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Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study
Oral submucous fibrosis (OSF) is a potentially malignant disorder that is characterized by a progressive fibrosis in the oral submucosa. Arecoline, an alkaloid compound of the areca nut, is reported to be a major aetiological factor in the development of OSF. Low-power laser irradiation (LPLI) has b...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379159/ https://www.ncbi.nlm.nih.gov/pubmed/28233766 http://dx.doi.org/10.1038/ijos.2016.49 |
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author | Yeh, Mei-Chun Chen, Ker-Kong Chiang, Min-Hsuan Chen, Chia-Hsin Chen, Ping-Ho Lee, Huey-Er Wang, Yan-Hsiung |
author_facet | Yeh, Mei-Chun Chen, Ker-Kong Chiang, Min-Hsuan Chen, Chia-Hsin Chen, Ping-Ho Lee, Huey-Er Wang, Yan-Hsiung |
author_sort | Yeh, Mei-Chun |
collection | PubMed |
description | Oral submucous fibrosis (OSF) is a potentially malignant disorder that is characterized by a progressive fibrosis in the oral submucosa. Arecoline, an alkaloid compound of the areca nut, is reported to be a major aetiological factor in the development of OSF. Low-power laser irradiation (LPLI) has been reported to be beneficial in fibrosis prevention in different damaged organs. The aim of this study was to investigate the potential therapeutic effects of LPLI on arecoline-induced fibrosis. Arecoline-stimulated human gingival fibroblasts (HGFs) were treated with or without LPLI. The expression levels of the fibrotic marker genes alpha-smooth muscle actin (α-SMA) and connective tissue growth factor (CTGF/CCN2) were analysed by quantitative real-time reverse transcription polymerase chain reaction (RT-PCR) and western blots. In addition, the transcriptional activity of CCN2 was further determined by a reporter assay. The results indicated that arecoline increased the messenger RNA and protein expression of CCN2 and α-SMA in HGF. Interestingly, both LPLI and forskolin, an adenylyl cyclase activator, reduced the expression of arecoline-mediated fibrotic marker genes and inhibited the transcriptional activity of CCN2. Moreover, pretreatment with SQ22536, an adenylyl cyclase inhibitor, blocked LPLI's inhibition of the expression of arecoline-mediated fibrotic marker genes. Our data suggest that LPLI may inhibit the expression of arecoline-mediated fibrotic marker genes via the cAMP signalling pathway. |
format | Online Article Text |
id | pubmed-5379159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53791592017-04-17 Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study Yeh, Mei-Chun Chen, Ker-Kong Chiang, Min-Hsuan Chen, Chia-Hsin Chen, Ping-Ho Lee, Huey-Er Wang, Yan-Hsiung Int J Oral Sci Original Article Oral submucous fibrosis (OSF) is a potentially malignant disorder that is characterized by a progressive fibrosis in the oral submucosa. Arecoline, an alkaloid compound of the areca nut, is reported to be a major aetiological factor in the development of OSF. Low-power laser irradiation (LPLI) has been reported to be beneficial in fibrosis prevention in different damaged organs. The aim of this study was to investigate the potential therapeutic effects of LPLI on arecoline-induced fibrosis. Arecoline-stimulated human gingival fibroblasts (HGFs) were treated with or without LPLI. The expression levels of the fibrotic marker genes alpha-smooth muscle actin (α-SMA) and connective tissue growth factor (CTGF/CCN2) were analysed by quantitative real-time reverse transcription polymerase chain reaction (RT-PCR) and western blots. In addition, the transcriptional activity of CCN2 was further determined by a reporter assay. The results indicated that arecoline increased the messenger RNA and protein expression of CCN2 and α-SMA in HGF. Interestingly, both LPLI and forskolin, an adenylyl cyclase activator, reduced the expression of arecoline-mediated fibrotic marker genes and inhibited the transcriptional activity of CCN2. Moreover, pretreatment with SQ22536, an adenylyl cyclase inhibitor, blocked LPLI's inhibition of the expression of arecoline-mediated fibrotic marker genes. Our data suggest that LPLI may inhibit the expression of arecoline-mediated fibrotic marker genes via the cAMP signalling pathway. Nature Publishing Group 2017-03 2017-02-24 /pmc/articles/PMC5379159/ /pubmed/28233766 http://dx.doi.org/10.1038/ijos.2016.49 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Original Article Yeh, Mei-Chun Chen, Ker-Kong Chiang, Min-Hsuan Chen, Chia-Hsin Chen, Ping-Ho Lee, Huey-Er Wang, Yan-Hsiung Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study |
title | Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study |
title_full | Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study |
title_fullStr | Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study |
title_full_unstemmed | Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study |
title_short | Low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study |
title_sort | low-power laser irradiation inhibits arecoline-induced fibrosis: an in vitro study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379159/ https://www.ncbi.nlm.nih.gov/pubmed/28233766 http://dx.doi.org/10.1038/ijos.2016.49 |
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