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Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells

The retinal pigment epithelium (RPE) is a densely pigmented, monostratified epithelium that provides metabolic and functional support to the outer segments of photoreceptors. Endogenous or exogenous oxidative stimuli determine a switch from physiological to pathological conditions, characterized by...

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Autores principales: Clementi, Maria Elisabetta, Maulucci, Giuseppe, Bianchetti, Giada, Pizzoferrato, Michela, Sampaolese, Beatrice, Tringali, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911437/
https://www.ncbi.nlm.nih.gov/pubmed/33572785
http://dx.doi.org/10.3390/antiox10020192
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author Clementi, Maria Elisabetta
Maulucci, Giuseppe
Bianchetti, Giada
Pizzoferrato, Michela
Sampaolese, Beatrice
Tringali, Giuseppe
author_facet Clementi, Maria Elisabetta
Maulucci, Giuseppe
Bianchetti, Giada
Pizzoferrato, Michela
Sampaolese, Beatrice
Tringali, Giuseppe
author_sort Clementi, Maria Elisabetta
collection PubMed
description The retinal pigment epithelium (RPE) is a densely pigmented, monostratified epithelium that provides metabolic and functional support to the outer segments of photoreceptors. Endogenous or exogenous oxidative stimuli determine a switch from physiological to pathological conditions, characterized by an increase of intracellular levels of reactive oxygen species (ROS). Accumulating evidence has elucidated that punicalagin (PUN), the major ellagitannin in pomegranate, is a potent antioxidant in several cell types. The present study aimed to investigate the protective effect of PUN on mitochondrial dysfunction associated with hydrogen peroxide (H(2)O(2))–induced oxidative stress. For this purpose, we used a human RPE cell line (ARPE–19) exposed to H(2)O(2) for 24 h. The effects of PUN pre–treatment (24 h) were examined on cell viability, mitochondrial ROS levels, mitochondrial membrane potential, and respiratory chain complexes, then finally on caspase–3 enzymatic activity. The results showed that supplementation with PUN: (a) significantly increased cell viability; (b) kept the mitochondrial membrane potential (ΔΨm) at healthy levels and limited ROS production; (c) preserved the activity of respiratory complexes; (d) reduced caspase–3 activity. In conclusion, due to its activity in helping mitochondrial functions, reducing oxidative stress, and subsequent induction of cellular apoptosis, PUN might be considered a useful nutraceutical agent in the treatment of oxidation–associated disorders of RPE.
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spelling pubmed-79114372021-02-28 Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells Clementi, Maria Elisabetta Maulucci, Giuseppe Bianchetti, Giada Pizzoferrato, Michela Sampaolese, Beatrice Tringali, Giuseppe Antioxidants (Basel) Article The retinal pigment epithelium (RPE) is a densely pigmented, monostratified epithelium that provides metabolic and functional support to the outer segments of photoreceptors. Endogenous or exogenous oxidative stimuli determine a switch from physiological to pathological conditions, characterized by an increase of intracellular levels of reactive oxygen species (ROS). Accumulating evidence has elucidated that punicalagin (PUN), the major ellagitannin in pomegranate, is a potent antioxidant in several cell types. The present study aimed to investigate the protective effect of PUN on mitochondrial dysfunction associated with hydrogen peroxide (H(2)O(2))–induced oxidative stress. For this purpose, we used a human RPE cell line (ARPE–19) exposed to H(2)O(2) for 24 h. The effects of PUN pre–treatment (24 h) were examined on cell viability, mitochondrial ROS levels, mitochondrial membrane potential, and respiratory chain complexes, then finally on caspase–3 enzymatic activity. The results showed that supplementation with PUN: (a) significantly increased cell viability; (b) kept the mitochondrial membrane potential (ΔΨm) at healthy levels and limited ROS production; (c) preserved the activity of respiratory complexes; (d) reduced caspase–3 activity. In conclusion, due to its activity in helping mitochondrial functions, reducing oxidative stress, and subsequent induction of cellular apoptosis, PUN might be considered a useful nutraceutical agent in the treatment of oxidation–associated disorders of RPE. MDPI 2021-01-29 /pmc/articles/PMC7911437/ /pubmed/33572785 http://dx.doi.org/10.3390/antiox10020192 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Clementi, Maria Elisabetta
Maulucci, Giuseppe
Bianchetti, Giada
Pizzoferrato, Michela
Sampaolese, Beatrice
Tringali, Giuseppe
Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells
title Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells
title_full Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells
title_fullStr Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells
title_full_unstemmed Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells
title_short Cytoprotective Effects of Punicalagin on Hydrogen–Peroxide–Mediated Oxidative Stress and Mitochondrial Dysfunction in Retinal Pigment Epithelium Cells
title_sort cytoprotective effects of punicalagin on hydrogen–peroxide–mediated oxidative stress and mitochondrial dysfunction in retinal pigment epithelium cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911437/
https://www.ncbi.nlm.nih.gov/pubmed/33572785
http://dx.doi.org/10.3390/antiox10020192
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