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Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis
BACKGROUND: Acute respiratory distress syndrome is a devastating complication of severe sepsis. Preclinical models suggest that direct lung injury begins with attack to the lung epithelium, but indirect lung injury results from systemic endothelial damage due to inflammatory mediators. The aim of th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443160/ https://www.ncbi.nlm.nih.gov/pubmed/34967421 http://dx.doi.org/10.14744/tjtes.2020.02589 |
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author | Bora, Ejder Saylav Erdoğan, Arife Alper Erdoğan, Mumin Yigitturk, Gurkan Çakır, Adem Erbaş, Oytun |
author_facet | Bora, Ejder Saylav Erdoğan, Arife Alper Erdoğan, Mumin Yigitturk, Gurkan Çakır, Adem Erbaş, Oytun |
author_sort | Bora, Ejder Saylav |
collection | PubMed |
description | BACKGROUND: Acute respiratory distress syndrome is a devastating complication of severe sepsis. Preclinical models suggest that direct lung injury begins with attack to the lung epithelium, but indirect lung injury results from systemic endothelial damage due to inflammatory mediators. The aim of the present study was to explore the effect of octreotide on lungs in a surgically induced sepsis model in rats. METHODS: We used 32 male Sprague Dawley rats and divided into four groups. Group 1: Normal (non-operative and orally fed control, n=8); Group 2: Sham operated (n=8); Group 3: Cecal ligation and puncture (CLP) (untreated group, n=8); and Group 4: CLP and 100 μg/kg octreotide i.p. (n=8). For sepsis, CLP procedure was performed on 16 rats to induce a sepsis model. All groups were analyzed, their blood was taken for arterial blood gas analysis. For histological examination, lung tissues were removed and sections were prepared. RESULTS: In histological examination, if we compare CLP + Octreotide with only CLP group in CLP + Octreotide group decreased inflammatory cell infiltration in alveolar and interstitial area as well as edema, bleeding, when CLP group was compared with octreotide group, all histopathological parameters improved significantly and the severity index decreased from 3 to 1. For arterial blood gas, when CLP and octreotide groups were compared with CLP group, it was observed that there was a significant change in favor of healing and that they almost came up to controls and sham group. CONCLUSION: It could be hypothesized that it would be beneficial to administer octreotide for ameliorate lung injury state in sepsis patients. |
format | Online Article Text |
id | pubmed-10443160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-104431602023-08-23 Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis Bora, Ejder Saylav Erdoğan, Arife Alper Erdoğan, Mumin Yigitturk, Gurkan Çakır, Adem Erbaş, Oytun Ulus Travma Acil Cerrahi Derg Experimental Study BACKGROUND: Acute respiratory distress syndrome is a devastating complication of severe sepsis. Preclinical models suggest that direct lung injury begins with attack to the lung epithelium, but indirect lung injury results from systemic endothelial damage due to inflammatory mediators. The aim of the present study was to explore the effect of octreotide on lungs in a surgically induced sepsis model in rats. METHODS: We used 32 male Sprague Dawley rats and divided into four groups. Group 1: Normal (non-operative and orally fed control, n=8); Group 2: Sham operated (n=8); Group 3: Cecal ligation and puncture (CLP) (untreated group, n=8); and Group 4: CLP and 100 μg/kg octreotide i.p. (n=8). For sepsis, CLP procedure was performed on 16 rats to induce a sepsis model. All groups were analyzed, their blood was taken for arterial blood gas analysis. For histological examination, lung tissues were removed and sections were prepared. RESULTS: In histological examination, if we compare CLP + Octreotide with only CLP group in CLP + Octreotide group decreased inflammatory cell infiltration in alveolar and interstitial area as well as edema, bleeding, when CLP group was compared with octreotide group, all histopathological parameters improved significantly and the severity index decreased from 3 to 1. For arterial blood gas, when CLP and octreotide groups were compared with CLP group, it was observed that there was a significant change in favor of healing and that they almost came up to controls and sham group. CONCLUSION: It could be hypothesized that it would be beneficial to administer octreotide for ameliorate lung injury state in sepsis patients. Kare Publishing 2022-01-03 /pmc/articles/PMC10443160/ /pubmed/34967421 http://dx.doi.org/10.14744/tjtes.2020.02589 Text en Copyright © 2022 Turkish Journal of Trauma and Emergency Surgery https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Experimental Study Bora, Ejder Saylav Erdoğan, Arife Alper Erdoğan, Mumin Yigitturk, Gurkan Çakır, Adem Erbaş, Oytun Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis |
title | Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis |
title_full | Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis |
title_fullStr | Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis |
title_full_unstemmed | Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis |
title_short | Short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis |
title_sort | short-term protective effect of octreotide on the lungs of rats with experimentally induced sepsis |
topic | Experimental Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443160/ https://www.ncbi.nlm.nih.gov/pubmed/34967421 http://dx.doi.org/10.14744/tjtes.2020.02589 |
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