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Protective effect of erythropoietin on torsion/detorsion injury in rat model

Abstract Purpose The aim of the study is to investigate the effects of erythropoietin on torsion/detorsion injury in rats. Methods Forty rats were divided randomly into 5 groups: group I (sham, S), sham operation; group II (torsion/detorsion 1, T/D1 ), 3 hours ischemia and 1 hour reperfusion; group...

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Published in:Journal of pediatric surgery 2009-10, Vol.44 (10), p.1988-1994
Main Authors: Bakan, Vedat, Çıralık, Harun, Tolun, Fatma İnanaç, Atlı, Yalçın, Mil, Ayhan, Öztürk, Şenol
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cited_by cdi_FETCH-LOGICAL-c422t-7350e799e0045c10a79eb70bf096fd57eecc42fee1b758772c76ba375e5c89933
cites cdi_FETCH-LOGICAL-c422t-7350e799e0045c10a79eb70bf096fd57eecc42fee1b758772c76ba375e5c89933
container_end_page 1994
container_issue 10
container_start_page 1988
container_title Journal of pediatric surgery
container_volume 44
creator Bakan, Vedat
Çıralık, Harun
Tolun, Fatma İnanaç
Atlı, Yalçın
Mil, Ayhan
Öztürk, Şenol
description Abstract Purpose The aim of the study is to investigate the effects of erythropoietin on torsion/detorsion injury in rats. Methods Forty rats were divided randomly into 5 groups: group I (sham, S), sham operation; group II (torsion/detorsion 1, T/D1 ), 3 hours ischemia and 1 hour reperfusion; group III (torsion/detorsion 2, T/D2 ), 3 hours ischemia and 48 hours reperfusion; group IV (erythropoietin 1, EPO1 ), 3 hours ischemia, 1 hour reperfusion, and a single dose of EPO; and group V (erythropoietin 2, EPO2 ), 3 hours ischemia, 48 hours reperfusion, and 2 doses of EPO. Malondialdehyde (MDA) and nitric oxide (NO) levels and activities of superoxide dismutase and catalase were measured. Tissue damage to ovarian tissue was scored by histologic examination. Data were compared among groups with parametric tests. Results The MDA levels in the S and EPO groups were significantly lower than the T/D groups ( P   .05). Conclusion Erythropoietin attenuates ischemia-reperfusion injury when given during the acute phase of ovarian torsion-detorsion in a rat model.
doi_str_mv 10.1016/j.jpedsurg.2009.02.071
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Methods Forty rats were divided randomly into 5 groups: group I (sham, S), sham operation; group II (torsion/detorsion 1, T/D1 ), 3 hours ischemia and 1 hour reperfusion; group III (torsion/detorsion 2, T/D2 ), 3 hours ischemia and 48 hours reperfusion; group IV (erythropoietin 1, EPO1 ), 3 hours ischemia, 1 hour reperfusion, and a single dose of EPO; and group V (erythropoietin 2, EPO2 ), 3 hours ischemia, 48 hours reperfusion, and 2 doses of EPO. Malondialdehyde (MDA) and nitric oxide (NO) levels and activities of superoxide dismutase and catalase were measured. Tissue damage to ovarian tissue was scored by histologic examination. Data were compared among groups with parametric tests. Results The MDA levels in the S and EPO groups were significantly lower than the T/D groups ( P  &lt; .001). Catalase and superoxide dismutase activities, and NO levels in the S and EPO groups were significantly higher than in the T/D groups ( P &lt; .05). Ovarian tissue damage in the S and EPO groups was significantly less than in the T/D groups ( P &lt; .05). Levels of all biochemical markers and ovarian tissue damage scores were similar among the S, EPO1 , and EPO2 groups ( P &gt; .05). Conclusion Erythropoietin attenuates ischemia-reperfusion injury when given during the acute phase of ovarian torsion-detorsion in a rat model.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/j.jpedsurg.2009.02.071</identifier><identifier>PMID: 19853760</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antioxidants - therapeutic use ; Catalase - metabolism ; Disease Models, Animal ; Erythropoietin ; Erythropoietin - therapeutic use ; Female ; Ischemia-reperfusion ; Malondialdehyde - metabolism ; Nitric Oxide - metabolism ; Ovarian Diseases - metabolism ; Ovarian Diseases - pathology ; Ovarian Diseases - prevention &amp; control ; Ovarian torsion-detorsion ; Ovary - metabolism ; Ovary - pathology ; Pediatrics ; Random Allocation ; Rats ; Rats, Sprague-Dawley ; Recombinant Proteins ; Reperfusion Injury - metabolism ; Reperfusion Injury - pathology ; Reperfusion Injury - prevention &amp; control ; Superoxide Dismutase - metabolism ; Surgery ; Torsion Abnormality - drug therapy ; Torsion Abnormality - metabolism ; Torsion Abnormality - pathology ; Torsion Abnormality - prevention &amp; control</subject><ispartof>Journal of pediatric surgery, 2009-10, Vol.44 (10), p.1988-1994</ispartof><rights>Elsevier Inc.</rights><rights>2009 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-7350e799e0045c10a79eb70bf096fd57eecc42fee1b758772c76ba375e5c89933</citedby><cites>FETCH-LOGICAL-c422t-7350e799e0045c10a79eb70bf096fd57eecc42fee1b758772c76ba375e5c89933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19853760$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bakan, Vedat</creatorcontrib><creatorcontrib>Çıralık, Harun</creatorcontrib><creatorcontrib>Tolun, Fatma İnanaç</creatorcontrib><creatorcontrib>Atlı, Yalçın</creatorcontrib><creatorcontrib>Mil, Ayhan</creatorcontrib><creatorcontrib>Öztürk, Şenol</creatorcontrib><title>Protective effect of erythropoietin on torsion/detorsion injury in rat model</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Abstract Purpose The aim of the study is to investigate the effects of erythropoietin on torsion/detorsion injury in rats. Methods Forty rats were divided randomly into 5 groups: group I (sham, S), sham operation; group II (torsion/detorsion 1, T/D1 ), 3 hours ischemia and 1 hour reperfusion; group III (torsion/detorsion 2, T/D2 ), 3 hours ischemia and 48 hours reperfusion; group IV (erythropoietin 1, EPO1 ), 3 hours ischemia, 1 hour reperfusion, and a single dose of EPO; and group V (erythropoietin 2, EPO2 ), 3 hours ischemia, 48 hours reperfusion, and 2 doses of EPO. Malondialdehyde (MDA) and nitric oxide (NO) levels and activities of superoxide dismutase and catalase were measured. Tissue damage to ovarian tissue was scored by histologic examination. Data were compared among groups with parametric tests. Results The MDA levels in the S and EPO groups were significantly lower than the T/D groups ( P  &lt; .001). Catalase and superoxide dismutase activities, and NO levels in the S and EPO groups were significantly higher than in the T/D groups ( P &lt; .05). Ovarian tissue damage in the S and EPO groups was significantly less than in the T/D groups ( P &lt; .05). Levels of all biochemical markers and ovarian tissue damage scores were similar among the S, EPO1 , and EPO2 groups ( P &gt; .05). 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control</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Surgery</subject><subject>Torsion Abnormality - drug therapy</subject><subject>Torsion Abnormality - metabolism</subject><subject>Torsion Abnormality - pathology</subject><subject>Torsion Abnormality - prevention &amp; control</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkU9LxDAQxYMouq5-BenNU7uTZNNsLqKI_2BBQT2HNp1qardZk1bYb2_KrghePM0wvDfD-w0hZxQyCjSfNVmzxioM_i1jACoDloGke2RCBaepAC73yQSAsZTP88UROQ6hAYhjoIfkiKqF4DKHCVk-edej6e0XJljXsUtcnaDf9O_erZ3F3naJ65Le-WBdN6tw1yW2awa_iSXxRZ-sXIXtCTmoizbg6a5Oyevtzcv1fbp8vHu4vlqmZs5Yn0ouAKVSCDAXhkIhFZYSyhpUXldCIpoorBFpKcVCSmZkXhZcChRmoRTnU3K-3bv27nPA0OuVDQbbtujQDUFLPh8hxYxTkm-VxrsQPNZ67e2q8BtNQY8a3egfkHoEqYHpCDIaz3YnhnKF1a9tRy4KLrcCjEG_LHodjMXOYGV9pKgrZ_-_cfFnhWltZ03RfuAGQ-MG30WMmuoQDfp5fOf4TVAAVEjGvwGtJZ2I</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Bakan, Vedat</creator><creator>Çıralık, Harun</creator><creator>Tolun, Fatma İnanaç</creator><creator>Atlı, Yalçın</creator><creator>Mil, Ayhan</creator><creator>Öztürk, Şenol</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20091001</creationdate><title>Protective effect of erythropoietin on torsion/detorsion injury in rat model</title><author>Bakan, Vedat ; Çıralık, Harun ; Tolun, Fatma İnanaç ; Atlı, Yalçın ; Mil, Ayhan ; Öztürk, Şenol</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-7350e799e0045c10a79eb70bf096fd57eecc42fee1b758772c76ba375e5c89933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Antioxidants - therapeutic use</topic><topic>Catalase - metabolism</topic><topic>Disease Models, Animal</topic><topic>Erythropoietin</topic><topic>Erythropoietin - therapeutic use</topic><topic>Female</topic><topic>Ischemia-reperfusion</topic><topic>Malondialdehyde - metabolism</topic><topic>Nitric Oxide - metabolism</topic><topic>Ovarian Diseases - metabolism</topic><topic>Ovarian Diseases - pathology</topic><topic>Ovarian Diseases - prevention &amp; control</topic><topic>Ovarian torsion-detorsion</topic><topic>Ovary - metabolism</topic><topic>Ovary - pathology</topic><topic>Pediatrics</topic><topic>Random Allocation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Recombinant Proteins</topic><topic>Reperfusion Injury - metabolism</topic><topic>Reperfusion Injury - pathology</topic><topic>Reperfusion Injury - prevention &amp; control</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Surgery</topic><topic>Torsion Abnormality - drug therapy</topic><topic>Torsion Abnormality - metabolism</topic><topic>Torsion Abnormality - pathology</topic><topic>Torsion Abnormality - prevention &amp; control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bakan, Vedat</creatorcontrib><creatorcontrib>Çıralık, Harun</creatorcontrib><creatorcontrib>Tolun, Fatma İnanaç</creatorcontrib><creatorcontrib>Atlı, Yalçın</creatorcontrib><creatorcontrib>Mil, Ayhan</creatorcontrib><creatorcontrib>Öztürk, Şenol</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bakan, Vedat</au><au>Çıralık, Harun</au><au>Tolun, Fatma İnanaç</au><au>Atlı, Yalçın</au><au>Mil, Ayhan</au><au>Öztürk, Şenol</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective effect of erythropoietin on torsion/detorsion injury in rat model</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>44</volume><issue>10</issue><spage>1988</spage><epage>1994</epage><pages>1988-1994</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>Abstract Purpose The aim of the study is to investigate the effects of erythropoietin on torsion/detorsion injury in rats. Methods Forty rats were divided randomly into 5 groups: group I (sham, S), sham operation; group II (torsion/detorsion 1, T/D1 ), 3 hours ischemia and 1 hour reperfusion; group III (torsion/detorsion 2, T/D2 ), 3 hours ischemia and 48 hours reperfusion; group IV (erythropoietin 1, EPO1 ), 3 hours ischemia, 1 hour reperfusion, and a single dose of EPO; and group V (erythropoietin 2, EPO2 ), 3 hours ischemia, 48 hours reperfusion, and 2 doses of EPO. Malondialdehyde (MDA) and nitric oxide (NO) levels and activities of superoxide dismutase and catalase were measured. Tissue damage to ovarian tissue was scored by histologic examination. Data were compared among groups with parametric tests. Results The MDA levels in the S and EPO groups were significantly lower than the T/D groups ( P  &lt; .001). Catalase and superoxide dismutase activities, and NO levels in the S and EPO groups were significantly higher than in the T/D groups ( P &lt; .05). Ovarian tissue damage in the S and EPO groups was significantly less than in the T/D groups ( P &lt; .05). Levels of all biochemical markers and ovarian tissue damage scores were similar among the S, EPO1 , and EPO2 groups ( P &gt; .05). Conclusion Erythropoietin attenuates ischemia-reperfusion injury when given during the acute phase of ovarian torsion-detorsion in a rat model.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19853760</pmid><doi>10.1016/j.jpedsurg.2009.02.071</doi><tpages>7</tpages></addata></record>
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subjects Animals
Antioxidants - therapeutic use
Catalase - metabolism
Disease Models, Animal
Erythropoietin
Erythropoietin - therapeutic use
Female
Ischemia-reperfusion
Malondialdehyde - metabolism
Nitric Oxide - metabolism
Ovarian Diseases - metabolism
Ovarian Diseases - pathology
Ovarian Diseases - prevention & control
Ovarian torsion-detorsion
Ovary - metabolism
Ovary - pathology
Pediatrics
Random Allocation
Rats
Rats, Sprague-Dawley
Recombinant Proteins
Reperfusion Injury - metabolism
Reperfusion Injury - pathology
Reperfusion Injury - prevention & control
Superoxide Dismutase - metabolism
Surgery
Torsion Abnormality - drug therapy
Torsion Abnormality - metabolism
Torsion Abnormality - pathology
Torsion Abnormality - prevention & control
title Protective effect of erythropoietin on torsion/detorsion injury in rat model
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