To investigate the role of insulin-like growth factor I (IGF-I) in the regulation of fetal metabolism, the kinetics of leucine, phenylalanine, and glucose were assessed in the chronically catheterized ovine fetus (0.85 gestation) before and during infusion of recombinant human IGF-I (rhIGF-I). Substrate kinetics were determined by tracer dilution. rhIGF-I was infused at 6.7 nmol · kg fetus-1 h-1. Fetal insulin and growth hormone concentrations were significantly decreased by 50% during rhIGF-I infusion. Net umbilical glucose uptake was unchanged, and glucose rate of appearance increased in the fed state only. There were no changes in the net umbilical uptakes of leucine or phenylalanine, but the rates of appearance of both declined during rhIGF-I infusion, indicative of decreased fetal protein breakdown (R(a,Leu) 45.4 ± 1.40 to 40 ± 1.4 μmol/min in the fed state, 43 ± 1.5 to 37 ± 1.5 μmol/min in the fasted state; R(a,Phe) 10.7 ± 0.3 to 10.4 ± 0.3 μmol/min in the fed state and from 10.7 ± 0.3 to 9.8 ± 0.3 μmol/min in the fasted state). Leucine oxidation was also decreased (8.90 ± 0.76 to 6.52 ± 0.81 μmol/min, P = 0.025), more so in the fasted than the fed state. These results indicate a significant antiproteolytic endocrine effect for IGF-I in the late-gestation mammalian fetus.
|Original language||English (US)|
|Journal||American Journal of Physiology - Endocrinology and Metabolism|
|Issue number||1 34-1|
|State||Published - Jul 1996|
- growth hormone
- insulin-like growth factor I
ASJC Scopus subject areas