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Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats

A correlation between endoplasmic reticulum (ER) stress and laxative effects was first reported in a constipation model treated with an aqueous extract of Liriope platyphylla (AEtLP) roots. To investigate the correlation between the laxative effect of uridine (Urd) and ER stress response, alteration...

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Autores principales: Kim, Ji Eun, Song, Bo Ram, Yun, Woo Bin, Choi, Jun Young, Park, Jin Ju, Lee, Mi Rim, Hwang, Dae Youn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for Laboratory Animal Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792531/
https://www.ncbi.nlm.nih.gov/pubmed/29399027
http://dx.doi.org/10.5625/lar.2017.33.4.298
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author Kim, Ji Eun
Song, Bo Ram
Yun, Woo Bin
Choi, Jun Young
Park, Jin Ju
Lee, Mi Rim
Hwang, Dae Youn
author_facet Kim, Ji Eun
Song, Bo Ram
Yun, Woo Bin
Choi, Jun Young
Park, Jin Ju
Lee, Mi Rim
Hwang, Dae Youn
author_sort Kim, Ji Eun
collection PubMed
description A correlation between endoplasmic reticulum (ER) stress and laxative effects was first reported in a constipation model treated with an aqueous extract of Liriope platyphylla (AEtLP) roots. To investigate the correlation between the laxative effect of uridine (Urd) and ER stress response, alterations in the key parameters for ER stress were measured in loperamide (Lop) induced constipation Sprague Dawley (SD) rats treated with Urd. The efficacy of the laxative effect of Urd was notable on the symptoms of chronic constipation, including alteration of stool parameters and structure of the transverse colon, in Lop induced constipated SD rats. In the PERK/eIF2-ATF4 pathway of ER stress response, the levels of eukaryotic initiation factor 2 alpha (eIF2α) phosphorylation and DNA damage-inducible protein (GADD34) transcripts were significantly enhanced in the Lop+Vehicle treated group. However, the levels were restored in the Lop+Urd treated group, although few differences were detected in the decrease rate. Similar changes were observed for levels of inositol-requiring enzyme 1 beta (IRE1β) phosphorylation and X-box binding protein 1 (XBP-1) transcript in the IRE1α/XBP pathway. Furthermore, the number of ER stress-induced apoptotic cells and Bax and Bcl-2 expression were recovered in the Lop+Urd treated group compared to the Lop+Vehicle treated group. The results of the present study therefore provide first evidence that the laxative effects of Urd may be tightly correlated with the recovery of ER stress response in constipation models.
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spelling pubmed-57925312018-02-02 Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats Kim, Ji Eun Song, Bo Ram Yun, Woo Bin Choi, Jun Young Park, Jin Ju Lee, Mi Rim Hwang, Dae Youn Lab Anim Res Original Article A correlation between endoplasmic reticulum (ER) stress and laxative effects was first reported in a constipation model treated with an aqueous extract of Liriope platyphylla (AEtLP) roots. To investigate the correlation between the laxative effect of uridine (Urd) and ER stress response, alterations in the key parameters for ER stress were measured in loperamide (Lop) induced constipation Sprague Dawley (SD) rats treated with Urd. The efficacy of the laxative effect of Urd was notable on the symptoms of chronic constipation, including alteration of stool parameters and structure of the transverse colon, in Lop induced constipated SD rats. In the PERK/eIF2-ATF4 pathway of ER stress response, the levels of eukaryotic initiation factor 2 alpha (eIF2α) phosphorylation and DNA damage-inducible protein (GADD34) transcripts were significantly enhanced in the Lop+Vehicle treated group. However, the levels were restored in the Lop+Urd treated group, although few differences were detected in the decrease rate. Similar changes were observed for levels of inositol-requiring enzyme 1 beta (IRE1β) phosphorylation and X-box binding protein 1 (XBP-1) transcript in the IRE1α/XBP pathway. Furthermore, the number of ER stress-induced apoptotic cells and Bax and Bcl-2 expression were recovered in the Lop+Urd treated group compared to the Lop+Vehicle treated group. The results of the present study therefore provide first evidence that the laxative effects of Urd may be tightly correlated with the recovery of ER stress response in constipation models. Korean Association for Laboratory Animal Science 2017-12 2017-12-31 /pmc/articles/PMC5792531/ /pubmed/29399027 http://dx.doi.org/10.5625/lar.2017.33.4.298 Text en Copyright © 2017 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Ji Eun
Song, Bo Ram
Yun, Woo Bin
Choi, Jun Young
Park, Jin Ju
Lee, Mi Rim
Hwang, Dae Youn
Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats
title Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats
title_full Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats
title_fullStr Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats
title_full_unstemmed Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats
title_short Correlation between laxative effects of uridine and suppression of ER stress in loperamide induced constipated SD rats
title_sort correlation between laxative effects of uridine and suppression of er stress in loperamide induced constipated sd rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792531/
https://www.ncbi.nlm.nih.gov/pubmed/29399027
http://dx.doi.org/10.5625/lar.2017.33.4.298
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