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Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats

BACKGROUND AND AIM: Ischemia/reperfusion (I/R) injury in the liver occurs after a prolonged period of ischemia followed by restoration of hepatic blood perfusion. During the surgery of abdominal aorta, I/R injury causes damage to lower extremities and many organs, especially liver. The antioxidant a...

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Autores principales: Cure, Erkan, Cure, Medine C., Tumkaya, Levent, Kalkan, Yildiray, Aydin, Ibrahim, Kirbas, Aynur, Yilmaz, Arif, Yuce, Suleyman, Gokce, Mehmet F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196345/
https://www.ncbi.nlm.nih.gov/pubmed/25253365
http://dx.doi.org/10.4103/1319-3767.141690
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author Cure, Erkan
Cure, Medine C.
Tumkaya, Levent
Kalkan, Yildiray
Aydin, Ibrahim
Kirbas, Aynur
Yilmaz, Arif
Yuce, Suleyman
Gokce, Mehmet F.
author_facet Cure, Erkan
Cure, Medine C.
Tumkaya, Levent
Kalkan, Yildiray
Aydin, Ibrahim
Kirbas, Aynur
Yilmaz, Arif
Yuce, Suleyman
Gokce, Mehmet F.
author_sort Cure, Erkan
collection PubMed
description BACKGROUND AND AIM: Ischemia/reperfusion (I/R) injury in the liver occurs after a prolonged period of ischemia followed by restoration of hepatic blood perfusion. During the surgery of abdominal aorta, I/R injury causes damage to lower extremities and many organs, especially liver. The antioxidant and tumor necrosis factor-alpha (TNF-α) suppression effects of topiramate (TPM) have been reported in several studies. We evaluated the potential protective effect of TPM on cellular damage in liver tissue during I/R injury. MATERIALS AND METHODS: Thirty male Wistar albino rats were divided into three groups: Control, I/R, and I/R plus TPM (I/R + TPM) groups. Laparotomy without I/R injury was performed in the control group. After laparotomy, cross-ligation of infrarenal abdominal aorta was applied for 2 h in I/R groups that was followed by 2 h of reperfusion. TPM (100 mg/kg/day) was orally administrated to the animals in the I/R + TPM group for seven consecutive days before I/R procedure. RESULTS: The I/R group's TNF-α and interleukin-6 (IL-6) levels were significantly higher than those of the control (P = 0.010; P = 0.002) and I/R + TPM groups (P = 0.010; P = 0.002, respectively). Asymmetric dimethyl arginine (ADMA) levels of I/R group were higher than the control (P = 0.015) and I/R + TPM groups. I/R caused serious histopathological damage to liver tissue; however, TPM led to very low histopathological changes. CONCLUSION: Our data demonstrated that TPM treatment prominently decreases the severity of liver I/R injury. TPM pretreatment may have preventive effects on liver injury via I/R during intra-abdominal surgery.
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spelling pubmed-41963452014-10-17 Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats Cure, Erkan Cure, Medine C. Tumkaya, Levent Kalkan, Yildiray Aydin, Ibrahim Kirbas, Aynur Yilmaz, Arif Yuce, Suleyman Gokce, Mehmet F. Saudi J Gastroenterol Original Article BACKGROUND AND AIM: Ischemia/reperfusion (I/R) injury in the liver occurs after a prolonged period of ischemia followed by restoration of hepatic blood perfusion. During the surgery of abdominal aorta, I/R injury causes damage to lower extremities and many organs, especially liver. The antioxidant and tumor necrosis factor-alpha (TNF-α) suppression effects of topiramate (TPM) have been reported in several studies. We evaluated the potential protective effect of TPM on cellular damage in liver tissue during I/R injury. MATERIALS AND METHODS: Thirty male Wistar albino rats were divided into three groups: Control, I/R, and I/R plus TPM (I/R + TPM) groups. Laparotomy without I/R injury was performed in the control group. After laparotomy, cross-ligation of infrarenal abdominal aorta was applied for 2 h in I/R groups that was followed by 2 h of reperfusion. TPM (100 mg/kg/day) was orally administrated to the animals in the I/R + TPM group for seven consecutive days before I/R procedure. RESULTS: The I/R group's TNF-α and interleukin-6 (IL-6) levels were significantly higher than those of the control (P = 0.010; P = 0.002) and I/R + TPM groups (P = 0.010; P = 0.002, respectively). Asymmetric dimethyl arginine (ADMA) levels of I/R group were higher than the control (P = 0.015) and I/R + TPM groups. I/R caused serious histopathological damage to liver tissue; however, TPM led to very low histopathological changes. CONCLUSION: Our data demonstrated that TPM treatment prominently decreases the severity of liver I/R injury. TPM pretreatment may have preventive effects on liver injury via I/R during intra-abdominal surgery. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4196345/ /pubmed/25253365 http://dx.doi.org/10.4103/1319-3767.141690 Text en Copyright: © Saudi Journal of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cure, Erkan
Cure, Medine C.
Tumkaya, Levent
Kalkan, Yildiray
Aydin, Ibrahim
Kirbas, Aynur
Yilmaz, Arif
Yuce, Suleyman
Gokce, Mehmet F.
Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats
title Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats
title_full Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats
title_fullStr Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats
title_full_unstemmed Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats
title_short Topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats
title_sort topiramate ameliorates abdominal aorta cross-clamping induced liver injury in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196345/
https://www.ncbi.nlm.nih.gov/pubmed/25253365
http://dx.doi.org/10.4103/1319-3767.141690
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