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Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model

Introduction. Short bowel syndrome can crop up if more than 50% of small intestine is resected or when less than 100 cm of small bowel is left. Glutamine is the main food source of enterocytes. Curcumin has protective effects on intestinal ischemia-reperfusion damage. Nesfatin-1 is a satiety molecul...

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Autores principales: Gulcicek, Osman Bilgin, Solmaz, Ali, Yiğitbaş, Hakan, Ercetin, Candas, Yavuz, Erkan, Ozdogan, Kamil, Arici, Sinan, Akkalp, Asli Kahraman, Sarac, Tulin, Çelebi, Fatih, Celik, Atilla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972927/
https://www.ncbi.nlm.nih.gov/pubmed/27525002
http://dx.doi.org/10.1155/2016/2081962
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author Gulcicek, Osman Bilgin
Solmaz, Ali
Yiğitbaş, Hakan
Ercetin, Candas
Yavuz, Erkan
Ozdogan, Kamil
Arici, Sinan
Akkalp, Asli Kahraman
Sarac, Tulin
Çelebi, Fatih
Celik, Atilla
author_facet Gulcicek, Osman Bilgin
Solmaz, Ali
Yiğitbaş, Hakan
Ercetin, Candas
Yavuz, Erkan
Ozdogan, Kamil
Arici, Sinan
Akkalp, Asli Kahraman
Sarac, Tulin
Çelebi, Fatih
Celik, Atilla
author_sort Gulcicek, Osman Bilgin
collection PubMed
description Introduction. Short bowel syndrome can crop up if more than 50% of small intestine is resected or when less than 100 cm of small bowel is left. Glutamine is the main food source of enterocytes. Curcumin has protective effects on intestinal ischemia-reperfusion damage. Nesfatin-1 is a satiety molecule. It has protective effects on gastric mucosa. The primary purpose of this study is to compare effects of glutamine, curcumin, and nesfatin-1 on the gastric serosal surface neomucosa formation on rats. Materials and Methods. 24 Wistar-Hannover rats were randomly divided into 4 groups and treated with saline, glutamine, curcumin, and nesfatin-1 after ileogastric anastomosis. After 14 days all rats were euthanized, and blood was collected. En bloc resection of anastomotic part was performed for histopathological examination. Results. PDGF, TGF-β, and VEGF levels and neomucosa formation were higher in glutamine group (p = 0.003, p = 0.003, and p = 0.025). Glutamine promotes the intestinal neomucosa formation on the gastric serosal surface and augments growth factors essential for neomucosa formation on rats. Conclusion. Glutamine may be used in short bowel syndrome for increasing the absorption surface area. But that needs to be determined by adequately powered clinical trials.
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spelling pubmed-49729272016-08-14 Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model Gulcicek, Osman Bilgin Solmaz, Ali Yiğitbaş, Hakan Ercetin, Candas Yavuz, Erkan Ozdogan, Kamil Arici, Sinan Akkalp, Asli Kahraman Sarac, Tulin Çelebi, Fatih Celik, Atilla Gastroenterol Res Pract Research Article Introduction. Short bowel syndrome can crop up if more than 50% of small intestine is resected or when less than 100 cm of small bowel is left. Glutamine is the main food source of enterocytes. Curcumin has protective effects on intestinal ischemia-reperfusion damage. Nesfatin-1 is a satiety molecule. It has protective effects on gastric mucosa. The primary purpose of this study is to compare effects of glutamine, curcumin, and nesfatin-1 on the gastric serosal surface neomucosa formation on rats. Materials and Methods. 24 Wistar-Hannover rats were randomly divided into 4 groups and treated with saline, glutamine, curcumin, and nesfatin-1 after ileogastric anastomosis. After 14 days all rats were euthanized, and blood was collected. En bloc resection of anastomotic part was performed for histopathological examination. Results. PDGF, TGF-β, and VEGF levels and neomucosa formation were higher in glutamine group (p = 0.003, p = 0.003, and p = 0.025). Glutamine promotes the intestinal neomucosa formation on the gastric serosal surface and augments growth factors essential for neomucosa formation on rats. Conclusion. Glutamine may be used in short bowel syndrome for increasing the absorption surface area. But that needs to be determined by adequately powered clinical trials. Hindawi Publishing Corporation 2016 2016-07-21 /pmc/articles/PMC4972927/ /pubmed/27525002 http://dx.doi.org/10.1155/2016/2081962 Text en Copyright © 2016 Osman Bilgin Gulcicek et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gulcicek, Osman Bilgin
Solmaz, Ali
Yiğitbaş, Hakan
Ercetin, Candas
Yavuz, Erkan
Ozdogan, Kamil
Arici, Sinan
Akkalp, Asli Kahraman
Sarac, Tulin
Çelebi, Fatih
Celik, Atilla
Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model
title Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model
title_full Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model
title_fullStr Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model
title_full_unstemmed Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model
title_short Comparison of the Effects of Glutamine, Curcumin, and Nesfatin-1 on the Gastric Serosal Surface Neomucosa Formation: An Experimental Rodent Model
title_sort comparison of the effects of glutamine, curcumin, and nesfatin-1 on the gastric serosal surface neomucosa formation: an experimental rodent model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972927/
https://www.ncbi.nlm.nih.gov/pubmed/27525002
http://dx.doi.org/10.1155/2016/2081962
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