H. Asano et al., TISSUE DNA-SYNTHESIS IN THE PRETERM OVINE FETUS FOLLOWING 8 HOURS OF SUSTAINED HYPOXEMIA, Journal of the Society for Gynecologic Investigation, 4(5), 1997, pp. 236-240
OBJECTIVE: Protein synthesis is significantly decreased in the near-te
rm ovine fetus in response to induced hypoxemia of several hours' dura
tion. We therefore sought to determine the extent to which DNA synthes
is rates as an index of tissue mitotic activity are also affected by s
imilarly induced compromises in fetal oxygenation. METHODS: Fetal shee
p were studied at 0.75 of gestation during a normoxic control period a
nd an 8-hour experimental period of either sustained hypoxemia induced
by lowering maternal inspired oxygen concentration of 11-8% (hypoxia
group, n = 7) or continued exposure to room air (control group, n = 5)
. To estimate DNA synthesis rate, [H-3]-thymidine (1 Mci/kg) was injec
ted intravenously into each fetus at the beginning of the experimental
period. RESULTS: Sustained hypoxemia with a reduction in fetal arteri
al O-2 content from (mean +/- standard error of the mean) 4.3 +/- 0.1
to 1.5 +/- 0.1 mmol/L by the end of study resulted in a variable degre
e of fetal acidemia, 7.26 +/- 0.03 (range from 7.41 to 7.10), which wa
s entirely metabolic in nature. CONCLUSION: The DNA synthesis rates of
most tissues were not significantly changed by the 8 hours of sustain
ed hypoxemia, suggesting that restrictions in protein synthesis in res
ponse to fetal hypoxia are initially due to a differential effect on n
onmitotic synthetic processes at this stage of development. However, s
elective decreases in the DNA synthesis rates of the hippocampus (appr
oximately 50%, P < .01), adrenals (approximately 48%, P < .05), and le
ft and right myocardial ventricles (approximately 42% and 27%, respect
ively, P = .08) were evident which may reflect altered mitotic activit
y in response to tissue related changes in energy expenditure. Copyrig
ht (C) 1997 by the Society for Gynecologic Investigation.