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Pulm Pharmacol Ther ; 36: 31-6, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26704083

RESUMO

INTRODUCTION: Secretory phospholipase A2 regulates surfactant catabolism and inflammatory cascade. This enzyme is correlated with compliance, oxygenation and major outcomes in various forms of acute respiratory failure. Steroids inhibit secretory phospholipase A2 in cell culture and are widely used to boost surfactant production before preterm delivery. No data are available about the effect of antenatal steroids on secretory phospholipase A2 in the offspring: we aimed to study this effect in a rat model of preterm lung. MATERIAL AND METHODS: Fifteen pregnant Wistar rats were randomized to receive betamethasone, dexamethasone or placebo at 20 and 21 days gestation. Newborn rats were supported for 8 h and then sacrificed: lung tissue was analysed for secretory phospholipase A2 expression and activity, inflammatory mediators and protein content. Lipidomics was analysed using liquid chromatography-mass spectrometry. RESULTS: Secretory phospholipase A2 expression was significantly reduced by antenatal steroids (p < 0.001). Secretory phospholipase A2 activity, TNFα and lysophosphatidylethanolamine, a product of phospholipase reaction, were lowest in betamethasone-treated rats (p < 0.001). There was a strong correlation between secretory phospholipase A2 activity and lysophosphatidylethanolamine (r = 0.75; p = 0.001) and this remained significant after adjustment for total proteins or phospholipids. CONCLUSIONS: Antenatal steroids decrease secretory phospholipase A2 in rat model of preterm lung.


Assuntos
Pulmão/enzimologia , Fosfolipases A2 Secretórias/antagonistas & inibidores , Nascimento Prematuro/patologia , Esteroides/farmacologia , Animais , Animais Recém-Nascidos , Anti-Inflamatórios/farmacologia , Betametasona/farmacologia , Dexametasona/farmacologia , Feminino , Mediadores da Inflamação/metabolismo , Metabolismo dos Lipídeos/efeitos dos fármacos , Pulmão/patologia , Lisofosfolipídeos/metabolismo , Gravidez , Surfactantes Pulmonares/metabolismo , Ratos , Ratos Wistar , Fator de Necrose Tumoral alfa/metabolismo
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