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Ischemic preconditioning protects against cold ischemic injury through an oxidative stress dependent mechanism
Background/Aims : Ischemic injury in cold preserved livers is characterized by sinusoidal endothelial cell (SEC) detachment and matrix metalloproteinase activity. Upon reperfusion reversible ischemic injury becomes permanent with SEC rapidly undergoing apoptosis. Ischemic preconditioning prevents re...
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Published in: | Journal of hepatology 2002, Vol.36 (1), p.78-84 |
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container_title | Journal of hepatology |
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creator | Sindram, David Rüdiger, Hannes A Upadhya, Aravinda G Strasberg, Steven M Clavien, Pierre-Alain |
description | Background/Aims
: Ischemic injury in cold preserved livers is characterized by sinusoidal endothelial cell (SEC) detachment and matrix metalloproteinase activity. Upon reperfusion reversible ischemic injury becomes permanent with SEC rapidly undergoing apoptosis. Ischemic preconditioning prevents reperfusion injury after normothermic ischemia. We hypothesized that ischemic preconditioning, through an oxygen free radical burst, protects against injury during cold preservation and reperfusion.
Methods
: Ischemic preconditioning was achieved in rats by clamping blood supply to the left and median lobes for 10
min followed by 15
min of reperfusion prior to preservation in cold University of Wisconsin solution for 30
h. In a second set of experiments, rats were pretreated with
N
-acetyl-cysteine (NAC). SEC apoptosis upon reperfusion was assessed in an isolated perfused rat liver (IPRL) model.
Results
: SEC detachment and activities of matrix metalloproteinase were significantly reduced in preconditioned livers. A decrease of SEC apoptosis after 1
h of reperfusion in the IPRL was noted in preconditioned livers compared to controls. Pretreatment with NAC reversed the beneficial effects of ischemic preconditioning on SEC detachment and apoptosis.
Conclusions
: Ischemic preconditioning is an effective strategy to prevent injury during cold preservation and after reperfusion. The protective effect is possibly mediated by oxygen free radicals. |
doi_str_mv | 10.1016/S0168-8278(01)00229-X |
format | article |
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: Ischemic injury in cold preserved livers is characterized by sinusoidal endothelial cell (SEC) detachment and matrix metalloproteinase activity. Upon reperfusion reversible ischemic injury becomes permanent with SEC rapidly undergoing apoptosis. Ischemic preconditioning prevents reperfusion injury after normothermic ischemia. We hypothesized that ischemic preconditioning, through an oxygen free radical burst, protects against injury during cold preservation and reperfusion.
Methods
: Ischemic preconditioning was achieved in rats by clamping blood supply to the left and median lobes for 10
min followed by 15
min of reperfusion prior to preservation in cold University of Wisconsin solution for 30
h. In a second set of experiments, rats were pretreated with
N
-acetyl-cysteine (NAC). SEC apoptosis upon reperfusion was assessed in an isolated perfused rat liver (IPRL) model.
Results
: SEC detachment and activities of matrix metalloproteinase were significantly reduced in preconditioned livers. A decrease of SEC apoptosis after 1
h of reperfusion in the IPRL was noted in preconditioned livers compared to controls. Pretreatment with NAC reversed the beneficial effects of ischemic preconditioning on SEC detachment and apoptosis.
Conclusions
: Ischemic preconditioning is an effective strategy to prevent injury during cold preservation and after reperfusion. The protective effect is possibly mediated by oxygen free radicals.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/S0168-8278(01)00229-X</identifier><identifier>PMID: 11804668</identifier><identifier>CODEN: JOHEEC</identifier><language>eng</language><publisher>Oxford: Elsevier B.V</publisher><subject>Animals ; Apoptosis ; Biological and medical sciences ; Cold preservation ; Cold Temperature ; Cryopreservation ; Digestive system ; Investigative techniques, diagnostic techniques (general aspects) ; Ischemia-reperfusion injury ; Ischemic Preconditioning ; Liver - metabolism ; Liver Transplantation ; Male ; Medical sciences ; Oxidative Stress - physiology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Rats ; Rats, Wistar ; Reperfusion Injury - metabolism</subject><ispartof>Journal of hepatology, 2002, Vol.36 (1), p.78-84</ispartof><rights>2002 European Association for the Study of the Liver</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c457t-7b6d709a9ae3282c794951b8f696752a33a1868b7a3ca631ea88049d53ee5d293</citedby><cites>FETCH-LOGICAL-c457t-7b6d709a9ae3282c794951b8f696752a33a1868b7a3ca631ea88049d53ee5d293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4023,27922,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13465698$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11804668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sindram, David</creatorcontrib><creatorcontrib>Rüdiger, Hannes A</creatorcontrib><creatorcontrib>Upadhya, Aravinda G</creatorcontrib><creatorcontrib>Strasberg, Steven M</creatorcontrib><creatorcontrib>Clavien, Pierre-Alain</creatorcontrib><title>Ischemic preconditioning protects against cold ischemic injury through an oxidative stress dependent mechanism</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Background/Aims
: Ischemic injury in cold preserved livers is characterized by sinusoidal endothelial cell (SEC) detachment and matrix metalloproteinase activity. Upon reperfusion reversible ischemic injury becomes permanent with SEC rapidly undergoing apoptosis. Ischemic preconditioning prevents reperfusion injury after normothermic ischemia. We hypothesized that ischemic preconditioning, through an oxygen free radical burst, protects against injury during cold preservation and reperfusion.
Methods
: Ischemic preconditioning was achieved in rats by clamping blood supply to the left and median lobes for 10
min followed by 15
min of reperfusion prior to preservation in cold University of Wisconsin solution for 30
h. In a second set of experiments, rats were pretreated with
N
-acetyl-cysteine (NAC). SEC apoptosis upon reperfusion was assessed in an isolated perfused rat liver (IPRL) model.
Results
: SEC detachment and activities of matrix metalloproteinase were significantly reduced in preconditioned livers. A decrease of SEC apoptosis after 1
h of reperfusion in the IPRL was noted in preconditioned livers compared to controls. Pretreatment with NAC reversed the beneficial effects of ischemic preconditioning on SEC detachment and apoptosis.
Conclusions
: Ischemic preconditioning is an effective strategy to prevent injury during cold preservation and after reperfusion. The protective effect is possibly mediated by oxygen free radicals.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Cold preservation</subject><subject>Cold Temperature</subject><subject>Cryopreservation</subject><subject>Digestive system</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Ischemia-reperfusion injury</subject><subject>Ischemic Preconditioning</subject><subject>Liver - metabolism</subject><subject>Liver Transplantation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Oxidative Stress - physiology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reperfusion Injury - metabolism</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkc9vFCEUgImxsdvqn6DhoqmHURgGBk6Naao2aeJBTXojb-HtLs0MswLTtP-9bHe1x14eecn3fn0Q8pazT5xx9flnDbrRba_PGP_IWNua5uYFWXDFWMNUx1-SxX_kmJzkfMsYE8x0r8gx55p1SukFiVfZbXAMjm4Tuin6UMIUQ1zXfCroSqawhhBzoW4aPA3_8BBv5_RAyyZN83pDIdLpPngo4Q5pLglzph63GD3GQkd0G4ghj6_J0QqGjG8O7yn5_fXy18X35vrHt6uLL9eN62Rfmn6pfM8MGEDR6tb1pjOSL_VKGdXLFoQArpVe9iAcKMERdD3IeCkQpW-NOCUf9n3rFX9mzMWOdXMcBog4zdn2vJOychWUe9ClKeeEK7tNYYT0YDmzO9H2UbTdWbSM20fR9qbWvTsMmJcj-qeqg9kKvD8AkB0MqwTRhfzEiU5JZXbc-Z7DquMuYLLZBYwOfagfUqyfwjOr_AXm6pyM</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Sindram, David</creator><creator>Rüdiger, Hannes A</creator><creator>Upadhya, Aravinda G</creator><creator>Strasberg, Steven M</creator><creator>Clavien, Pierre-Alain</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>2002</creationdate><title>Ischemic preconditioning protects against cold ischemic injury through an oxidative stress dependent mechanism</title><author>Sindram, David ; Rüdiger, Hannes A ; Upadhya, Aravinda G ; Strasberg, Steven M ; Clavien, Pierre-Alain</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c457t-7b6d709a9ae3282c794951b8f696752a33a1868b7a3ca631ea88049d53ee5d293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Cold preservation</topic><topic>Cold Temperature</topic><topic>Cryopreservation</topic><topic>Digestive system</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Ischemia-reperfusion injury</topic><topic>Ischemic Preconditioning</topic><topic>Liver - metabolism</topic><topic>Liver Transplantation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Oxidative Stress - physiology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reperfusion Injury - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sindram, David</creatorcontrib><creatorcontrib>Rüdiger, Hannes A</creatorcontrib><creatorcontrib>Upadhya, Aravinda G</creatorcontrib><creatorcontrib>Strasberg, Steven M</creatorcontrib><creatorcontrib>Clavien, Pierre-Alain</creatorcontrib><collection>Pascal-Francis</collection><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 hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sindram, David</au><au>Rüdiger, Hannes A</au><au>Upadhya, Aravinda G</au><au>Strasberg, Steven M</au><au>Clavien, Pierre-Alain</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ischemic preconditioning protects against cold ischemic injury through an oxidative stress dependent mechanism</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2002</date><risdate>2002</risdate><volume>36</volume><issue>1</issue><spage>78</spage><epage>84</epage><pages>78-84</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><coden>JOHEEC</coden><abstract>Background/Aims
: Ischemic injury in cold preserved livers is characterized by sinusoidal endothelial cell (SEC) detachment and matrix metalloproteinase activity. Upon reperfusion reversible ischemic injury becomes permanent with SEC rapidly undergoing apoptosis. Ischemic preconditioning prevents reperfusion injury after normothermic ischemia. We hypothesized that ischemic preconditioning, through an oxygen free radical burst, protects against injury during cold preservation and reperfusion.
Methods
: Ischemic preconditioning was achieved in rats by clamping blood supply to the left and median lobes for 10
min followed by 15
min of reperfusion prior to preservation in cold University of Wisconsin solution for 30
h. In a second set of experiments, rats were pretreated with
N
-acetyl-cysteine (NAC). SEC apoptosis upon reperfusion was assessed in an isolated perfused rat liver (IPRL) model.
Results
: SEC detachment and activities of matrix metalloproteinase were significantly reduced in preconditioned livers. A decrease of SEC apoptosis after 1
h of reperfusion in the IPRL was noted in preconditioned livers compared to controls. Pretreatment with NAC reversed the beneficial effects of ischemic preconditioning on SEC detachment and apoptosis.
Conclusions
: Ischemic preconditioning is an effective strategy to prevent injury during cold preservation and after reperfusion. The protective effect is possibly mediated by oxygen free radicals.</abstract><cop>Oxford</cop><pub>Elsevier B.V</pub><pmid>11804668</pmid><doi>10.1016/S0168-8278(01)00229-X</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Apoptosis Biological and medical sciences Cold preservation Cold Temperature Cryopreservation Digestive system Investigative techniques, diagnostic techniques (general aspects) Ischemia-reperfusion injury Ischemic Preconditioning Liver - metabolism Liver Transplantation Male Medical sciences Oxidative Stress - physiology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Rats Rats, Wistar Reperfusion Injury - metabolism |
title | Ischemic preconditioning protects against cold ischemic injury through an oxidative stress dependent mechanism |
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