, Elisabetta, Gambardella, Lucrezia, Russo, Marina, Cafeo, Giovanna, Caruso, Daniele, Falliti, Giuseppe, Dugo, Paola, Dossena, Silvia, Marino, Angela, Morabito, Rossana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348362/
https://www.ncbi.nlm.nih.gov/pubmed/37457030
http://dx.doi.org/10.3389/fphys.2023.1225552
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author Remigante, Alessia
Spinelli, Sara
Straface, Elisabetta
Gambardella, Lucrezia
Russo, Marina
Cafeo, Giovanna
Caruso, Daniele
Falliti, Giuseppe
Dugo, Paola
Dossena, Silvia
Marino, Angela
Morabito, Rossana
author_facet Remigante, Alessia
Spinelli, Sara
Straface, Elisabetta
Gambardella, Lucrezia
Russo, Marina
Cafeo, Giovanna
Caruso, Daniele
Falliti, Giuseppe
Dugo, Paola
Dossena, Silvia
Marino, Angela
Morabito, Rossana
author_sort Remigante, Alessia
collection PubMed
description Introduction: Aging is a process characterised by a decline in physiological functions. Reactive species play a crucial role in the aging rate. Due to the close relationship between aging and oxidative stress, functional foods rich in phytochemicals are excellent candidates to neutralise age-related changes. Aim: This investigation aims to verify the potential protective role of bergamot (Citrus bergamia, Femminello cultivar) peel and juice extract in a model of aging represented by human red blood cells (RBCs) exposed to D-Galactose (DGal). Methods: Bergamot peel and juice extracts were subjected to RP-HPLC/PDA/MS for determination of their composition in bioactive compounds. Markers of oxidative stress, including ROS production, thiobarbituric acid reactive substances (TBARS) levels -a marker of lipid peroxidation, oxidation of total protein sulfhydryl groups, as well as the expression and anion exchange capability of band 3 and glycated haemoglobin (A1c) production have been investigated in RBCs treated with D-Gal for 24 h, with or without pre-incubation for 15 min with 5 μg/mL peel or juice extract. In addition, the activity of the endogenous antioxidant system, including catalase (CAT) and superoxide dismutase (SOD), as well as the diversion of the RBC metabolism from glycolysis towards the pentose phosphate pathway shunt, as denoted by activation of glucose-6-phosphate dehydrogenase (G6PDH), have been explored. Results: Data shown here suggest that bergamot peel and juice extract i) prevented the D-Gal-induced ROS production, and consequently, oxidative stress injury to biological macromolecules including membrane lipids and proteins; ii) significantly restored D-Gal-induced alterations in the distribution and ion transport kinetics of band 3; iii) blunted A1c production; iv) effectively impeded the over-activation of the endogenous antioxidant enzymes CAT and SOD; and v) significantly prevented the activation of G6PDH. Discussion: These results further contribute to shed light on aging mechanisms in human RBCs and identify bergamot as a functional food rich in natural antioxidants useful for prevention and treatment of oxidative stress-related changes, which may lead to pathological states during aging.
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spelling pubmed-103483622023-07-15 Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells Remigante, Alessia Spinelli, Sara Straface, Elisabetta Gambardella, Lucrezia Russo, Marina Cafeo, Giovanna Caruso, Daniele Falliti, Giuseppe Dugo, Paola Dossena, Silvia Marino, Angela Morabito, Rossana Front Physiol Physiology Introduction: Aging is a process characterised by a decline in physiological functions. Reactive species play a crucial role in the aging rate. Due to the close relationship between aging and oxidative stress, functional foods rich in phytochemicals are excellent candidates to neutralise age-related changes. Aim: This investigation aims to verify the potential protective role of bergamot (Citrus bergamia, Femminello cultivar) peel and juice extract in a model of aging represented by human red blood cells (RBCs) exposed to D-Galactose (DGal). Methods: Bergamot peel and juice extracts were subjected to RP-HPLC/PDA/MS for determination of their composition in bioactive compounds. Markers of oxidative stress, including ROS production, thiobarbituric acid reactive substances (TBARS) levels -a marker of lipid peroxidation, oxidation of total protein sulfhydryl groups, as well as the expression and anion exchange capability of band 3 and glycated haemoglobin (A1c) production have been investigated in RBCs treated with D-Gal for 24 h, with or without pre-incubation for 15 min with 5 μg/mL peel or juice extract. In addition, the activity of the endogenous antioxidant system, including catalase (CAT) and superoxide dismutase (SOD), as well as the diversion of the RBC metabolism from glycolysis towards the pentose phosphate pathway shunt, as denoted by activation of glucose-6-phosphate dehydrogenase (G6PDH), have been explored. Results: Data shown here suggest that bergamot peel and juice extract i) prevented the D-Gal-induced ROS production, and consequently, oxidative stress injury to biological macromolecules including membrane lipids and proteins; ii) significantly restored D-Gal-induced alterations in the distribution and ion transport kinetics of band 3; iii) blunted A1c production; iv) effectively impeded the over-activation of the endogenous antioxidant enzymes CAT and SOD; and v) significantly prevented the activation of G6PDH. Discussion: These results further contribute to shed light on aging mechanisms in human RBCs and identify bergamot as a functional food rich in natural antioxidants useful for prevention and treatment of oxidative stress-related changes, which may lead to pathological states during aging. Frontiers Media S.A. 2023-06-30 /pmc/articles/PMC10348362/ /pubmed/37457030 http://dx.doi.org/10.3389/fphys.2023.1225552 Text en Copyright © 2023 Remigante, Spinelli, Straface, Gambardella, Russo, Cafeo, Caruso, Falliti, Dugo, Dossena, Marino and Morabito. 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 Physiology
Remigante, Alessia
Spinelli, Sara
Straface, Elisabetta
Gambardella, Lucrezia
Russo, Marina
Cafeo, Giovanna
Caruso, Daniele
Falliti, Giuseppe
Dugo, Paola
Dossena, Silvia
Marino, Angela
Morabito, Rossana
Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells
title Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells
title_full Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells
title_fullStr Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells
title_full_unstemmed Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells
title_short Mechanisms underlying the anti-aging activity of bergamot (Citrus bergamia) extract in human red blood cells
title_sort mechanisms underlying the anti-aging activity of bergamot (citrus bergamia) extract in human red blood cells
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348362/
https://www.ncbi.nlm.nih.gov/pubmed/37457030
http://dx.doi.org/10.3389/fphys.2023.1225552
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