American Journal of Respiratory and Critical Care Medicine · 2003 · 45 citations · 47 references
MedicinePharmacologyPhysiologyIon Channel BiophysicsMolecular PharmacologyTransplant SurgeryAcute Lung InjuryLung TransplantationPulmonary PhysiologyTransplant PharmacologyEdema FormationEpithelial Sodium ChannelsPulmonary CirculationSodium Channel PhysiologySodium-potassium Adenosine TriphosphataseSodium-potassium AtpaseSodium-potassium-atpase RegulationTransport In Lung Tissue
To determine the impact of transplantation-associated injury on the clearance mechanisms of pulmonary edema, we created a canine single lung transplant model. After 3 hours of preservation and 4 hours of reperfusion, right native lungs and left transplanted lungs were used to measure alveolar liquid clearance (ALC) in ex vivo liquid-filled lung preparations. We also examined the role of the pulmonary circulation in edema clearance in in vivo liquid-filled lungs between 4 and 8 hours of reperfusion. To study molecular modifications in ALC, we also measured expression levels of the epithelial sodium channel (ENaC) and sodium-potassium-adenosine triphosphatase (ATPase). We found that ALC was significantly lower in transplanted than in right native lungs ex vivo (p < 0.05) and that transplanted lungs did not respond to the beta-adrenergic agonist terbutaline. Our in vivo study confirmed the ex vivo results. Molecular analyses revealed that ENaC messenger RNA but not sodium-potassium-ATPase was significantly decreased in transplanted lungs (p < 0.01). Furthermore, there was a significant decrease in ENaC protein expression. Therefore, we conclude that the current investigation indicates that the lung injury caused by lung preservation and transplantation significantly reduces the edema clearance ability of transplanted lungs.
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