Maternal Betamethasone and Chorioamnionitis Induce Different Collagenases during Lung Maturation in Fetal SheepSweet D.G. · Huggett M.T. · Warner J.A. · Moss T.J.M. · Kloosterboer N. · Halliday H.L. · Newnham J.P. · Kallapur S.G. · Jobe A.H. · Kramer B.W.
aDepartment of Child Health, The Queen’s University of Belfast, bSchool of Biological Sciences, University of Southampton, UK; cSchool of Women’s and Infants’ Health, University of Western Australia, Perth, W.A., Australia; dDivision of Pulmonary Biology, University of Cincinnati Medical Centre, Cincinnati, Ohio, USA; eDepartment of Pediatrics, University Hospital Maastricht, Maastricht, The Netherlands
Background: Fetal lung maturation occurs after both maternal corticosteroid administration and chorioamnionitis. The effectors of this antenatally-induced lung maturation are not understood. Matrix metalloproteinases (MMPs) 2 and 9 are type-IV collagenases that can degrade alveolar basement membranes. Objectives: We hypothesized that the structural changes of lung maturation by both antenatal corticosteroid treatment and chorioamnionitis would be associated with increases in these MMPs. Methods: 64 pregnant ewes were randomly assigned to one of four treatment groups: intra-amniotic injection of 10 mg endotoxin, maternal intramuscular injection of 0.5 mg/kg betamethasone, both treatments combined or saline-treated controls. We quantified MMP-2 which is derived from connective tissue and MMP-9 which is predominantly derived from neutrophils in fetal lung fluid of lambs after maternal corticosteroid therapy and induction of chorioamnionitis and the combination of both therapies given at 109–111 days’ gestational age with delivery 1, 5 or 15 days later. Results: Betamethasone, endotoxin and the combined treatments increased both surfactant pool size, lung gas volume and reduced alveolar wall thickness at 15 days. MMP-2 concentration was increased after betamethasone. MMP-9 concentration increased after endotoxin-induced chorioamnionitis but decreased by the combined treatments. Conclusion: Lung maturation via different pathways may use different forms of collagenases for remodelling lung structure.
Boris W. Kramer, MD, PhD
Department of Pediatrics, Academisch Ziekenhuis Maastricht
NL–6202 AZ Maastricht (The Netherlands)
Tel. +31 43 387 4202, Fax +31 43 387 5246, E-Mail firstname.lastname@example.org
Supported by HL-K08 70711 and HL-65397 from the National Institute of Health.
Received: August 22, 2007
Accepted after revision: October 29, 2007
Published online: February 11, 2008
Number of Print Pages : 8
Number of Figures : 5, Number of Tables : 0, Number of References : 37
Neonatology (Fetal and Neonatal Research)
Vol. 94, No. 2, Year 2008 (Cover Date: August 2008)
Journal Editor: Halliday, H.L. (Belfast), Speer, C.P. (Würzburg)
ISSN: 1661–7800 (Print), eISSN: 1661–7819 (Online)
For additional information: http://www.karger.com/NEO