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Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study

PURPOSE: Radiation-induced oral mucositis limits the delivery of high-dose radiation to head and neck cancer. This study investigated the effectiveness of epicatechin (EC), a component of green tea extracts, on radiation-induced oral mucositis in vitro and in vivo. EXPERIMENTAL DESIGN: The effect of...

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Autores principales: Shin, Yoo Seob, Shin, Hyang Ae, Kang, Sung Un, Kim, Jang Hee, Oh, Young-Taek, Park, Keun Hyung, Kim, Chul-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715464/
https://www.ncbi.nlm.nih.gov/pubmed/23874895
http://dx.doi.org/10.1371/journal.pone.0069151
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author Shin, Yoo Seob
Shin, Hyang Ae
Kang, Sung Un
Kim, Jang Hee
Oh, Young-Taek
Park, Keun Hyung
Kim, Chul-Ho
author_facet Shin, Yoo Seob
Shin, Hyang Ae
Kang, Sung Un
Kim, Jang Hee
Oh, Young-Taek
Park, Keun Hyung
Kim, Chul-Ho
author_sort Shin, Yoo Seob
collection PubMed
description PURPOSE: Radiation-induced oral mucositis limits the delivery of high-dose radiation to head and neck cancer. This study investigated the effectiveness of epicatechin (EC), a component of green tea extracts, on radiation-induced oral mucositis in vitro and in vivo. EXPERIMENTAL DESIGN: The effect of EC on radiation-induced cytotoxicity was analyzed in the human keratinocyte line HaCaT. Radiation-induced apoptosis, change in mitochondrial membrane potential (MMP), reactive oxygen species (ROS) generation and changes in the signaling pathway were investigated. In vivo therapeutic effects of EC for oral mucositis were explored in a rat model. Rats were monitored by daily inspections of the oral cavity, amount of oral intake, weight change and survival rate. For histopathologic evaluation, hematoxylin-eosin staining and TUNEL staining were performed. RESULTS: EC significantly inhibited radiation-induced apoptosis, change of MMP, and intracellular ROS generation in HaCaT cells. EC treatment markedly attenuated the expression of p-JNK, p-38, and cleaved caspase-3 after irradiation in the HaCaT cells. Rats with radiation-induced oral mucositis showed decreased oral intake, weight and survival rate, but oral administration of EC significantly restored all three parameters. Histopathologic changes were significantly decreased in the EC-treated irradiated rats. TUNEL staining of rat oral mucosa revealed that EC treatment significantly decreased radiation-induced apoptotic cells. CONCLUSIONS: This study suggests that EC significantly inhibited radiation-induced apoptosis in keratinocytes and rat oral mucosa and may be a safe and effective candidate treatment for the prevention of radiation-induced mucositis.
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spelling pubmed-37154642013-07-19 Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study Shin, Yoo Seob Shin, Hyang Ae Kang, Sung Un Kim, Jang Hee Oh, Young-Taek Park, Keun Hyung Kim, Chul-Ho PLoS One Research Article PURPOSE: Radiation-induced oral mucositis limits the delivery of high-dose radiation to head and neck cancer. This study investigated the effectiveness of epicatechin (EC), a component of green tea extracts, on radiation-induced oral mucositis in vitro and in vivo. EXPERIMENTAL DESIGN: The effect of EC on radiation-induced cytotoxicity was analyzed in the human keratinocyte line HaCaT. Radiation-induced apoptosis, change in mitochondrial membrane potential (MMP), reactive oxygen species (ROS) generation and changes in the signaling pathway were investigated. In vivo therapeutic effects of EC for oral mucositis were explored in a rat model. Rats were monitored by daily inspections of the oral cavity, amount of oral intake, weight change and survival rate. For histopathologic evaluation, hematoxylin-eosin staining and TUNEL staining were performed. RESULTS: EC significantly inhibited radiation-induced apoptosis, change of MMP, and intracellular ROS generation in HaCaT cells. EC treatment markedly attenuated the expression of p-JNK, p-38, and cleaved caspase-3 after irradiation in the HaCaT cells. Rats with radiation-induced oral mucositis showed decreased oral intake, weight and survival rate, but oral administration of EC significantly restored all three parameters. Histopathologic changes were significantly decreased in the EC-treated irradiated rats. TUNEL staining of rat oral mucosa revealed that EC treatment significantly decreased radiation-induced apoptotic cells. CONCLUSIONS: This study suggests that EC significantly inhibited radiation-induced apoptosis in keratinocytes and rat oral mucosa and may be a safe and effective candidate treatment for the prevention of radiation-induced mucositis. Public Library of Science 2013-07-18 /pmc/articles/PMC3715464/ /pubmed/23874895 http://dx.doi.org/10.1371/journal.pone.0069151 Text en © 2013 Shin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shin, Yoo Seob
Shin, Hyang Ae
Kang, Sung Un
Kim, Jang Hee
Oh, Young-Taek
Park, Keun Hyung
Kim, Chul-Ho
Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study
title Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study
title_full Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study
title_fullStr Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study
title_full_unstemmed Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study
title_short Effect of Epicatechin against Radiation-Induced Oral Mucositis: In Vitro and In Vivo Study
title_sort effect of epicatechin against radiation-induced oral mucositis: in vitro and in vivo study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715464/
https://www.ncbi.nlm.nih.gov/pubmed/23874895
http://dx.doi.org/10.1371/journal.pone.0069151
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