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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
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.
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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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