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Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation

INTRODUCTION: Skin aging is a normal process that might be accelerated or delayed by altering the balance between antioxidants and free radicals due to increase in the exposure to reactive oxygen species (ROS) into skin cells via UV radiation. Antioxidants can neutralize the harmful effects of ROS,...

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Autores principales: Mohamad, Ebtesam A, Aly, Aya A, Khalaf, Aya A, Ahmed, Mona I, Kamel, Reham M, Abdelnaby, Sherouk M, Abdelzaher, Yasmine H, Sedrak, Marize G, Mousa, Shaker A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311472/
https://www.ncbi.nlm.nih.gov/pubmed/34321865
http://dx.doi.org/10.2147/DDDT.S316247
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author Mohamad, Ebtesam A
Aly, Aya A
Khalaf, Aya A
Ahmed, Mona I
Kamel, Reham M
Abdelnaby, Sherouk M
Abdelzaher, Yasmine H
Sedrak, Marize G
Mousa, Shaker A
author_facet Mohamad, Ebtesam A
Aly, Aya A
Khalaf, Aya A
Ahmed, Mona I
Kamel, Reham M
Abdelnaby, Sherouk M
Abdelzaher, Yasmine H
Sedrak, Marize G
Mousa, Shaker A
author_sort Mohamad, Ebtesam A
collection PubMed
description INTRODUCTION: Skin aging is a normal process that might be accelerated or delayed by altering the balance between antioxidants and free radicals due to increase in the exposure to reactive oxygen species (ROS) into skin cells via UV radiation. Antioxidants can neutralize the harmful effects of ROS, and secondary plant metabolites might help protect against UV radiation. METHODS: In this study, punicalagin was extracted from pomegranate, and concentrations of total polyphenolics and flavonoids were determined, and antioxidant activities were measured. Punicalagin was loaded onto niosomes, and its morphology and release were studied. An in vitro study was performed on human fibroblast cell line HFB4 cells with aging induced by H(2)O(2) and UV radiation. Cell cycle arrest was studied, and different genes (MMP3, Col1A1, Timp3, and TERT) involved in the skin aging process were selected to measure punicalagin’s effect. RESULTS: Punicalagin succeeded in reducing the growth arrest of HFB4 cells, activated production of the Col1A1 and Timp3 genes, maintained collagen level, and lowered MMP3. Punicalagin increased human TERT concentration in skin cells. DISCUSSION: Punicalagin is promising as a natural antioxidant to protect human skin from aging.
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spelling pubmed-83114722021-07-27 Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation Mohamad, Ebtesam A Aly, Aya A Khalaf, Aya A Ahmed, Mona I Kamel, Reham M Abdelnaby, Sherouk M Abdelzaher, Yasmine H Sedrak, Marize G Mousa, Shaker A Drug Des Devel Ther Original Research INTRODUCTION: Skin aging is a normal process that might be accelerated or delayed by altering the balance between antioxidants and free radicals due to increase in the exposure to reactive oxygen species (ROS) into skin cells via UV radiation. Antioxidants can neutralize the harmful effects of ROS, and secondary plant metabolites might help protect against UV radiation. METHODS: In this study, punicalagin was extracted from pomegranate, and concentrations of total polyphenolics and flavonoids were determined, and antioxidant activities were measured. Punicalagin was loaded onto niosomes, and its morphology and release were studied. An in vitro study was performed on human fibroblast cell line HFB4 cells with aging induced by H(2)O(2) and UV radiation. Cell cycle arrest was studied, and different genes (MMP3, Col1A1, Timp3, and TERT) involved in the skin aging process were selected to measure punicalagin’s effect. RESULTS: Punicalagin succeeded in reducing the growth arrest of HFB4 cells, activated production of the Col1A1 and Timp3 genes, maintained collagen level, and lowered MMP3. Punicalagin increased human TERT concentration in skin cells. DISCUSSION: Punicalagin is promising as a natural antioxidant to protect human skin from aging. Dove 2021-07-17 /pmc/articles/PMC8311472/ /pubmed/34321865 http://dx.doi.org/10.2147/DDDT.S316247 Text en © 2021 Mohamad et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Mohamad, Ebtesam A
Aly, Aya A
Khalaf, Aya A
Ahmed, Mona I
Kamel, Reham M
Abdelnaby, Sherouk M
Abdelzaher, Yasmine H
Sedrak, Marize G
Mousa, Shaker A
Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation
title Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation
title_full Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation
title_fullStr Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation
title_full_unstemmed Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation
title_short Evaluation of Natural Bioactive-Derived Punicalagin Niosomes in Skin-Aging Processes Accelerated by Oxidant and Ultraviolet Radiation
title_sort evaluation of natural bioactive-derived punicalagin niosomes in skin-aging processes accelerated by oxidant and ultraviolet radiation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311472/
https://www.ncbi.nlm.nih.gov/pubmed/34321865
http://dx.doi.org/10.2147/DDDT.S316247
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