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Protective effects of pentoxifylline in small intestine after ischemia–reperfusion
OBJECTIVE: This study was performed to determine the healing effects of pentoxifylline on molecular responses and protection against severe ischemic damage in the small intestine. METHODS: Thirty-six Wistar albino rats were divided into six groups. The superior mesenteric artery was clamped for 120...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166353/ https://www.ncbi.nlm.nih.gov/pubmed/30027781 http://dx.doi.org/10.1177/0300060518786904 |
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author | Eğin, Seracettin İlhan, Mehmet Bademler, Süleyman Gökçek, Berk Hot, Semih Ekmekçi, Hakan Ekmekçi, Özlem Balcı Tanrıverdi, Gamze Dağıstanlı, Fatma Kaya Kamalı, Gülçin Kamalı, Sedat Güloğlu, Recep |
author_facet | Eğin, Seracettin İlhan, Mehmet Bademler, Süleyman Gökçek, Berk Hot, Semih Ekmekçi, Hakan Ekmekçi, Özlem Balcı Tanrıverdi, Gamze Dağıstanlı, Fatma Kaya Kamalı, Gülçin Kamalı, Sedat Güloğlu, Recep |
author_sort | Eğin, Seracettin |
collection | PubMed |
description | OBJECTIVE: This study was performed to determine the healing effects of pentoxifylline on molecular responses and protection against severe ischemic damage in the small intestine. METHODS: Thirty-six Wistar albino rats were divided into six groups. The superior mesenteric artery was clamped for 120 minutes, and reperfusion was performed for 60 minutes. Saline (0.4 mL), pentoxifylline (1 mg/kg), and pentoxifylline (10 mg/kg) were intraperitoneally administered to the rats in the C(1), P(1), and P(3) groups, respectively, 60 minutes before ischemia and to the rats in the C(2), P(2), and P(4) groups, respectively, during reperfusion onset. Malondialdehyde, myeloperoxidase, tumor necrosis factor alpha, interleukin-1 beta, and interleukin-6 in serum and tissue were measured by enzyme-linked immunosorbent assay. Intestinal ischemic injury was histopathologically evaluated by the Chiu score and immunohistochemical staining. RESULTS: All serum and tissue molecular responses were significantly blunted in the pentoxifylline-treated groups compared with the controls. Significant improvement in ischemic damage was demonstrated in the pentoxifylline-treated groups by histological grading and immunohistochemical scoring. CONCLUSIONS: The protective effects of pentoxifylline were confirmed by molecular responses and histopathological examination. |
format | Online Article Text |
id | pubmed-6166353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61663532018-10-03 Protective effects of pentoxifylline in small intestine after ischemia–reperfusion Eğin, Seracettin İlhan, Mehmet Bademler, Süleyman Gökçek, Berk Hot, Semih Ekmekçi, Hakan Ekmekçi, Özlem Balcı Tanrıverdi, Gamze Dağıstanlı, Fatma Kaya Kamalı, Gülçin Kamalı, Sedat Güloğlu, Recep J Int Med Res Clinical Research Reports OBJECTIVE: This study was performed to determine the healing effects of pentoxifylline on molecular responses and protection against severe ischemic damage in the small intestine. METHODS: Thirty-six Wistar albino rats were divided into six groups. The superior mesenteric artery was clamped for 120 minutes, and reperfusion was performed for 60 minutes. Saline (0.4 mL), pentoxifylline (1 mg/kg), and pentoxifylline (10 mg/kg) were intraperitoneally administered to the rats in the C(1), P(1), and P(3) groups, respectively, 60 minutes before ischemia and to the rats in the C(2), P(2), and P(4) groups, respectively, during reperfusion onset. Malondialdehyde, myeloperoxidase, tumor necrosis factor alpha, interleukin-1 beta, and interleukin-6 in serum and tissue were measured by enzyme-linked immunosorbent assay. Intestinal ischemic injury was histopathologically evaluated by the Chiu score and immunohistochemical staining. RESULTS: All serum and tissue molecular responses were significantly blunted in the pentoxifylline-treated groups compared with the controls. Significant improvement in ischemic damage was demonstrated in the pentoxifylline-treated groups by histological grading and immunohistochemical scoring. CONCLUSIONS: The protective effects of pentoxifylline were confirmed by molecular responses and histopathological examination. SAGE Publications 2018-07-20 2018-10 /pmc/articles/PMC6166353/ /pubmed/30027781 http://dx.doi.org/10.1177/0300060518786904 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Research Reports Eğin, Seracettin İlhan, Mehmet Bademler, Süleyman Gökçek, Berk Hot, Semih Ekmekçi, Hakan Ekmekçi, Özlem Balcı Tanrıverdi, Gamze Dağıstanlı, Fatma Kaya Kamalı, Gülçin Kamalı, Sedat Güloğlu, Recep Protective effects of pentoxifylline in small intestine after ischemia–reperfusion |
title | Protective effects of pentoxifylline in small intestine after
ischemia–reperfusion |
title_full | Protective effects of pentoxifylline in small intestine after
ischemia–reperfusion |
title_fullStr | Protective effects of pentoxifylline in small intestine after
ischemia–reperfusion |
title_full_unstemmed | Protective effects of pentoxifylline in small intestine after
ischemia–reperfusion |
title_short | Protective effects of pentoxifylline in small intestine after
ischemia–reperfusion |
title_sort | protective effects of pentoxifylline in small intestine after
ischemia–reperfusion |
topic | Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166353/ https://www.ncbi.nlm.nih.gov/pubmed/30027781 http://dx.doi.org/10.1177/0300060518786904 |
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