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Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane
Significance: Side effects of many cancer treatments are associated with the production of reactive oxygen species (ROS) in normal tissues. This explains why patients treated by photodynamic therapy (PDT) often suffer from skin photosensitization, whereas those subject to radiotherapies frequently e...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013152/ https://www.ncbi.nlm.nih.gov/pubmed/32052612 http://dx.doi.org/10.1117/1.JBO.25.6.063807 |
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author | Joniová, Jaroslava Wagnières, Georges |
author_facet | Joniová, Jaroslava Wagnières, Georges |
author_sort | Joniová, Jaroslava |
collection | PubMed |
description | Significance: Side effects of many cancer treatments are associated with the production of reactive oxygen species (ROS) in normal tissues. This explains why patients treated by photodynamic therapy (PDT) often suffer from skin photosensitization, whereas those subject to radiotherapies frequently experience damages in various organs, including the skin. Aim: Catechin, which belongs to the natural flavanols family, is well known for its antioxidant properties. Hence, our main objective was to investigate whether catechin can reduce damages induced by PDT using protoporphyrin IX (PpIX-PDT), an endogenous photosensitizer commonly used in dermatology. Approach: An in vivo model, the chick embryo chorioallantoic membrane (CAM), was used for this study. An amount of [Formula: see text] of a solution containing 5-aminolevulinic acid, a natural precursor of PpIX, was applied topically on the CAM 4 h before PDTs (405 nm, [Formula: see text] , [Formula: see text]). Catechin was applied at different concentrations (1 to [Formula: see text]) and times (0 to 240 min) before PDT. In addition, we assessed the potency of catechin to reduce the PpIX fluorescence photobleaching induced by PDT. Results: We observed that catechin significantly reduces the vascular damages generated by PpIX-PDT. Moreover, we have shown that catechin inhibits PpIX photobleaching. Conclusions: These observations suggest that catechin significantly reduces the level of ROS produced by PpIX-PDT. |
format | Online Article Text |
id | pubmed-7013152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-70131522020-02-14 Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane Joniová, Jaroslava Wagnières, Georges J Biomed Opt Special Section on Photodynamic Therapy Significance: Side effects of many cancer treatments are associated with the production of reactive oxygen species (ROS) in normal tissues. This explains why patients treated by photodynamic therapy (PDT) often suffer from skin photosensitization, whereas those subject to radiotherapies frequently experience damages in various organs, including the skin. Aim: Catechin, which belongs to the natural flavanols family, is well known for its antioxidant properties. Hence, our main objective was to investigate whether catechin can reduce damages induced by PDT using protoporphyrin IX (PpIX-PDT), an endogenous photosensitizer commonly used in dermatology. Approach: An in vivo model, the chick embryo chorioallantoic membrane (CAM), was used for this study. An amount of [Formula: see text] of a solution containing 5-aminolevulinic acid, a natural precursor of PpIX, was applied topically on the CAM 4 h before PDTs (405 nm, [Formula: see text] , [Formula: see text]). Catechin was applied at different concentrations (1 to [Formula: see text]) and times (0 to 240 min) before PDT. In addition, we assessed the potency of catechin to reduce the PpIX fluorescence photobleaching induced by PDT. Results: We observed that catechin significantly reduces the vascular damages generated by PpIX-PDT. Moreover, we have shown that catechin inhibits PpIX photobleaching. Conclusions: These observations suggest that catechin significantly reduces the level of ROS produced by PpIX-PDT. Society of Photo-Optical Instrumentation Engineers 2020-02-12 2020-06 /pmc/articles/PMC7013152/ /pubmed/32052612 http://dx.doi.org/10.1117/1.JBO.25.6.063807 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/ Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Special Section on Photodynamic Therapy Joniová, Jaroslava Wagnières, Georges Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane |
title | Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane |
title_full | Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane |
title_fullStr | Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane |
title_full_unstemmed | Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane |
title_short | Catechin reduces phototoxic effects induced by protoporphyrin IX-based photodynamic therapy in the chick embryo chorioallantoic membrane |
title_sort | catechin reduces phototoxic effects induced by protoporphyrin ix-based photodynamic therapy in the chick embryo chorioallantoic membrane |
topic | Special Section on Photodynamic Therapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013152/ https://www.ncbi.nlm.nih.gov/pubmed/32052612 http://dx.doi.org/10.1117/1.JBO.25.6.063807 |
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