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Pharmacol Res ; 53(4): 372-9, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16504535

ABSTRACT

There is very little evidence on the value of giving corticoids in cases of seawater drowning induced acute lung injury/acute respiratory distress syndrome (ALI/ARDS). Therefore, this study aimed to investigate whether dexamethasone treatment can attenuate seawater instillation-induced acute lung injury in rabbits. Seawater (4 ml/kg body weight) was instilled into the lower trachea of ventilated, anesthetized rabbits. Then these rabbits were assigned randomly 20 min later to receive intravenous injection of 1mg/kg body weight of dexamethasone (dissolving in 2 ml of normal saline) or 2 ml of normal saline. All animals demonstrated immediate drops in arterial oxygen tension (PaO2) and the total thoracic compliance, which were significantly improved after 2 h of dexamethasone treatment. Histopathological study also indicated that dexamethasone treatment markedly attenuated lung histopathological changes, alveolar hemorrhage and inflammatory cells infiltration with evidence of decreasing of myeloperoxidase (MPO) activity and tumor necrosis factor-alpha (TNF-alpha) concentration in lung tissue. In addition, dexamethasone treatment reduced extravascular lung water and lung epithelial-endothelial barrier permeability, up-regulated the expression of surfactant protein-A (SP-A) and alpha-epithelial Na+ channel, and increased Na+/K+-adenosine triphosphatase (Na+/K+-ATPase) activity and Na+/K+-ATPase-alpha1 protein abundance. Thus, these data indicate that dexamethasone treatment might be of benefit in patients with seawater aspiration-induced ALI.


Subject(s)
Dexamethasone/pharmacology , Respiratory Distress Syndrome/drug therapy , Respiratory Distress Syndrome/metabolism , Sodium Channels/biosynthesis , Sodium-Potassium-Exchanging ATPase/biosynthesis , Animals , Epithelial Sodium Channels , Extravascular Lung Water/drug effects , Lung/drug effects , Lung/metabolism , Lung/pathology , Male , Oxygen/blood , Pulmonary Alveoli/drug effects , Pulmonary Alveoli/metabolism , Pulmonary Alveoli/pathology , Pulmonary Surfactant-Associated Protein A/biosynthesis , Pulmonary Surfactant-Associated Protein A/genetics , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Rabbits , Random Allocation , Respiratory Distress Syndrome/etiology , Respiratory Distress Syndrome/pathology , Seawater , Sodium Channels/genetics , Sodium-Potassium-Exchanging ATPase/genetics , Up-Regulation/drug effects
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