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Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole
Postoperative ileus (POI), a symptom that occurs after abdominal surgery, reduces gastrointestinal motility. Although its mechanism is unclear, POI symptoms are known to be caused by inflammation 6 to 72 h after surgery. As proton pump inhibitors exhibit protective effect against acute inflammation,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Physiological Society and The Korean Society of Pharmacology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552821/ https://www.ncbi.nlm.nih.gov/pubmed/34697261 http://dx.doi.org/10.4196/kjpp.2021.25.6.507 |
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author | Kim, Geon Min Sohn, Hee Ju Choi, Won Seok Sohn, Uy Dong |
author_facet | Kim, Geon Min Sohn, Hee Ju Choi, Won Seok Sohn, Uy Dong |
author_sort | Kim, Geon Min |
collection | PubMed |
description | Postoperative ileus (POI), a symptom that occurs after abdominal surgery, reduces gastrointestinal motility. Although its mechanism is unclear, POI symptoms are known to be caused by inflammation 6 to 72 h after surgery. As proton pump inhibitors exhibit protective effect against acute inflammation, the purpose of this study was to determine the effect of ilaprazole on a POI rat model. POI was induced in rats by abdominal surgery. Rats were divided into six groups: control: normal rat + 0.5% CMC-Na, vehicle: POI rat + 0.5% CMC-Na, mosapride: POI rat + mosapride 2 mg/kg, ilaprazole 1 mg/kg: POI rat + ilaprazole 1 mg/kg, ilaprazole 3 mg/kg: POI rat + ilaprazole 3 mg/kg, and ilaprazole 10 mg/kg: POI rat + ilaprazole 10 mg/kg. Gastrointestinal motility was confirmed by measuring gastric emptying (GE) and gastrointestinal transit (GIT). In the small intestine, inflammation was confirmed by measuring TNF-α and IL-1β; oxidative stress was confirmed by SOD, GSH, and MDA levels; and histological changes were observed by H&E staining. Based on the findings, GE and GIT were decreased in the vehicle group and improved in the ilaprazole 10 mg/kg group. In the ilaprazole 10 mg/kg group, TNF-α and IL-1β levels were decreased, SOD and GSH levels were increased, and MDA levels were decreased. Histological damage was also reduced in the ilaprazole-treated groups. These findings suggest that ilaprazole prevents the decrease in gastrointestinal motility, a major symptom of postoperative ileus, and reduces inflammation and oxidative stress. |
format | Online Article Text |
id | pubmed-8552821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Korean Physiological Society and The Korean Society of Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-85528212021-11-10 Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole Kim, Geon Min Sohn, Hee Ju Choi, Won Seok Sohn, Uy Dong Korean J Physiol Pharmacol Original Article Postoperative ileus (POI), a symptom that occurs after abdominal surgery, reduces gastrointestinal motility. Although its mechanism is unclear, POI symptoms are known to be caused by inflammation 6 to 72 h after surgery. As proton pump inhibitors exhibit protective effect against acute inflammation, the purpose of this study was to determine the effect of ilaprazole on a POI rat model. POI was induced in rats by abdominal surgery. Rats were divided into six groups: control: normal rat + 0.5% CMC-Na, vehicle: POI rat + 0.5% CMC-Na, mosapride: POI rat + mosapride 2 mg/kg, ilaprazole 1 mg/kg: POI rat + ilaprazole 1 mg/kg, ilaprazole 3 mg/kg: POI rat + ilaprazole 3 mg/kg, and ilaprazole 10 mg/kg: POI rat + ilaprazole 10 mg/kg. Gastrointestinal motility was confirmed by measuring gastric emptying (GE) and gastrointestinal transit (GIT). In the small intestine, inflammation was confirmed by measuring TNF-α and IL-1β; oxidative stress was confirmed by SOD, GSH, and MDA levels; and histological changes were observed by H&E staining. Based on the findings, GE and GIT were decreased in the vehicle group and improved in the ilaprazole 10 mg/kg group. In the ilaprazole 10 mg/kg group, TNF-α and IL-1β levels were decreased, SOD and GSH levels were increased, and MDA levels were decreased. Histological damage was also reduced in the ilaprazole-treated groups. These findings suggest that ilaprazole prevents the decrease in gastrointestinal motility, a major symptom of postoperative ileus, and reduces inflammation and oxidative stress. The Korean Physiological Society and The Korean Society of Pharmacology 2021-11-01 2021-11-01 /pmc/articles/PMC8552821/ /pubmed/34697261 http://dx.doi.org/10.4196/kjpp.2021.25.6.507 Text en Copyright © Korean J Physiol Pharmacol https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://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 Kim, Geon Min Sohn, Hee Ju Choi, Won Seok Sohn, Uy Dong Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole |
title | Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole |
title_full | Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole |
title_fullStr | Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole |
title_full_unstemmed | Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole |
title_short | Improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole |
title_sort | improved motility in the gastrointestinal tract of a postoperative ileus rat model with ilaprazole |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552821/ https://www.ncbi.nlm.nih.gov/pubmed/34697261 http://dx.doi.org/10.4196/kjpp.2021.25.6.507 |
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