OVINE FETAL PROTEIN-METABOLISM DURING DECREASED GLUCOSE DELIVERY

Authors
Citation
Jr. Milley, OVINE FETAL PROTEIN-METABOLISM DURING DECREASED GLUCOSE DELIVERY, The American journal of physiology, 265(4), 1993, pp. 50000525-50000531
Citations number
30
Categorie Soggetti
Physiology
ISSN journal
00029513
Volume
265
Issue
4
Year of publication
1993
Part
1
Pages
50000525 - 50000531
Database
ISI
SICI code
0002-9513(1993)265:4<50000525:OFPDDG>2.0.ZU;2-3
Abstract
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.