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Difference between revisions of "De Rebiere 2011 Open Biochem J"

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{{Publication
{{Publication
|title=de Rebière de Pouyade G, Salciccia A, Ceusters J, Deby-Dupont G, Serteyn D, Mouithys-Mickalad A (2011) Production of free radicals and oxygen consumption by primary equine endothelial cells during anoxia-reoxygenation. Open Biochem J 5:52-59.
|title=de Rebière de Pouyade G, Salciccia A, Ceusters Justine D, Deby-Dupont G, Serteyn D, Mouithys-Mickalad A (2011) Production of free radicals and oxygen consumption by primary equine endothelial cells during anoxia-reoxygenation. Open Biochem J 5:52-59.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/22207886 PMID: 22207886]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/22207886 PMID: 22207886]
|authors=de Rebiere de Pouyade G, Salciccia A, Ceusters J, Deby-Dupont G, Serteyn D, Mouithys-Mickalad A
|authors=de Rebiere de Pouyade G, Salciccia A, Ceusters Justine D, Deby-Dupont G, Serteyn D, Mouithys-Mickalad A
|year=2011
|year=2011
|journal=Open Biochem J
|journal=Open Biochem J
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|tissues=Endothelial;epithelial;mesothelial cell
|tissues=Endothelial;epithelial;mesothelial cell
|preparations=Intact cells
|preparations=Intact cells
|injuries=Hypoxia, Oxidative stress;RONS
|injuries=Ischemia-reperfusion, Oxidative stress;RONS
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
}}
}}

Latest revision as of 13:31, 16 June 2015

Publications in the MiPMap
de Rebière de Pouyade G, Salciccia A, Ceusters Justine D, Deby-Dupont G, Serteyn D, Mouithys-Mickalad A (2011) Production of free radicals and oxygen consumption by primary equine endothelial cells during anoxia-reoxygenation. Open Biochem J 5:52-59.

» PMID: 22207886

de Rebiere de Pouyade G, Salciccia A, Ceusters Justine D, Deby-Dupont G, Serteyn D, Mouithys-Mickalad A (2011) Open Biochem J

Abstract: The endothelium plays an active role in ischemia/reperfusion injuries. Herein, we report the effect of a single or successive cycles of anoxia/reoxygenation (A/R) on the mitochondrial respiratory function of equine endothelial cells (cultured from carotids) monitored by high-resolution oxymetry, and on their production of reactive oxygen species (ROS). ROS were measured by electron paramagnetic resonance (ESR) using POBN and DMPO spin traps, and by gas chromatography (GC) of ethylene released by ROS-induced α-keto-γ-(methylthio)butyric acid (KMB) oxidation. The oxygen consumption significantly decreased with the number of A/R cycles, and POBN-ESR spectra were specific of adducts formed in the cells from superoxide anion. After a one-hour A/R cycle, high intensity DMPO-ESR spectra were observed and assigned to superoxide anion trapping; the GC results confirmed an important production of ROS compared to normoxic cells. These results show that A/R induces mitochondrial alterations in endothelial cells, and strongly stimulates their oxidative activity as demonstrated by ESR and GC methods.


O2k-Network Lab: BE Liege Votion DM


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Stress:Ischemia-reperfusion, Oxidative stress;RONS  Organism: Horse  Tissue;cell: Endothelial;epithelial;mesothelial cell  Preparation: Intact cells 



HRR: Oxygraph-2k