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Protective effect of different antioxidant agents in UVB-irradiated keratinocytes
Skin cells can respond to UVB-induced damage either by tolerating it, or restoring it through antioxidant activation and DNA repair mechanisms or, ultimately, undergoing programmed cell death, when damage is massive. Nutritional factors, in particular, food antioxidants, have attracted much interest...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617901/ https://www.ncbi.nlm.nih.gov/pubmed/29046052 http://dx.doi.org/10.4081/ejh.2017.2784 |
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author | Salucci, Sara Burattini, Sabrina Buontempo, Francesca Martelli, Alberto Maria Falcieri, Elisabetta Battistelli, Michela |
author_facet | Salucci, Sara Burattini, Sabrina Buontempo, Francesca Martelli, Alberto Maria Falcieri, Elisabetta Battistelli, Michela |
author_sort | Salucci, Sara |
collection | PubMed |
description | Skin cells can respond to UVB-induced damage either by tolerating it, or restoring it through antioxidant activation and DNA repair mechanisms or, ultimately, undergoing programmed cell death, when damage is massive. Nutritional factors, in particular, food antioxidants, have attracted much interest because of their potential use in new preventive, protective, and therapeutic strategies for chronic degenerative diseases, including skin inflammation and cancer. Some polyphenols, present in virgin olive oil, well tolerated by organism after oral administration, show a variety of pharmacological and clinical benefits such as antioxidant, anti-cancer, anti-inflammatory, and neuro-protective activities. Here, the protective effects of antioxidant compounds against UV-induced apoptosis have been described in HaCaT cell line. Human keratinocytes were pre-treated with antioxidants before UVB exposure and their effects have been evaluated by means of ultrastructural analyses. After UVB radiation, a known cell death trigger, typical apoptotic features, absent in control condition and in antioxidant alone-treated cells, appear. An evident numerical decrease of ultrastructural apoptotic patterns and TUNEL positive nuclei can be observed when natural antioxidants were supplied before cell death induction. These data have been confirmed by molecular investigation of caspase activity. In conclusion, this paper highlights antioxidant compound ability to prevent apoptotic cell death in human keratinocytes exposed to UVB, suggesting, for these molecules, a potential role in preventing skin damage. |
format | Online Article Text |
id | pubmed-5617901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-56179012017-10-02 Protective effect of different antioxidant agents in UVB-irradiated keratinocytes Salucci, Sara Burattini, Sabrina Buontempo, Francesca Martelli, Alberto Maria Falcieri, Elisabetta Battistelli, Michela Eur J Histochem Original Paper Skin cells can respond to UVB-induced damage either by tolerating it, or restoring it through antioxidant activation and DNA repair mechanisms or, ultimately, undergoing programmed cell death, when damage is massive. Nutritional factors, in particular, food antioxidants, have attracted much interest because of their potential use in new preventive, protective, and therapeutic strategies for chronic degenerative diseases, including skin inflammation and cancer. Some polyphenols, present in virgin olive oil, well tolerated by organism after oral administration, show a variety of pharmacological and clinical benefits such as antioxidant, anti-cancer, anti-inflammatory, and neuro-protective activities. Here, the protective effects of antioxidant compounds against UV-induced apoptosis have been described in HaCaT cell line. Human keratinocytes were pre-treated with antioxidants before UVB exposure and their effects have been evaluated by means of ultrastructural analyses. After UVB radiation, a known cell death trigger, typical apoptotic features, absent in control condition and in antioxidant alone-treated cells, appear. An evident numerical decrease of ultrastructural apoptotic patterns and TUNEL positive nuclei can be observed when natural antioxidants were supplied before cell death induction. These data have been confirmed by molecular investigation of caspase activity. In conclusion, this paper highlights antioxidant compound ability to prevent apoptotic cell death in human keratinocytes exposed to UVB, suggesting, for these molecules, a potential role in preventing skin damage. PAGEPress Publications, Pavia, Italy 2017-09-18 /pmc/articles/PMC5617901/ /pubmed/29046052 http://dx.doi.org/10.4081/ejh.2017.2784 Text en ©Copyright S. Salucci et al., 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Paper Salucci, Sara Burattini, Sabrina Buontempo, Francesca Martelli, Alberto Maria Falcieri, Elisabetta Battistelli, Michela Protective effect of different antioxidant agents in UVB-irradiated keratinocytes |
title | Protective effect of different antioxidant agents in UVB-irradiated keratinocytes |
title_full | Protective effect of different antioxidant agents in UVB-irradiated keratinocytes |
title_fullStr | Protective effect of different antioxidant agents in UVB-irradiated keratinocytes |
title_full_unstemmed | Protective effect of different antioxidant agents in UVB-irradiated keratinocytes |
title_short | Protective effect of different antioxidant agents in UVB-irradiated keratinocytes |
title_sort | protective effect of different antioxidant agents in uvb-irradiated keratinocytes |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617901/ https://www.ncbi.nlm.nih.gov/pubmed/29046052 http://dx.doi.org/10.4081/ejh.2017.2784 |
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