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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
Main Authors: Sindram, David, Rüdiger, Hannes A, Upadhya, Aravinda G, Strasberg, Steven M, Clavien, Pierre-Alain
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creator Sindram, David
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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
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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. 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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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