N. Lefloch et al., IN-VIVO THREONINE OXIDATION IN GROWING PIGS FED ON DIETS WITH GRADED-LEVELS OF THREONINE, British Journal of Nutrition, 75(6), 1996, pp. 825-837
Threonine oxidation to glycine was investigated in vivo in twelve grow
ing pigs (27.4 kg live weight) fed on one of the following three diets
with graded levels of threonine supply: a low-threonine diet (LT), a
control well-balanced diet (C) or a high-threonine diet (HT), during 1
0 h constant infusion of L-[1-C-13]threonine and [2-H-3]glycine in the
cranial vena cava and [1-C-14]glycine in the portal vein, C-13-threon
ine and glycine enrichments and [H-3]glycine and [C-14]glycine specifi
c radioactivities (SR) were determined at plateau in peripheral venous
plasma, liver and pancreas, Glycine production rates calculated from
plasma [2-H-3]glycine or [1-C-14]glycine SR gave similar values sugges
ting that [1-C-14]glycine SR could be used in order to estimate whole-
body glycine flux. The high pancreas [1-C-13]glycine enrichment provid
ed evidence that the pancreas may be, with the Liver, a major site of
threonine oxidation to glycine, Moreover, the present findings suggest
that threonine transport into the liver could be the limiting step of
threonine oxidation in this tissue when dietary threonine supply is l
ow, Total threonine oxidation to glycine, calculated from plasma value
s of enrichment and specific radioactivity, was low and constant when
the estimated absorbed threonine was lower than 4 g/d and increased fo
r higher amounts of absorbed threonine.