Mg. Davey et al., Stimulation of lung growth in fetuses with lung hypoplasia leads to altered postnatal lung structure in sheep, PEDIAT PULM, 32(4), 2001, pp. 267-276
Increased lung expansion in the fetus stimulates lung growth and is being t
rialed clinically to reverse severe fetal lung hypoplasia. Our aim was to e
xamine the effects of increased fetal lung expansion in the presence of lun
g hypoplasia on lung structure in sheep at term and 8 weeks after birth. Lu
ng hypoplasia was induced in 15 fetal sheep by continuous drainage of trach
eal fluid, commencing at similar to 113 days of gestation (term, similar to
148 days). In 10 of these fetuses, tracheal obstruction (TO) was performed
from 137-147 days of gestation (treated lung hypoplasia, TLH), while lung
liquid drainage continued until term in the remaining 5 fetuses (untreated
lung hypoplasia, ULH). Lung tissues were obtained from 5 TLH, 5 ULH, and 5
control lambs at birth, and from 5 TLH and 5 control lambs at 8 weeks after
birth.
At birth, alveolar number, surface area, and interalveolar wall thickness w
ere not different between TLH and control lambs, whereas airspace diameter
was greater in TLH lambs (72.7 +/- 3.0 mum) than in controls (58.4 +/- 4.3
mum). Diameters of airspaces were not different between ULH and control lam
bs; however, alveolar numbers and surface area were reduced, while interalv
eolar wall thickness was increased in ULH lambs compared to controls. At 8
weeks after birth, alveolar number (928.0 +/- 66.1 x 10(6)) and surface are
a (30.3 +/- 2.2 m(2)) in TLH lambs were lower, whereas interalveolar wall t
hickness (83.0 +/- 3.1 mum) was greater than in control lambs (2,263.6 +/-
261.6 x 10(6), 46.7 +/- 4.8 m(2), and 68.6 +/- 2.1 mum, respectively).
Our data show that TO restores most aspects of lung structure to normal in
fetuses with lung hypoplasia but leads to altered alveolar development. The
presence of fewer, larger alveoli in postnatal TLH animals may predispose
these animals to respiratory complications during later life. (C) 2001 Wile
y-Liss, Inc.