Cargando…

The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model

BACKGROUND/AIMS: DA-6034 has anti-inflammatory activities and exhibits cytoprotective effects in acute gastric injury models. However, explanations for the protective effects of DA-6034 on intestinal permeability are limited. This study sought to investigate the effect of DA-6034 on intestinal perme...

Descripción completa

Detalles Bibliográficos
Autores principales: Kwak, Dong Shin, Lee, Oh Young, Lee, Kang Nyeong, Jun, Dae Won, Lee, Hang Lak, Yoon, Byung Chul, Choi, Ho Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of Gut and Liver 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849694/
https://www.ncbi.nlm.nih.gov/pubmed/27114435
http://dx.doi.org/10.5009/gnl15251
_version_ 1782429580381913088
author Kwak, Dong Shin
Lee, Oh Young
Lee, Kang Nyeong
Jun, Dae Won
Lee, Hang Lak
Yoon, Byung Chul
Choi, Ho Soon
author_facet Kwak, Dong Shin
Lee, Oh Young
Lee, Kang Nyeong
Jun, Dae Won
Lee, Hang Lak
Yoon, Byung Chul
Choi, Ho Soon
author_sort Kwak, Dong Shin
collection PubMed
description BACKGROUND/AIMS: DA-6034 has anti-inflammatory activities and exhibits cytoprotective effects in acute gastric injury models. However, explanations for the protective effects of DA-6034 on intestinal permeability are limited. This study sought to investigate the effect of DA-6034 on intestinal permeability in an indomethacin-induced small intestinal injury model and its protective effect against small intestinal injury. METHODS: Rats in the treatment group received DA-6034 from days 0 to 2 and indomethacin from days 1 to 2. Rats in the control group received indomethacin from days 1 to 2. On the fourth day, the small intestines were examined to compare the severity of inflammation. Intestinal permeability was evaluated by using fluorescein isothiocyanate-labeled dextran. Western blotting was performed to confirm the association between DA-6034 and the extracellular signal-regulated kinase (ERK) pathway. RESULTS: The inflammation scores in the treatment group were lower than those in the control group, but the difference was statistically insignificant. Hemorrhagic lesions in the treatment group were broader than those in the control group, but the difference was statistically insignificant. Intestinal permeability was lower in the treatment group than in the control group. DA-6034 enhanced extracellular signal-regulated kinase expression, and intestinal permeability was negatively correlated with ERK expression. CONCLUSIONS: DA-6034 may decrease intestinal permeability in an indomethacin-induced intestinal injury model via the ERK pathway.
format Online
Article
Text
id pubmed-4849694
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Editorial Office of Gut and Liver
record_format MEDLINE/PubMed
spelling pubmed-48496942016-05-04 The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model Kwak, Dong Shin Lee, Oh Young Lee, Kang Nyeong Jun, Dae Won Lee, Hang Lak Yoon, Byung Chul Choi, Ho Soon Gut Liver Original Article BACKGROUND/AIMS: DA-6034 has anti-inflammatory activities and exhibits cytoprotective effects in acute gastric injury models. However, explanations for the protective effects of DA-6034 on intestinal permeability are limited. This study sought to investigate the effect of DA-6034 on intestinal permeability in an indomethacin-induced small intestinal injury model and its protective effect against small intestinal injury. METHODS: Rats in the treatment group received DA-6034 from days 0 to 2 and indomethacin from days 1 to 2. Rats in the control group received indomethacin from days 1 to 2. On the fourth day, the small intestines were examined to compare the severity of inflammation. Intestinal permeability was evaluated by using fluorescein isothiocyanate-labeled dextran. Western blotting was performed to confirm the association between DA-6034 and the extracellular signal-regulated kinase (ERK) pathway. RESULTS: The inflammation scores in the treatment group were lower than those in the control group, but the difference was statistically insignificant. Hemorrhagic lesions in the treatment group were broader than those in the control group, but the difference was statistically insignificant. Intestinal permeability was lower in the treatment group than in the control group. DA-6034 enhanced extracellular signal-regulated kinase expression, and intestinal permeability was negatively correlated with ERK expression. CONCLUSIONS: DA-6034 may decrease intestinal permeability in an indomethacin-induced intestinal injury model via the ERK pathway. Editorial Office of Gut and Liver 2016-05 2016-05-15 /pmc/articles/PMC4849694/ /pubmed/27114435 http://dx.doi.org/10.5009/gnl15251 Text en Copyright © 2016 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kwak, Dong Shin
Lee, Oh Young
Lee, Kang Nyeong
Jun, Dae Won
Lee, Hang Lak
Yoon, Byung Chul
Choi, Ho Soon
The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model
title The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model
title_full The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model
title_fullStr The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model
title_full_unstemmed The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model
title_short The Effect of DA-6034 on Intestinal Permeability in an Indomethacin-Induced Small Intestinal Injury Model
title_sort effect of da-6034 on intestinal permeability in an indomethacin-induced small intestinal injury model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849694/
https://www.ncbi.nlm.nih.gov/pubmed/27114435
http://dx.doi.org/10.5009/gnl15251
work_keys_str_mv AT kwakdongshin theeffectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT leeohyoung theeffectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT leekangnyeong theeffectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT jundaewon theeffectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT leehanglak theeffectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT yoonbyungchul theeffectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT choihosoon theeffectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT kwakdongshin effectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT leeohyoung effectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT leekangnyeong effectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT jundaewon effectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT leehanglak effectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT yoonbyungchul effectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel
AT choihosoon effectofda6034onintestinalpermeabilityinanindomethacininducedsmallintestinalinjurymodel