During decreased fetal glucose delivery, endogenous substrates increas
ingly support metabolic rate. If oxidation of fetal amino acid stores
(i.e. protein) is to provide such substrate. either protein synthesis
must decrease or protein breakdown must increase. Both of these change
s would diminish fetal protein accretion, an important component of fe
tal growth. This study was performed, therefore, to find if decreased
glucose delivery alters fetal leucine metabolism. Catheters were place
d in six sheep fetuses under maternal general anesthesia, and, after 6
days recovery, fetal leucine metabolism was measured by infusion of [
1 - C-14]leucine before and after fetal glucose delivery was decreased
by infusing insulin to the ewe. Later (2 days) the experiment was rep
eated in reverse order. Decreased fetal glucose delivery was associate
d with a 19% decrease in the rate of fetal leucine disposal (P < 0.001
), a 42% decrease in the rate of exogenous leucine uptake (P < 0.01),
and no change in the rate of fetal leucine decarboxylation. The use of
leucine for protein synthesis by the fetus fell by 23% (P < 0.001), w
hereas the rate of protein breakdown did not change. Consequently, dur
ing decreased fetal glucose delivery, leucine accretion into fetal pro
teins was 28% (P < 0.02) of the control rate. In summary, fetal oxidat
ion of amino acids derived from increased protein breakdown is not the
source of endogenous substrate needed by the fetus with restricted gl
ucose availability. Fetal protein synthesis did decrease, however, dim
inishing the accretion of leucine into protein.