Intravenous dexamethasone attenuated inflammation and influenced apoptosis of lung cells in an experimental model of acute lung injury
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
28006948
DOI
10.33549/physiolres.933531
PII: 933531
Knihovny.cz E-zdroje
- MeSH
- akutní poškození plic farmakoterapie metabolismus patologie MeSH
- antiflogistika aplikace a dávkování MeSH
- apoptóza účinky léků fyziologie MeSH
- bronchoalveolární lavážní tekutina cytologie MeSH
- dexamethason aplikace a dávkování MeSH
- intravenózní infuze MeSH
- králíci MeSH
- mediátory zánětu antagonisté a inhibitory metabolismus MeSH
- modely nemocí na zvířatech * MeSH
- neutrofily účinky léků metabolismus MeSH
- plíce cytologie účinky léků metabolismus MeSH
- zvířata MeSH
- Check Tag
- králíci MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antiflogistika MeSH
- dexamethason MeSH
- mediátory zánětu MeSH
Acute lung injury (ALI) is characterized by diffuse alveolar damage, inflammation, and transmigration and activation of inflammatory cells. This study evaluated if intravenous dexamethasone can influence lung inflammation and apoptosis in lavage-induced ALI. ALI was induced in rabbits by repetitive saline lung lavage (30 ml/kg, 9+/-3-times). Animals were divided into 3 groups: ALI without therapy (ALI), ALI treated with dexamethasone i.v. (0.5 mg/kg, Dexamed; ALI+DEX), and healthy non-ventilated controls (Control). After following 5 h of ventilation, ALI animals were overdosed by anesthetics. Total and differential counts of cells in bronchoalveolar lavage fluid (BAL) were estimated. Lung edema was expressed as wet/dry weight ratio. Concentrations of IL-1beta, IL-8, esRAGE, S1PR3 in the lung were analyzed by ELISA methods. In right lung, apoptotic cells were evaluated by TUNEL assay and caspase-3 immunohistochemically. Dexamethasone showed a trend to improve lung functions and histopathological changes, reduced leak of neutrophils (P<0.001) into the lung, decreased concentrations of pro-inflammatory IL-1beta (P<0.05) and marker of lung injury esRAGE (P<0.05), lung edema formation (P<0.05), and lung apoptotic index (P<0.01), but increased immunoreactivity of caspase-3 in the lung (P<0.001). Considering the action of dexamethasone on respiratory parameters and lung injury, the results indicate potential of this therapy in ALI.
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