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Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model

INTRODUCTION: Mesenteric ischemia/reperfusion (I/R) injury is a serious clinical condition. There were a lot of experimental studies performed in the treatment of I/R injury. To our knowledge, this is the first experimental study with effects of sesamin on I/R injury model. We aimed to investigate t...

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Autores principales: Sayhan, Mustafa B., Oguz, Serhat, Salt, Ömer, Can, Nuray, Ozgurtas, Taner, Yalta, Tulın D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855156/
https://www.ncbi.nlm.nih.gov/pubmed/31749888
http://dx.doi.org/10.5114/aoms.2017.68535
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author Sayhan, Mustafa B.
Oguz, Serhat
Salt, Ömer
Can, Nuray
Ozgurtas, Taner
Yalta, Tulın D.
author_facet Sayhan, Mustafa B.
Oguz, Serhat
Salt, Ömer
Can, Nuray
Ozgurtas, Taner
Yalta, Tulın D.
author_sort Sayhan, Mustafa B.
collection PubMed
description INTRODUCTION: Mesenteric ischemia/reperfusion (I/R) injury is a serious clinical condition. There were a lot of experimental studies performed in the treatment of I/R injury. To our knowledge, this is the first experimental study with effects of sesamin on I/R injury model. We aimed to investigate the protective effect of sesamin on mesenteric I/R injury model. MATERIAL AND METHODS: A total of 32 male Sprague-Dawley rats were divided into four groups. Control group: superior mesenteric artery (SMA) exposed without clamping. I/R group: SMA was clamped for 60 min and then reperfused for 2 h. Sesamin group (S): 30 mg/kg sesamin were given for 5 days, and SMA exposed without clamping. I/R + S group: 30 mg/kg sesamin were given for 5 days, SMA was clamped for 60 min, and then reperfused for 2 h. Plasma and tissue oxidant parameters were investigated as well as histopathological evaluation. RESULTS: Plasma and tissue total antioxidant status (TAS) levels were significantly higher in I/R + S group compared to the rest (p < 0.005). The plasma TAS levels in I/R group was significantly low. The highest tissue TAS levels were detected in I/R + S group. The high levels of plasma and tissue TOS were found in I/R + S group. Plasma and tissue OSI levels were significantly higher in I/R group. Histopathologic evaluation showed that the mean level of intestinal tissue injury score in I/R group was 2.75 and 1.38 in I/R + S group. CONCLUSIONS: Sesamin helps to protect the intestinal tissue at the cellular level by reducing the oxidative stress and inflammation at both the plasma and tissue levels in the experimental I/R model.
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spelling pubmed-68551562019-11-20 Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model Sayhan, Mustafa B. Oguz, Serhat Salt, Ömer Can, Nuray Ozgurtas, Taner Yalta, Tulın D. Arch Med Sci Experimental Research INTRODUCTION: Mesenteric ischemia/reperfusion (I/R) injury is a serious clinical condition. There were a lot of experimental studies performed in the treatment of I/R injury. To our knowledge, this is the first experimental study with effects of sesamin on I/R injury model. We aimed to investigate the protective effect of sesamin on mesenteric I/R injury model. MATERIAL AND METHODS: A total of 32 male Sprague-Dawley rats were divided into four groups. Control group: superior mesenteric artery (SMA) exposed without clamping. I/R group: SMA was clamped for 60 min and then reperfused for 2 h. Sesamin group (S): 30 mg/kg sesamin were given for 5 days, and SMA exposed without clamping. I/R + S group: 30 mg/kg sesamin were given for 5 days, SMA was clamped for 60 min, and then reperfused for 2 h. Plasma and tissue oxidant parameters were investigated as well as histopathological evaluation. RESULTS: Plasma and tissue total antioxidant status (TAS) levels were significantly higher in I/R + S group compared to the rest (p < 0.005). The plasma TAS levels in I/R group was significantly low. The highest tissue TAS levels were detected in I/R + S group. The high levels of plasma and tissue TOS were found in I/R + S group. Plasma and tissue OSI levels were significantly higher in I/R group. Histopathologic evaluation showed that the mean level of intestinal tissue injury score in I/R group was 2.75 and 1.38 in I/R + S group. CONCLUSIONS: Sesamin helps to protect the intestinal tissue at the cellular level by reducing the oxidative stress and inflammation at both the plasma and tissue levels in the experimental I/R model. Termedia Publishing House 2018-12-10 2019-10 /pmc/articles/PMC6855156/ /pubmed/31749888 http://dx.doi.org/10.5114/aoms.2017.68535 Text en Copyright: © 2018 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Experimental Research
Sayhan, Mustafa B.
Oguz, Serhat
Salt, Ömer
Can, Nuray
Ozgurtas, Taner
Yalta, Tulın D.
Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model
title Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model
title_full Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model
title_fullStr Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model
title_full_unstemmed Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model
title_short Sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model
title_sort sesamin ameliorates mucosal tissue injury of mesenteric ischemia and reperfusion in an experimental rat model
topic Experimental Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855156/
https://www.ncbi.nlm.nih.gov/pubmed/31749888
http://dx.doi.org/10.5114/aoms.2017.68535
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