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Journal of Lipid Research, Vol 37, 783-789, Copyright © 1996 by Lipid Research, Inc.
AM Salva, BO Ibe, E Cliborn, G Reyes and JU Raj
The metabolism of platelet activating factor (PAF) by lungs of near- term
fetal and 5- to 9-day-old lambs was studied during normoxia and hypoxia at
37 degrees C in 30 mM Tris buffer. PAF synthesis was studied in lung
cytosol and membrane using 250 microM [3H]acetyl CoA, 40 microM lyso-PAF,
and 50 micrograms protein. PAF catabolism was studied in lung homogenate
(LH) using 50 microM [3H]alkyl-PAF. PAF was extracted and assayed by
thin-layer chromatography (TLC) and liquid scintillation spectrometry.
Levels of PAF synthesized (nmol/min per mg protein) by fetal lung membrane
versus cytosol were 1.35 +/- 0.07 versus 0.61 +/- 0.08, which were greater
than those by newborn which were 0.33 +/- 0.07 versus 0.17 +/- 0.03.
Hypoxia did not alter PAF synthesis by the lungs. PAF catabolism (nmol
lyso-PAF/min per mg protein) by fetal LH was 0.07 +/- 0.01, which increased
to 0.24 +/- 0.02 during normoxia. In newborn LH, the rate was 0.24 +/- 0.04
and increased to 0.33 +/- 0.01 during normoxia. PAF catabolism was higher
in newborn than in fetal LH. An increase in pO2 augmented PAF catabolism,
more in fetal than in newborn LH. Thus rate of PAF synthesis decreases from
fetus to newborn, but PAF catabolism increases from fetus to newborn. The
higher rate of PAF synthesis coupled with a low rate of PAF catabolism in
the hypoxic environment of fetal lungs may predispose the fetus to a high
PAF level, which may contribute to the high basal vasomotor tone in fetal
lungs. A fall in PAF level with oxygenation, due to increased PAF
catabolism, may facilitate the normal fall in pulmonary vascular resistance
at birth.
ARTICLES
Hypoxia attenuates metabolism of platelet activating factor by fetal and newborn lamb lungs
Department of Pediatrics, Harbor-UCLA Medical Center, Torrance 90502, USA.
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