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<dc:title xml:lang="fr">Intérêt des microparticules pour l'étude de l'ischémie reperfusion en tranplantation pulmonaire basé sur un modèle de perfusion ventilation pulmonaire ex vivo chez le rat</dc:title>
<dcterms:alternative xml:lang="en">Relevance of microparticles for the study of ischemia reperfusion in lung transplantation using an experimental model of ex vivo rat lung reperfusion and ventilation</dcterms:alternative>
<dc:subject xml:lang="fr">Ischémie reperfusion</dc:subject>
<dc:subject xml:lang="fr">Reperfusion ex vivo</dc:subject>
<dc:subject xml:lang="fr">Microparticules</dc:subject>
<dc:subject xml:lang="en">Ischemia reperfusion</dc:subject>
<dc:subject xml:lang="en">Ex vivo reperfusion</dc:subject>
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<tef:elementdEntree autoriteExterne="028120035" autoriteSource="Sudoc">Réaction du greffon contre l'hôte</tef:elementdEntree>
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<tef:elementdEntree autoriteExterne="201300257" autoriteSource="Sudoc">Lésions d'ischémie-reperfusion</tef:elementdEntree>
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<dcterms:abstract xml:lang="fr">L’ischémie reperfusion pulmonaire et sa traduction clinique la dysfonction primaire du greffon sont responsables d’une morbi-mortalité importante en transplantation pulmonaire aussi bien à court terme qu’à long terme. Nous avons voulu faire la démonstration de la pertinence des microparticules comme marqueur de l’ischémie reperfusion pulmonaire. Nous avons reproduit et validé la stabilité d’un modèle de perfusion ventilation ex vivo de poumon de rat aussi bien en conditions normales (pas d’ischémie pulmonaire avant reperfusion) qu’en conditions extrêmes (1 h d’ischémie chaude avant reperfusion pulmonaire). Nous avons étudié la génération de microparticules par des poumons soumis à des conditions variables d’ischémie froide et d’ischémie chaude. Les poumons soumis à de fortes conditions d’ischémie froide (20h) produisent un pic précoce de microparticules d’origine épithéliale alvéolaire, leucocytaire et endothéliale. Nous en concluons que le modèle de perfusion ventilation ex vivo de poumons de rats est un modèle pertinent pour l’étude des réactions d’ischémie reperfusion. Les microparticules apparaissent comme un marqueur précoce des lésions d’ischémie reperfusion pulmonaires dans ce modèle.</dcterms:abstract>
<dcterms:abstract xml:lang="en">Lung ischemia reperfusion and its clinical expression as primary graft dysfunction are provider of immediate and long term morbidity and mortality for patients. We aimed at demonstrating the usefulness and relevance of microparticles as biomarkers for lung ischemia reperfusion injury. We first reproduced an ex vivo rat lung perfusion and ventilation experimental model. Stability of the model was validated for normal conditions (no ischemia before reperfusion) as well as for extreme conditions (1 hour warm ischemia before reperfusion). The generation of microparticles was studied in that model for variable conditions of cold ischemia and for warm ischemia. Lung submitted to strong ischemic injury (20hours cold ischemia) generate an early pike of microparticles originated from leukocyes, endothelial cells, and epithelial alveolar cells. We may conclude the ex vivo model of rat lung perfusion and ventilation is relevant for the study of lung ischemia reperfusion injury. Microparticles are relevant markers of rat lung ischemia reperfusion injury in our model.</dcterms:abstract>
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