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The effects of acacia honey on in vitro corneal abrasion wound healing model

BACKGROUND: Acacia honey (AH) has been proven to improve skin wound healing, but its therapeutic effects on corneal epithelium has not been elucidated to date. This study aimed to investigate the effects of AH on cultured corneal epithelial cells (CEC) on in vitro corneal abrasion wound healing mode...

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Autores principales: Ker-Woon, Choy, Abd Ghafar, Norzana, Kien Hui, Chua, Mohd Yusof, Yasmin Anum, Wan Ngah, Wan Zurinah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340287/
https://www.ncbi.nlm.nih.gov/pubmed/25887200
http://dx.doi.org/10.1186/s12860-015-0053-9
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author Ker-Woon, Choy
Abd Ghafar, Norzana
Kien Hui, Chua
Mohd Yusof, Yasmin Anum
Wan Ngah, Wan Zurinah
author_facet Ker-Woon, Choy
Abd Ghafar, Norzana
Kien Hui, Chua
Mohd Yusof, Yasmin Anum
Wan Ngah, Wan Zurinah
author_sort Ker-Woon, Choy
collection PubMed
description BACKGROUND: Acacia honey (AH) has been proven to improve skin wound healing, but its therapeutic effects on corneal epithelium has not been elucidated to date. This study aimed to investigate the effects of AH on cultured corneal epithelial cells (CEC) on in vitro corneal abrasion wound healing model. Six New Zealand white rabbits’ CEC were isolated and cultured until passage 1. Circular wound area was created onto a confluent monolayer CEC using a corneal trephine which mimicked corneal abrasion and treated with 0.025% AH supplemented in basal medium (BM) and complete cornea medium (CCM). Wound healing was measured as the percentage of wound closure by the migration of CEC on day 0, day 3 and day 6, post wound creation. The morphological changes of CEC were assessed via phase contrast microscopy. Gene and protein expressions of cytokeratin (CK3), fibronectin and cluster of differentiation 44 (CD44) in AH treated groups and control groups were determined by real-time PCR and immunocytochemistry, respectively. RESULTS: Cultured CEC exhibited similar morphology of polygonal shaped cells in all culture media. CEC cultured in AH-supplemented media showed higher percentage of wound closure compared to the controls. Gene expression of CK3 increased in AH-supplemented groups throughout the study. Fibronectin expression was increased at the initial stage while CD44 expression was increased at day 3, post wound creation. The protein expression of CEC cultured in all media was in accordance to their respective gene expressions. CONCLUSION: Supplementation of AH in BM and CCM media accelerates CEC wound closure of the in vitro corneal abrasion model by increasing the expression of genes and proteins associated with CEC wound healing.
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spelling pubmed-43402872015-02-26 The effects of acacia honey on in vitro corneal abrasion wound healing model Ker-Woon, Choy Abd Ghafar, Norzana Kien Hui, Chua Mohd Yusof, Yasmin Anum Wan Ngah, Wan Zurinah BMC Cell Biol Research Article BACKGROUND: Acacia honey (AH) has been proven to improve skin wound healing, but its therapeutic effects on corneal epithelium has not been elucidated to date. This study aimed to investigate the effects of AH on cultured corneal epithelial cells (CEC) on in vitro corneal abrasion wound healing model. Six New Zealand white rabbits’ CEC were isolated and cultured until passage 1. Circular wound area was created onto a confluent monolayer CEC using a corneal trephine which mimicked corneal abrasion and treated with 0.025% AH supplemented in basal medium (BM) and complete cornea medium (CCM). Wound healing was measured as the percentage of wound closure by the migration of CEC on day 0, day 3 and day 6, post wound creation. The morphological changes of CEC were assessed via phase contrast microscopy. Gene and protein expressions of cytokeratin (CK3), fibronectin and cluster of differentiation 44 (CD44) in AH treated groups and control groups were determined by real-time PCR and immunocytochemistry, respectively. RESULTS: Cultured CEC exhibited similar morphology of polygonal shaped cells in all culture media. CEC cultured in AH-supplemented media showed higher percentage of wound closure compared to the controls. Gene expression of CK3 increased in AH-supplemented groups throughout the study. Fibronectin expression was increased at the initial stage while CD44 expression was increased at day 3, post wound creation. The protein expression of CEC cultured in all media was in accordance to their respective gene expressions. CONCLUSION: Supplementation of AH in BM and CCM media accelerates CEC wound closure of the in vitro corneal abrasion model by increasing the expression of genes and proteins associated with CEC wound healing. BioMed Central 2015-02-18 /pmc/articles/PMC4340287/ /pubmed/25887200 http://dx.doi.org/10.1186/s12860-015-0053-9 Text en © Ker-Woon et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ker-Woon, Choy
Abd Ghafar, Norzana
Kien Hui, Chua
Mohd Yusof, Yasmin Anum
Wan Ngah, Wan Zurinah
The effects of acacia honey on in vitro corneal abrasion wound healing model
title The effects of acacia honey on in vitro corneal abrasion wound healing model
title_full The effects of acacia honey on in vitro corneal abrasion wound healing model
title_fullStr The effects of acacia honey on in vitro corneal abrasion wound healing model
title_full_unstemmed The effects of acacia honey on in vitro corneal abrasion wound healing model
title_short The effects of acacia honey on in vitro corneal abrasion wound healing model
title_sort effects of acacia honey on in vitro corneal abrasion wound healing model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340287/
https://www.ncbi.nlm.nih.gov/pubmed/25887200
http://dx.doi.org/10.1186/s12860-015-0053-9
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