This study evaluated the effect of varying levels of tyrosine intake on the
estimation of phenylalanine hydroxylation. Healthy men were fed 1 g protei
n kg(-1) . d(-1) for a 2-day period. On the third day, subjects consumed a
formula diet containing 1 g protein kg(-1) . d(-1) hourly over 10 hours, an
d primed hourly oral doses of L-[N-15]phenylalanine and L-[3,3-H-2(2)]tyros
ine for the last 6 hours. Each subject was studied at 7 levels of tyrosine
intake (3.0, 4.5, 6.0, 7.5, 9.0, 10.5, and 12.0 mg . kg(-1) . d(-1)) at a c
onstant intake of phenylalanine (9 mg . kg(-1) . d(-1), 4.55 mu mol . kg(-1
) . h(-1)). Phenylalanine hydroxylation was estimated from the ratio of pla
sma amino acid isotope enrichment of [N-15]phenylalanine and [N-15]tyrosine
and the tyrosine flux estimated from [H-2(2)]tyrosine enrichment. Phenylal
anine and tyrosine fluxes showed no significant response to alterations In
the intake of tyrosine. Linear regression analysis showed a significant res
ponse such that the rate of phenylalanine hydroxylation decreased as tyrosi
ne intake increased (R-2 = .21; P = .003). The mean rates of phenylalanine
hydroxylation were 3.89 to 8.06 mu mol . kg(-1) . h(-1). Given model uncert
ainties, the apparent protein breakdown observed at tyrosine intake levels
less than 10.5 mg . kg(-1) . d(-1), and the significant differences observe
d between the present data and our prior data, we cannot estimate the tyros
ine requirement with any degree of certainty with the present hydroxylation
results. Copyright (C) 2000 by W.B. Saunders Company.