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Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function

Nasolacrimal duct obstruction (NLDO) is thought to be due to inflammation and fibrosis of lacrimal duct epithelial cells (LDECs). Here we investigated the effect of rebamipide, a drug that is used for the protection of the mucosa and the treatment of gastritis and gastroduodenal ulcers, on LDECs, bo...

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Autores principales: Tanaka, Hiroshi, Nakayama, Tomomichi, Tsukamoto, Michiko, Watanabe, Akihide, Nakamura, Takahiro, Yokoi, Norihiko, Sotozono, Chie, Kinoshita, Shigeru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997454/
https://www.ncbi.nlm.nih.gov/pubmed/32015381
http://dx.doi.org/10.1038/s41598-020-58314-x
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author Tanaka, Hiroshi
Nakayama, Tomomichi
Tsukamoto, Michiko
Watanabe, Akihide
Nakamura, Takahiro
Yokoi, Norihiko
Sotozono, Chie
Kinoshita, Shigeru
author_facet Tanaka, Hiroshi
Nakayama, Tomomichi
Tsukamoto, Michiko
Watanabe, Akihide
Nakamura, Takahiro
Yokoi, Norihiko
Sotozono, Chie
Kinoshita, Shigeru
author_sort Tanaka, Hiroshi
collection PubMed
description Nasolacrimal duct obstruction (NLDO) is thought to be due to inflammation and fibrosis of lacrimal duct epithelial cells (LDECs). Here we investigated the effect of rebamipide, a drug that is used for the protection of the mucosa and the treatment of gastritis and gastroduodenal ulcers, on LDECs, both in vitro and in vivo. In this study, LDECs were cultured from rabbit lacrimal duct tissues, and the barrier function of LEDCs was examined in vitro via transepithelial electrical resistance (TER) measurement, with or without interleukin (IL)-6 and/or rebamipide. For the in vivo examination, benzalkonium chloride (BAC) was injected into the rabbit lacrimal ducts, followed by the application of rebamipide or a placebo vehicle alone. The results of the in vitro examination revealed a significant decrease in TER in the group treated with IL-6 alone compared with the placebo-vehicle group (p < 0.05) and the group treated with IL-6 and rebamipide (p < 0.01). The results of the in vivo examination revealed that the infiltration of neutrophils under the basement membrane and the disruption of tight junction proteins with BAC injection and rebamipide attenuates the disturbance of tissue construction. These results suggest that rebamipide protects LDECs via an anti-inflammatory effect and preserves the barrier function of those cells.
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spelling pubmed-69974542020-02-10 Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function Tanaka, Hiroshi Nakayama, Tomomichi Tsukamoto, Michiko Watanabe, Akihide Nakamura, Takahiro Yokoi, Norihiko Sotozono, Chie Kinoshita, Shigeru Sci Rep Article Nasolacrimal duct obstruction (NLDO) is thought to be due to inflammation and fibrosis of lacrimal duct epithelial cells (LDECs). Here we investigated the effect of rebamipide, a drug that is used for the protection of the mucosa and the treatment of gastritis and gastroduodenal ulcers, on LDECs, both in vitro and in vivo. In this study, LDECs were cultured from rabbit lacrimal duct tissues, and the barrier function of LEDCs was examined in vitro via transepithelial electrical resistance (TER) measurement, with or without interleukin (IL)-6 and/or rebamipide. For the in vivo examination, benzalkonium chloride (BAC) was injected into the rabbit lacrimal ducts, followed by the application of rebamipide or a placebo vehicle alone. The results of the in vitro examination revealed a significant decrease in TER in the group treated with IL-6 alone compared with the placebo-vehicle group (p < 0.05) and the group treated with IL-6 and rebamipide (p < 0.01). The results of the in vivo examination revealed that the infiltration of neutrophils under the basement membrane and the disruption of tight junction proteins with BAC injection and rebamipide attenuates the disturbance of tissue construction. These results suggest that rebamipide protects LDECs via an anti-inflammatory effect and preserves the barrier function of those cells. Nature Publishing Group UK 2020-02-03 /pmc/articles/PMC6997454/ /pubmed/32015381 http://dx.doi.org/10.1038/s41598-020-58314-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tanaka, Hiroshi
Nakayama, Tomomichi
Tsukamoto, Michiko
Watanabe, Akihide
Nakamura, Takahiro
Yokoi, Norihiko
Sotozono, Chie
Kinoshita, Shigeru
Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function
title Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function
title_full Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function
title_fullStr Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function
title_full_unstemmed Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function
title_short Rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function
title_sort rebamipide promotes lacrimal duct epithelial cell survival via protecting barrier function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997454/
https://www.ncbi.nlm.nih.gov/pubmed/32015381
http://dx.doi.org/10.1038/s41598-020-58314-x
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