Effect of epicatechin against radiation-induced oral mucositis: in vitro and in vivo study

PLoS One. 2013 Jul 18;8(7):e69151. doi: 10.1371/journal.pone.0069151. Print 2013.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Apoptosis / drug effects
  • Blotting, Western
  • Catechin / pharmacology*
  • Catechin / therapeutic use
  • Female
  • Fluorescein-5-isothiocyanate
  • Head and Neck Neoplasms / radiotherapy*
  • Humans
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Keratinocytes / drug effects
  • Membrane Potential, Mitochondrial / drug effects
  • Microscopy, Fluorescence
  • Propidium
  • Radiotherapy / adverse effects*
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects
  • Stomatitis / drug therapy*
  • Stomatitis / etiology*

Substances

  • Reactive Oxygen Species
  • Propidium
  • Catechin
  • Fluorescein-5-isothiocyanate

Grants and funding

This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (2010-0012821) and CCRB through the “GRRC” Project of Gyeonggi Provincial Government, Korea (GRRC Ajou-2012-A03). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.