24-HOUR INTRAVENOUS AND ORAL TRACER STUDIES WITH L-[1-C-13]-2-AMINOADIPIC ACID AND L-[1-C-13]LYSINE AS TRACERS AT GENEROUS NITROGEN AND LYSINE INTAKES IN HEALTHY-ADULTS
Ae. Elkhoury et al., 24-HOUR INTRAVENOUS AND ORAL TRACER STUDIES WITH L-[1-C-13]-2-AMINOADIPIC ACID AND L-[1-C-13]LYSINE AS TRACERS AT GENEROUS NITROGEN AND LYSINE INTAKES IN HEALTHY-ADULTS, The American journal of clinical nutrition, 68(4), 1998, pp. 827-839
Background: This is a continuation of investigations of the relations
between amino acid kinetics and amino acid dietary requirements in hea
lthy adults. Objective: The aim was to investigate the 24-h pattern an
d rate of the metabolism of an L-[1-C-13]-2-aminoadipic acid ([C-13]AA
A) tracer and of whole-body L-[1-C-13]lysine ([C-13]lysine) oxidation
and balance in healthy, young adults receiving a generous intake of ly
sine. Design: Thirteen healthy adults were given an adequate, L-amino
acid-based diet supplying 77 mg lysine.kg(-1).d(-1) for 6 d before the
tracer studies. Two subjects received [C-13]AAA intravenously and 2 r
eceived it orally; 3 subjects received [C-13]lysine intravenously and
6 received it orally. We measured (CO2)-C-13 output, plasma [C-13]AAA
and [C-13]lysine enrichment, and urinary [C-13]AAA. Results: [C-13]AAA
oxidation was estimated to be higher after the orally administered th
an after the intravenously administer tracer; plasma [C-13]AAA was sim
ilar to urinary [C-13]AAA. Whole-body lysine oxidation showed a rhythm
that was induced by meal feeding. The intravenous [C-13]lysine tracer
gave mean estimates of lysine balances (lysine intake minus oxidation
) that apparently were too low (-15.7 mg.kg(-1).d(-1)) or too high (16
.6 mg.kg(-1).d(-1), P < 0.05 from zero balance) on the basis of urinar
y [C-13]AAA or plasma [C-13]lysine estimates of oxidation, respectivel
y. For the orally administered tracer and plasma [C-13]lysine enrichme
nt, the mean balance was slightly positive (8.7 mg.kg(-1).d(-1), P < 0
.05 from zero). Conclusions: Use of urinary [C-13]AAA as an index of t
he enrichment of the precursor pool did not appear to significantly im
prove the estimate of the fasting and feeding components of daily lysi
ne balance. For estimates of daily, whole-body lysine oxidation, we pr
opose use of plasma [C-13]lysine with a 24-h, orally administered trac
er protocol.