Effect of Prostaglandin E-1 on Wisconsin University and Histidine-Tryptophan-Ketoglutarate Preservation Solutions on Preservation Injury of the Perfused Liver

Abstract Background The aim of this study was to investigate the effects of prostaglandin E-1 (PGE-1) on preservation injury in livers perfused with the University of Wisconsin (UW) or histidine-tryptophan-ketoglutarate (HTK) solutions. Materials and methods Five groups each including six rats inclu...

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Veröffentlicht in:Transplantation proceedings 2013-07, Vol.45 (6), p.2446-2450
Hauptverfasser: Aliosmanoglu, I, Sevmis, S, Karakayali, H, Kocbiyik, A, Dagdeviren, A, Haberal, A, Haberal, M
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container_end_page 2450
container_issue 6
container_start_page 2446
container_title Transplantation proceedings
container_volume 45
creator Aliosmanoglu, I
Sevmis, S
Karakayali, H
Kocbiyik, A
Dagdeviren, A
Haberal, A
Haberal, M
description Abstract Background The aim of this study was to investigate the effects of prostaglandin E-1 (PGE-1) on preservation injury in livers perfused with the University of Wisconsin (UW) or histidine-tryptophan-ketoglutarate (HTK) solutions. Materials and methods Five groups each including six rats included. Ringer’s lactate RL (group 1), HTK (group 2), HTK + PGE-1 (group 3), UW (group 4), or UW PGE-1 (group 5). Liver tissue and preservation fluid samples were obtained from the perfused lives for pathological and biochemical examinations respectively at 0, 6 and 12 hours. Results Upon biochemical examination, aspartate aminotrasnferase and alanine aminotransferase values were highest among the group with RL solution and lowest with PGE-1. Liver structure was found to be damaged immediately after RL solution, whereas it was preserved in the other four groups. Fewer cellular changes were reported at the end of 12 hours in the groups administered PGE-1 compared with the other groups. Conclusions PGE-1 when applied before preservation protected liver functions, decreased pathologic injury, and delayed changes that occur under cold ischemic conditions.
doi_str_mv 10.1016/j.transproceed.2012.05.093
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Materials and methods Five groups each including six rats included. Ringer’s lactate RL (group 1), HTK (group 2), HTK + PGE-1 (group 3), UW (group 4), or UW PGE-1 (group 5). Liver tissue and preservation fluid samples were obtained from the perfused lives for pathological and biochemical examinations respectively at 0, 6 and 12 hours. Results Upon biochemical examination, aspartate aminotrasnferase and alanine aminotransferase values were highest among the group with RL solution and lowest with PGE-1. Liver structure was found to be damaged immediately after RL solution, whereas it was preserved in the other four groups. Fewer cellular changes were reported at the end of 12 hours in the groups administered PGE-1 compared with the other groups. Conclusions PGE-1 when applied before preservation protected liver functions, decreased pathologic injury, and delayed changes that occur under cold ischemic conditions.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2012.05.093</identifier><identifier>PMID: 23871184</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenosine - pharmacology ; Alanine Transaminase - metabolism ; Allopurinol - pharmacology ; Alprostadil - pharmacology ; Animals ; Aspartate Aminotransferases - metabolism ; Biomarkers - metabolism ; Cold Ischemia - adverse effects ; Cytoprotection ; Glucose - pharmacology ; Glutathione - pharmacology ; Hepatectomy ; Insulin - pharmacology ; Isotonic Solutions - pharmacology ; Liver - blood supply ; Liver - drug effects ; Liver - enzymology ; Liver - pathology ; Male ; Mannitol - pharmacology ; Organ Preservation - methods ; Organ Preservation Solutions - pharmacology ; Perfusion ; Potassium Chloride - pharmacology ; Procaine - pharmacology ; Raffinose - pharmacology ; Rats ; Rats, Wistar ; Reperfusion Injury - etiology ; Reperfusion Injury - metabolism ; Reperfusion Injury - pathology ; Reperfusion Injury - prevention &amp; control ; Surgery ; Time Factors</subject><ispartof>Transplantation proceedings, 2013-07, Vol.45 (6), p.2446-2450</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-649619c66ae801247bb64da91d537ca219c0f9d9f1bd0770567d2ce94cf734703</citedby><cites>FETCH-LOGICAL-c435t-649619c66ae801247bb64da91d537ca219c0f9d9f1bd0770567d2ce94cf734703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0041134512012973$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23871184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aliosmanoglu, I</creatorcontrib><creatorcontrib>Sevmis, S</creatorcontrib><creatorcontrib>Karakayali, H</creatorcontrib><creatorcontrib>Kocbiyik, A</creatorcontrib><creatorcontrib>Dagdeviren, A</creatorcontrib><creatorcontrib>Haberal, A</creatorcontrib><creatorcontrib>Haberal, M</creatorcontrib><title>Effect of Prostaglandin E-1 on Wisconsin University and Histidine-Tryptophan-Ketoglutarate Preservation Solutions on Preservation Injury of the Perfused Liver</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Abstract Background The aim of this study was to investigate the effects of prostaglandin E-1 (PGE-1) on preservation injury in livers perfused with the University of Wisconsin (UW) or histidine-tryptophan-ketoglutarate (HTK) solutions. Materials and methods Five groups each including six rats included. Ringer’s lactate RL (group 1), HTK (group 2), HTK + PGE-1 (group 3), UW (group 4), or UW PGE-1 (group 5). Liver tissue and preservation fluid samples were obtained from the perfused lives for pathological and biochemical examinations respectively at 0, 6 and 12 hours. Results Upon biochemical examination, aspartate aminotrasnferase and alanine aminotransferase values were highest among the group with RL solution and lowest with PGE-1. Liver structure was found to be damaged immediately after RL solution, whereas it was preserved in the other four groups. Fewer cellular changes were reported at the end of 12 hours in the groups administered PGE-1 compared with the other groups. Conclusions PGE-1 when applied before preservation protected liver functions, decreased pathologic injury, and delayed changes that occur under cold ischemic conditions.</description><subject>Adenosine - pharmacology</subject><subject>Alanine Transaminase - metabolism</subject><subject>Allopurinol - pharmacology</subject><subject>Alprostadil - pharmacology</subject><subject>Animals</subject><subject>Aspartate Aminotransferases - metabolism</subject><subject>Biomarkers - metabolism</subject><subject>Cold Ischemia - adverse effects</subject><subject>Cytoprotection</subject><subject>Glucose - pharmacology</subject><subject>Glutathione - pharmacology</subject><subject>Hepatectomy</subject><subject>Insulin - pharmacology</subject><subject>Isotonic Solutions - pharmacology</subject><subject>Liver - blood supply</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>Liver - pathology</subject><subject>Male</subject><subject>Mannitol - pharmacology</subject><subject>Organ Preservation - methods</subject><subject>Organ Preservation Solutions - pharmacology</subject><subject>Perfusion</subject><subject>Potassium Chloride - pharmacology</subject><subject>Procaine - pharmacology</subject><subject>Raffinose - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reperfusion Injury - etiology</subject><subject>Reperfusion Injury - metabolism</subject><subject>Reperfusion Injury - pathology</subject><subject>Reperfusion Injury - prevention &amp; control</subject><subject>Surgery</subject><subject>Time Factors</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUsFu1DAQtRCILoVfQBEnLgl27MQbDkioLLRiJZDaiqPltSetl6y9tZ2V8jXwLXwZE20rASdOtmfevPG8N4S8YrRilLVvtlWO2qd9DAbAVjVldUWbinb8EVmwpeRl3db8MVlQKljJuGhOyLOUthTfteBPyUnNl5KxpViQH6u-B5OL0BdfY0hZ3wzaW-eLVcmK4ItvLpngEwauvTtATC5PBSKKc5eyQyCUV3Ha57C_1b78DDncDGPWUWdAQkgQDzo7JLoMGMdLQtZfP_9KXfjtGKf5C_kWqyD2YwJbrOd-z8mTXg8JXtyfp-T64-rq7Lxcf_l0cfZ-XRrBm1y2omtZZ9pWwxLlEHKzaYXVHbMNl0bXmKN9Z7uebSyVkjattLWBTpheciEpPyWvj7yo6t0IKasdTg4DqgFhTIqJum2Y5LRF6Nsj1KBgKUKv9tHtdJwUo2o2SG3Vnwap2SBFG4UGYfHL-z7jZoe5h9IHRxDw4QgAnPbgIKpkHHgD1kU0Stng_q_Pu39ozOC8M3r4DhOkbRijRz0VUwlr1OW8KvOmsJmkk5z_BnDuwek</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Aliosmanoglu, I</creator><creator>Sevmis, S</creator><creator>Karakayali, H</creator><creator>Kocbiyik, A</creator><creator>Dagdeviren, A</creator><creator>Haberal, A</creator><creator>Haberal, M</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>20130701</creationdate><title>Effect of Prostaglandin E-1 on Wisconsin University and Histidine-Tryptophan-Ketoglutarate Preservation Solutions on Preservation Injury of the Perfused Liver</title><author>Aliosmanoglu, I ; Sevmis, S ; Karakayali, H ; Kocbiyik, A ; Dagdeviren, A ; Haberal, A ; Haberal, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-649619c66ae801247bb64da91d537ca219c0f9d9f1bd0770567d2ce94cf734703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenosine - pharmacology</topic><topic>Alanine Transaminase - metabolism</topic><topic>Allopurinol - pharmacology</topic><topic>Alprostadil - pharmacology</topic><topic>Animals</topic><topic>Aspartate Aminotransferases - metabolism</topic><topic>Biomarkers - metabolism</topic><topic>Cold Ischemia - adverse effects</topic><topic>Cytoprotection</topic><topic>Glucose - pharmacology</topic><topic>Glutathione - pharmacology</topic><topic>Hepatectomy</topic><topic>Insulin - pharmacology</topic><topic>Isotonic Solutions - pharmacology</topic><topic>Liver - blood supply</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>Liver - pathology</topic><topic>Male</topic><topic>Mannitol - pharmacology</topic><topic>Organ Preservation - methods</topic><topic>Organ Preservation Solutions - pharmacology</topic><topic>Perfusion</topic><topic>Potassium Chloride - pharmacology</topic><topic>Procaine - pharmacology</topic><topic>Raffinose - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reperfusion Injury - etiology</topic><topic>Reperfusion Injury - metabolism</topic><topic>Reperfusion Injury - pathology</topic><topic>Reperfusion Injury - prevention &amp; control</topic><topic>Surgery</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aliosmanoglu, I</creatorcontrib><creatorcontrib>Sevmis, S</creatorcontrib><creatorcontrib>Karakayali, H</creatorcontrib><creatorcontrib>Kocbiyik, A</creatorcontrib><creatorcontrib>Dagdeviren, A</creatorcontrib><creatorcontrib>Haberal, A</creatorcontrib><creatorcontrib>Haberal, M</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>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aliosmanoglu, I</au><au>Sevmis, S</au><au>Karakayali, H</au><au>Kocbiyik, A</au><au>Dagdeviren, A</au><au>Haberal, A</au><au>Haberal, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Prostaglandin E-1 on Wisconsin University and Histidine-Tryptophan-Ketoglutarate Preservation Solutions on Preservation Injury of the Perfused Liver</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>45</volume><issue>6</issue><spage>2446</spage><epage>2450</epage><pages>2446-2450</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><abstract>Abstract Background The aim of this study was to investigate the effects of prostaglandin E-1 (PGE-1) on preservation injury in livers perfused with the University of Wisconsin (UW) or histidine-tryptophan-ketoglutarate (HTK) solutions. Materials and methods Five groups each including six rats included. Ringer’s lactate RL (group 1), HTK (group 2), HTK + PGE-1 (group 3), UW (group 4), or UW PGE-1 (group 5). Liver tissue and preservation fluid samples were obtained from the perfused lives for pathological and biochemical examinations respectively at 0, 6 and 12 hours. Results Upon biochemical examination, aspartate aminotrasnferase and alanine aminotransferase values were highest among the group with RL solution and lowest with PGE-1. Liver structure was found to be damaged immediately after RL solution, whereas it was preserved in the other four groups. Fewer cellular changes were reported at the end of 12 hours in the groups administered PGE-1 compared with the other groups. Conclusions PGE-1 when applied before preservation protected liver functions, decreased pathologic injury, and delayed changes that occur under cold ischemic conditions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23871184</pmid><doi>10.1016/j.transproceed.2012.05.093</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adenosine - pharmacology
Alanine Transaminase - metabolism
Allopurinol - pharmacology
Alprostadil - pharmacology
Animals
Aspartate Aminotransferases - metabolism
Biomarkers - metabolism
Cold Ischemia - adverse effects
Cytoprotection
Glucose - pharmacology
Glutathione - pharmacology
Hepatectomy
Insulin - pharmacology
Isotonic Solutions - pharmacology
Liver - blood supply
Liver - drug effects
Liver - enzymology
Liver - pathology
Male
Mannitol - pharmacology
Organ Preservation - methods
Organ Preservation Solutions - pharmacology
Perfusion
Potassium Chloride - pharmacology
Procaine - pharmacology
Raffinose - pharmacology
Rats
Rats, Wistar
Reperfusion Injury - etiology
Reperfusion Injury - metabolism
Reperfusion Injury - pathology
Reperfusion Injury - prevention & control
Surgery
Time Factors
title Effect of Prostaglandin E-1 on Wisconsin University and Histidine-Tryptophan-Ketoglutarate Preservation Solutions on Preservation Injury of the Perfused Liver
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