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DOI: 10.1055/s-2002-35425
Foetal Lung Maturation in 11β-Hydroxysteroid Dehydrogenase Type 1 Knockout Mice
Publikationsverlauf
Received: 16 May 2002
Accepted after revision: 25 July 2002
Publikationsdatum:
19. November 2002 (online)
Abstract
Glucocorticoids (GCs) induce surfactant synthesis in the late foetal lung. Deficient GC action causes respiratory distress syndrome (RDS). 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) converts inert cortisone (11-dehydrocorticosterone in rodents) into active cortisol (corticosterone), thus amplifying intracellular GC action. Reduction or loss of pulmonary 11β-HSD1 activity in glycyrrhetinic acid-treated rats substantially impaired foetal lung maturation (Hundertmark et al., Horm Metab Res, this issue). To test these data, we investigated 11β-HSD1 activity and lung maturity in the late foetal lung using 11β-HSD1 knockout mice. Control foetal mice showed high 11β-HSD activity in the late foetal lung and levels of plasma 11-dehydrocorticosterone were high. Lungs from 11β-HSD1 -/- mice had lower surfactant protein-A (mRNA and protein) levels and significant depletion of lung surfactant according to both light and electron microscopy, and also had reduced amniotic fluid lecithin/sphingomyelin ratios. These results support the previous experiments with glycyrrhetinic acid and emphasize the importance of 11β-HSD1 in foetal lung maturation.
Key words
1.1.1.146 - 11β-Hydroxysteroid Dehydrogenase - EC - Lung Maturation - Pulmonary Surfactant - Knockout Mice
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PD Dr. S. Hundertmark
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