C. Plath et al., N-15-TRACER STUDIES IN FORMULA-FED PRETERM INFANTS - THE ROLE OF GLYCINE SUPPLY IN PROTEIN-TURNOVER, Journal of pediatric gastroenterology and nutrition, 23(3), 1996, pp. 287-297
In preterm infants, protein-turnover rates obtained by [N-15]glycine a
s a tracer are known to be overestimated. This may reflect the insuffi
cient supply of dietary glycine. In this randomized study, the influen
ce of a glycine-rich diet on whole body protein turnover rates in eigh
t male preterm infants (29-32 weeks, 1,200-2,540 g birthweight) using
the N-15-tracer technique on days 21 and 28 of life was investigated t
o evaluate the necessity of supplementing preterm infant formulas with
proteins rich in glycine. Before and during the study, the infants we
re alternately fed with a commercial available preterm infant formula
(I, 2% protein, 40 mg glycine/dl) and a variety of this formulation wi
th glycine-rich proteins (II, 2% protein, 130 mg glycine/dl). The prot
ein-turnover rates were computed after N-15-single-pulse labeling with
the help of the three-compartment model (TCM) and the urinary ammonia
end-product method (AEPM). The tracer used was [N-15]glycine (dosage:
2 mg N-15/kg). For the determination of N-15-excess-excretion kinetic
s, fractionated urine specimens were collected over a 36-h period. The
protein-turnover rate calculated by TCM was 8.8 +/- 1.6 g/kg/day (for
mula I) and 7.7 +/- 2.0 g/kg/day (formula II); using AEPM, the rate wa
s 8.7 +/- 2.5 g/kg/day and 7.5 +/- 1.5 g/kg/day, respectively. We conc
lude that the presaturation of the precursor pool by an adequate glyci
ne intake minimizes drawbacks that may arise when using [N-15]glycine
as a tracer in preterm infants, and a protein concentration of 2%, as
in formula I, and consequently, a 170% glycine content when compared w
ith the same human milk volume, meets the glycine requirement.