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American Journal of Clinical Nutrition, Vol. 73, No. 2, 276-282, February 2001
© 2001 American Society for Clinical Nutrition

Original Research Communication

Tyrosine requirement of healthy men receiving a fixed phenylalanine intake determined by using indicator amino acid oxidation1,2,3,4

Susan A Roberts, Jane M Thorpe, Ronald O Ball and Paul B Pencharz

1 From the Departments of Nutritional Sciences and Paediatrics, University of Toronto; The Research Institute, The Hospital for Sick Children, Toronto; and the Department of Agricultural, Food and Nutritional Sciences, University of Alberta, Edmonton, Canada.

2 Presented in part at Experimental Biology '98, April 18–22, 1998 [FASEB J 1998;12:A860 (abstr)].

3 Supported by grant MT 10321 from the Medical Research Council of Canada. Mead Johnson Canada provided the protein-free powder. SAR received partial support from the Fonds pour la Formation de Chercheurs a l'Aide a la Recherche, an Ontario Graduate Scholarship, and The University of Toronto.

4 Address reprint requests to PB Pencharz, Division of Gastroenterology and Nutrition, The Hospital for Sick Children, 555 University Avenue, Toronto, Canada M5G 1X8. E-mail: paul.pencharz{at}sickkids.on.ca.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Background: The currently accepted total aromatic amino acid requirement for adults is based on nitrogen balance measurements in individuals who received their intake of aromatic amino acids solely as phenylalanine.

Objective: The objective of this study was to determine the requirement for the amino acid tyrosine in healthy men receiving an adequate, but not excessive, intake of phenylalanine (9 mg•kg-1•d-1).

Design: The effect of a graded intake of tyrosine was determined in 6 healthy men consuming energy-sufficient diets containing 1 g protein•kg-1•d-1. The tyrosine requirement was determined by using indicator amino acid oxidation methodology with L-[1-13C]lysine as the indicator. Subjects were studied at each of 7 tyrosine intakes.

Results: A graded intake of tyrosine had no effect on lysine flux. The mean tyrosine requirement was determined from the response of the oxidation of L-[1-13C]lysine to breath 13CO2. A 2-phase linear regression crossover analysis of breath 13CO2 identified the breakpoint and upper 95% confidence limit, which represents the mean and safe intakes, to be 6.0 and 7.0 mg•kg-1•d-1, respectively.

Conclusions: The safe intake of total aromatic amino acids calculated from the present results for tyrosine and our previous estimate for phenylalanine is estimated to be 21 mg•kg-1•d-1. This intake is 1.5 times the currently recommended total aromatic amino acid intake of the FAO/WHO/UNU (1985), 14 mg•kg-1•d-1. Furthermore, the absolute aromatic amino acid requirement may be dependent on the proportional balance of these amino acids in the diet.

Key Words: Amino acid metabolism • aromatic amino acids • stable isotopes • adult amino acid requirements • phenylalanine • tyrosine • men


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
In the past decade there has been a resurgence of interest in aromatic amino acid requirements (1–9). These studies focused largely on the phenylalanine requirement in persons consuming a diet either lacking or low in tyrosine (2–4, 8). From the results of these studies, a total aromatic amino acid requirement was estimated; however, it was assumed that phenylalanine can provide the entire tyrosine requirement as well as can a balanced intake of phenylalanine and tyrosine.

To our knowledge, the study by Zello et al (1) is the only investigation in adult humans that examined the body's minimum phenylalanine requirement under conditions of excess tyrosine intake. In the presence of excess tyrosine, a phenylalanine intake above that required is believed to be preferentially oxidized before first equilibrating with the whole-body tyrosine pool (10, 11). Zello et al's design isolated the component of phenylalanine requirement from that of total aromatic amino acids. The estimated mean requirement and safe (upper 95% confidence limit) phenylalanine intake derived from this study were 9.1 and 14 mg•kg-1•d-1, respectively.

Tyrosine is a conditionally indispensable amino acid. Although it is indispensable in neonates (12), it is a dispensable amino acid in healthy adults because it can be synthesized through hepatic phenylalanine hydroxylation (13) when sufficient phenylalanine is provided in the diet. However, in conditions known to impair aromatic amino acid metabolism, such as hepatic and renal disease, a preformed balanced source of the amino acid may be required to minimize aromatic amino acid excess and catabolism.

The goal of this study was to estimate, for the first time, tyrosine requirements in adults at fixed and adequate, but not excessive, phenylalanine intakes. An indicator amino acid oxidation technique was used, with L-[1-13C]lysine as the indicator. This study was the first to use the indicator amino acid oxidation technique to determine the requirements of a dispensable amino acid. In addition, this study was the first to use lysine as an indicator of amino acid requirements in adult humans; we previously used lysine as an indicator to determine tyrosine requirements in children with phenylketonuria (9). In addition to estimating the tyrosine requirement, we used our previous estimated minimum phenylalanine requirement (1) to provide an estimate of total aromatic amino acid requirements.


   SUBJECTS AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Subjects
Six healthy men with a mean (±SD) age of 29 ± 9 y were enrolled in the study. Subjects participated in the study as outpatients; all studies were carried out in the Clinical Investigation Unit at The Hospital for Sick Children, Toronto. Subjects were excluded from the study if they had a chronic disease, had a history of weight loss, had an endocrine disorder, or were receiving drug therapy. The purpose of the study and the potential risks associated with the protocol were explained in detail to the subjects. Participants were encouraged to maintain their usual physical activities throughout the study period. Written, informed consent was obtained from all subjects. The study protocol was approved by both the University of Toronto Human Experimentation Committee and the Human Review Committee of The Hospital for Sick Children. All volunteers were remunerated for their participation. Subject characteristics are summarized in Table 1Go.


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  		TABLE 1. Individual characteristics and energy intakes of healthy men
 
Experimental design and dietary intake
In our earlier study (1) we established a mean phenylalanine requirement of 9.1 mg•kg-1•d-1 and an upper 95% CI of 14 mg•kg-1•d-1 under conditions of excess tyrosine intake (40 mg•kg-1•d-1). In the present study we chose to use a fixed phenylalanine intake of 9.0 mg•kg-1•d-1, which approximates the average minimal phenylalanine requirement (1). We reasoned that although a lower or a higher phenylalanine intake would alter the estimate of tyrosine needs, the average phenylalanine intake should allow extrapolation of the data to an estimate of total aromatic amino acid requirements.

Each subject was allocated to receive each of 7 different tyrosine intakes in random order. Studies were separated by >=1 wk and all studies were carried out within 3 mo. For 2 d before each study day, subjects consumed a controlled formula that provided adequate energy and protein intakes. The basal metabolic rate was determined first by using predictive equations for each subject (14). The basal metabolic rate for each subjects was multiplied by 1.7 to determine total daily energy needs and hence the amount of energy to provide the subjects. Protein was provided at an intake of 1 g•kg-1•d-1. The formula was a low-protein milk shake (Scandishake; Scandipharm, Inc, Birmingham, AL) prepared with skim milk and added carbohydrate (Caloreen; Baxter Corporation, Mississauga, Canada) and protein (Promod; Ross Laboratories, Columbus, OH) to tailor the formula to the exact energy and protein intakes required. The diet was given as 4 meals spread throughout the day. Except for water, no additional food or beverages were consumed.

Starting at 0600 on the study day, subjects consumed the same protein and energy intakes in the form of a liquid formula and protein-free cookies (15). Meals were provided hourly for 12 h, each meal providing one-twelfth of the daily requirement. The diet provided 37% of energy as fat, 53% as carbohydrate, and 10% as protein. The main source of energy came from a nonprotein liquid formula (product 80056, Protein-Free Powder; Mead Johnson, Evansville, IN). The nitrogen component was provided as crystalline L-amino acids with an amino acid profile reflecting that of egg protein. The only amino acids that diverged from this profile were phenylalanine, lysine, tyrosine, and alanine. The phenylalanine intake was fixed at 9.0 mg•kg-1•d-1. The phenylalanine intake was chosen to represent the estimated mean adult requirement based on direct amino acid oxidation methods (1). The intake of the indicator amino acid for the study, lysine, was fixed at 45 mg•kg-1•d-1, the estimated safe intake for men (14, 15). Subjects received each of 7 tyrosine intakes (3.0, 4.5, 6.0, 7.5, 9.0, 10.5, and 12.0 mg•kg-1•d-1) in random order. Alanine intake was adjusted to maintain a constant nitrogen intake.

Tracer protocol
The isotopically labeled compounds used in the study were NaH13CO3 (99% 13C; Isotec Inc, Miamisburg, OH) and L-[1-13C] lysine (99% 13C; Isotec Inc). Quality-control tests were performed by the manufacturer of the isotopes. Chemical purity and the specified isotopic enrichment and position were confirmed by nuclear magnetic resonance, whereas the isomeric purity was determined with gas chromatography–mass spectrometry (GC-MS). Solutions of each tracer were prepared in deionized water and stored at -20°C until used. Before being dispensed, isotope solutions were sterilized by passage through a 0.22-µm filter (Millipore Corporation, Bedford, MA).

The oral tracer-infusion protocol began at 1000 on the study day after the subjects underwent adaptation to enteral intake for 4 h, which ensured sufficient time for 13CO2 background equilibration in expired carbon dioxide (16). A bolus dose of 0.172 mg NaH13CO3/kg and 2.4 mg L-[1-13C]lysine/kg was given to prime the bicarbonate and lysine pools, respectively. In addition to the priming dose, the subjects were given 1.2 mg L-[1-13C]lysine/kg hourly throughout the remaining 6 h of the study. Isotopes were given with the hourly meals.

Sample collection
Three baseline blood and expired breath 13CO2 samples were collected 10, 20, and 30 min before the isotope protocol began. Blood and breath samples were collected at isotopic steady state (plateau) every 30 min during the period 210–330 min after the isotope protocol began. Blood specimens were sampled from a 21-gauge needle inserted into a superficial dorsal vein on the hand. The blood in the hand region was arterialized by placing the subject's hand in a warming device (17) maintained at 60°C for 15 min before sample collection. Blood specimens (2 mL) were drawn into heparin-containing syringes (Aspirator; Marquest Medical Products, Inc, Englewood, CO) and immediately placed on ice until centrifuged. Plasma was separated from the sample by centrifugation at 1500 x g for 20 min at 4°C and then was transferred into microcentrifuge tubes and stored at -20°C until analyzed for L-[1-13C]lysine enrichment and phenylalanine and tyrosine concentrations.

The production rate of expired carbon dioxide (CO2) was measured during the baseline period of each study day with an indirect calorimeter (2900 Computerized Energy Measurement System; Sensormedics, Yorba Linda, CA). Carbon dioxide was collected by bubbling a sample (500 mL/min) of the expired carbon dioxide collected from a ventilated mask through a modified reflux container containing 10 mL NaOH for 7 min (18). The sample was subsequently transferred into collection tubes (Vacutainer 6441, 100 x 16 mm; Becton Dickinson Inc, Mississauga, Canada) for storage at -20°C until analyzed for 13C enrichment.

Analytic procedures and calculations
The enrichment of plasma amino acids was analyzed by the method of Patterson et al (19) by using gas chromatography– mass spectrometry. Briefly, plasma samples (200 µL) were deproteinized with an equal volume of 20% (wt:vol) trichloroacetic acid followed by centrifugation at 9000 x g for 5 min at 23°C in microcentrifuge tubes. The supernate was transferred from the tubes to columns containing a cationic ion exchange resin (1.5 mL) (Dowex 50W-X8, 100–200 mesh, H+ form; Bio-Rad Laboratories, Hercules, CA) for amino acid separation. The effluent solution was freeze-dried (Freezone 12 L; Labconco Corp, Kansas City, MO) before derivatization to its N,O-heptafluorobutyryl n-propyl esters.

The first step of the derivatization process involved esterification of the amino acids by adding 500 µL acetylpropanol prepared fresh each day by reacting acetyl chloride with propanol over ice at a ratio of 1:5. Samples were vortex mixed, heated at 110°C for 1 h, and dried under a steady stream of nitrogen gas at <40°C. After being dried, 50 µL of the derivative heptafluorobutyric anhydride was added to the samples, vortex mixed, and heated at 60°C for 20 min. Samples were then dried, topped with nitrogen gas, and stored at -20°C until analyzed. When ready for analysis, samples were reconstituted in 100 µL hexane.

Amino acid separation was performed on a gas chromatograph (GC model 5890 Series 2; Hewlett Packard, Mississauga, Canada) attached to a quadrupole mass spectrometer (Trio-2; Vacuum Generator Micromass, Cheshire, United Kingdom). Derivatized amino acids were splitlessly introduced into the instrument by automatic injector (model 7673 injector; Hewlett Packard). Separation was performed on a 30 m x 0.32 mm (inner diameter) x 1.0 µm (film thickness) fused silica capillary column (model HP-5; Hewlett-Packard) with helium serving as a carrier gas.

The GC column was coupled directly to the ion source set at a temperature of 160°C and operated under conditions of negative chemical ionization. Ammonia was used as reactant gas. Selected ion chromatograms were obtained by monitoring the mass-to-charge ratio of 360 and 361 for the M and M+1 species of lysine, respectively. Areas under the peaks were integrated by using a Digital DECp 450D2LP computer (Digital Instruments, Santa Barbara, CA) with Lab-Base software (Biotech, Cheshire, United Kingdom). Concentrations of phenylalanine and tyrosine were determined by GCMS by using the internal standard technique described by Wolfe (20).

Expired 13CO2 enrichment was measured by isotope ratio mass spectrometry as described previously (18). CO2, collected from a ventilated-hood system was measured indirectly by using a carbon dioxide analyzer (1400 series; Servomex; Westech Industrial Ltd, Mississauga, Canada) and mass flow meter (5860 series, Brooks; Trillium Measurement and Control, Stouffville, Canada). 13CO2 enrichment was measured with a dual-inlet magnetic sector isotope ratio mass spectrometer (model 602D; Vacuum Generator Micromass, Cheshire, United Kingdom). Trapped carbon dioxide in the form of Na2CO3 was released by reacting a 0.5-mL sample with an equal volume of 85% phosphoric acid within an evacuated Rittenburg tube. The carbon dioxide gas was isolated from the aqueous phase by immersing the tube in a bath of methanol and dry ice to freeze the liquid, without restricting movement of the gas. Enrichment measures were expressed as atoms percent excess (APE) 13CO2 over a reference standard of compressed carbon dioxide gas. Regular repeat analysis of a standard from the National Institute of Standards and Technology (NBS no. 20, PDB limestone; Gaithersburg, MD) gave a CV of 0.2%.

Model of amino acid metabolism and calculations
Whole-body lysine flux was calculated from the dilution of isotope in the body amino acid pool at isotopic steady state (21):


where Qlys is the rate of lysine flux, i is the isotope infusion rate (µmol•kg-1•h-1), Ei is the enrichment of the infused isotope (APE) and Ep is the enrichment of the amino acid in the plasma at isotopic steady state (plateau, in units of APE).

The rate of lysine oxidation was calculated as described by Matthews et al (21):


where Olys represents lysine oxidation and 13CO2 represents the rate of 13CO2 released by lysine tracer oxidation (µmol•kg-1•h-1) calculated with the following equation:


where CO2 is in cm3/min, ECO2 is 13CO2 enrichment in expired breath at isotopic steady state (APE), the constants 44.6 µmol/cm3 and 60 min/h convert CO2 to µmol/h, the factor of 100 changes APE to a fraction, W is the weight (kg) of the subject, and 13CO2 retained by the body as bicarbonate is corrected by using a retention factor (RF).

Statistical analyses
The study followed a completely randomized design with tyrosine intake as the independent variable. A three-way analysis of variance was carried out to determine the effect of individual, order of study, and tyrosine intake on 13CO2, oxidation, and lysine flux. Regression models (linear, quadratic, and linear regression crossover) (22) were fitted to the data to determine the relation that best described the response of the dependent variables 13CO2 and lysine oxidation to increasing tyrosine intakes. The regression analyses were performed by the method of least squares by using the regression procedure of SAS (23). The best model was determined on the basis of factors relating to model fit and variation. Plasma amino acid concentrations were analyzed by two-way analysis of variance with tyrosine intake and subject included in the model as main effects. When warranted, post hoc analysis was performed with Duncan's new multiple-range test. All statistical analyses and data modeling were performed by using SAS (23).


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
There were significant differences in plasma tyrosine concentrations after 8 h of feeding, which were highest at tyrosine intakes >6 mg•kg-1•d-1, except for the highest tyrosine intake (12 mg•kg-1•d-1), at which plasma tyrosine concentrations were not significantly different from those at an intake of 6 mg•kg-1•d-1 (Figure 1Go). Although there were significant differences in the phenylalanine concentration after 8 h of feeding at different tyrosine intakes, there was no trend (Figure 2Go).



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  		FIGURE 1. . Mean (±SEM) plasma tyrosine concentrations in healthy men after 8 h of consuming the study diet. Bars with different superscript letters are significantly different, P < 0.05.

 


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  		FIGURE 2. . Mean (±SEM) plasma phenylalanine concentrations in healthy men after 8 h of consuming the study diet. Bars with different superscript letters are significantly different, P < 0.05.

 
Lysine flux estimates are shown in Table 2Go. Tyrosine intake and order of study day did not affect lysine flux significantly within individuals. There was, however, a subject effect on lysine flux. There was a main effect of tyrosine intake (P < 0.003) on the estimate of 13CO2, but not of individual or order. Data for the tyrosine intake of 3 mg•kg-1•d-1 is missing for one subject because of a technical difficulty with the sample collection. The mean (±SEM) 13CO2 values at each tyrosine intake are shown in Figure 3Go. In general, 13CO2 decreased from tyrosine intakes of 3.0 to 6.0 mg•kg-1•d-1, after which point there was no change (slope not significantly differently different from zero) with further increases in tyrosine intake. Regression analysis showed that the two-phase linear regression crossover model was the best fit to the data. The breakpoint estimate, representative of the mean requirement, was estimated to be 6.0 mg•kg-1•d-1. The upper 95% CI, which was calculated from variation about the estimate and represented the safe population requirement, was estimated to be 7.0 mg•kg-1•d-1.


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  		TABLE 2. Effect of tyrosine intake and subject on lysine flux1
 


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  		FIGURE 3. . Mean (±SEM) production of 13CO2 (13CO2) from the oxidation of L-[1-13C]lysine at graded tyrosine intakes. Dotted vertical lines represent the 95% confidence limits of the breakpoint (6.0 mg•kg-1•d-1) estimate (r2 = 0.4, P < 0.001).

 
The oxidation rates of individual subjects are shown in Table 3Go. In general, the oxidation estimate, calculated from plasma lysine enrichment, was more variable than were the 13CO2 values that were measured directly. Nevertheless, analysis of variance showed a significant effect of tyrosine intake and subject on lysine oxidation. However, the two-phase linear regression crossover analysis did not result in a significant model; therefore, estimates of requirements were not made with use of the oxidation estimate.


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  		TABLE 3. Effect of tyrosine intake and subject on lysine oxidation1
 

   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
The present study estimated the mean tyrosine requirement of healthy men receiving an average intake of dietary phenylalanine to be 6 mg•kg-1•d-1. The safe population estimate of tyrosine intake calculated from the upper 95% confidence limit of the breakpoint analysis was 7 mg•kg-1•d-1. These data are important because they represent the first estimate of requirement of a dispensable amino acid in adult humans. The provision of excess tyrosine was shown to cause excess phenylalanine to be directly oxidized as opposed to equilibrating with the whole-body tyrosine pool (10, 11) and hence was available to meet tyrosine needs. This characteristic of phenylalanine metabolism within the hepatocyte enabled the need for phenylalanine to be distinguished from that for total aromatic amino acids. Fixing the phenylalanine intake at the average requirement provided an adequate phenylalanine intake without an excess that could potentially be used as a source of tyrosine. This phenylalanine intake results in an inadequate total aromatic amino acid intake until an adequate intake of tyrosine is provided. This design, in turn, allowed for the isolation of tyrosine requirements from that for phenylalanine.

A breakpoint was identified when the data points of 13CO2 from the oxidation of L-[1-13C]lysine were partitioned between 2 linear regression equations. 13CO2 is the primary outcome measure used for determining amino acid requirements (24) because it was shown consistently to be less variable and more sensitive than the respective amino acid oxidation estimate based on plasma enrichment of the test amino acid (25, 26). The greater variation of the oxidation estimate is believed to be due to the observation that plasma amino acid enrichment is an inaccurate estimate of the intracellular pool for oxidation (27). Because 13CO2 can only arise from the enriched amino acid at the site of oxidation, it is considered to be a more sensitive and more specific responder to changes in the test amino acid intake (26, 28–30).

This is the first time that lysine has been used as an indicator amino acid in adult humans. To serve as an indicator, the amino acid must be indispensable and the labeled carboxyl carbon must be irreversibly oxidized to carbon dioxide. Furthermore, the pool and flux of the indicator should not be altered by changing the intake of the test amino acid (25, 31). Because the flux of the indicator is partitioned between oxidation and incorporation into protein, the total flux remains the same (31). Although phenylalanine has proven to be an effective indicator for amino acid requirement studies in animals (28–30) and humans (24–26), the present study provides evidence that lysine is also an effective indicator amino acid.

At a fixed phenylalanine intake of 9.0 mg•kg-1•d-1, the mean and safe tyrosine requirements in men were found to be 6.0 and 7.0 mg•kg-1•d-1, respectively. The resultant average requirement and safe total aromatic amino acid intake were 15 and 21 mg•kg-1•d-1, respectively. The balance of aromatic amino acids determined from the mean estimates of phenylalanine and tyrosine requirements was 60:40 (phenylalanine:tyrosine). This balance of aromatic amino acids was similar to that determined in neonatal pigs (54:46) (5, 6), piglet tissue (57:43) (32), and human fetal tissue (59:41) (33). These data suggest that the ideal balance of aromatic amino acids, which supports the maximum efficiency of amino acid utilization, is within a narrow range of phenylalanine and tyrosine intakes. These findings could benefit individuals with conditions associated with altered aromatic metabolism such as hepatic (34, 35) or renal (36, 37) disease.

Sanchez et al (2, 3) and Basile-Filho et al (4, 8) carried out extensive 24-h amino acid balance studies using stable isotope tracers of phenylalanine and tyrosine to examine aromatic amino acid metabolism and the adequacy of phenylalanine intake. This approach defines the requirement as the minimum intake needed to equal obligatory amino acid catabolism. These authors used 2 catabolic indexes, phenylalanine hydroxylation and oxidation, and studied subjects receiving 1 of 3 phenylalanine intakes (21.9, 39, and 100 mg•kg-1•d-1) in a diet that contained little tyrosine. The collective evidence from these studies suggests that an intake of 21.9 mg•kg-1•d-1 was inadequate as indicated by the negative phenylalanine balance estimated from the difference between phenylalanine input and oxidation or hydroxylation. Individuals who received phenylalanine intakes of 100 and 39 mg•kg-1•d-1, in contrast, were generally in positive phenylalanine balance. Therefore, the data from those studies suggest that the total aromatic amino acid requirement is between 21.9 and 39 mg•kg-1•d-1, which is higher than the requirement estimated in the present study. The mean total aromatic amino acid requirement for men estimated previously by Rose et al (38) was 13.3 mg•kg-1•d-1; the safe intake (+2 SD) was estimated to be 17.1 mg•kg-1•d-1. Comparable estimates in women ranged from 14 to 18 mg•kg-1•d-1 (39). These estimated requirements are lower than our estimated safe intake of 21.0 mg•kg-1•d-1. It is important to note that neither of the 2 previous nitrogen balance studies included miscellaneous nitrogen losses. A recent reanalysis of lysine requirements determined on the basis of nitrogen balance showed that when miscellaneous nitrogen losses are accounted for, the estimated lysine requirement increases significantly (40).

There are several possible reasons that our results differ from those of Sanchez et al (2, 3) and of Basile-Filho et al (4, 8). First, provision of aromatic amino acids in an ideal balance, such as in the present experiment, likely maximized the utilization efficiency of the aromatic amino acids such that the estimated total aromatic amino acid requirement was lower than what would have been estimated if all aromatic amino acids were given as phenylalanine. Sanchez et al (3) discussed the likelihood that intake of a preformed source of tyrosine may improve aromatic amino acid homeostasis. Second, their estimates of phenylalanine catabolism were based on either phenylalanine oxidation or hydroxylation. Both estimates are dependent on precursor pool enrichment estimates, which, as discussed above, contribute considerable variation to the estimates and can result in incorrect results for phenylalanine hydroxylation (7). Third, the 24-h aromatic amino acid balance studies included a several-day adaptation period to the test amino acid, whereas, apart from a 2-d adaptation to a protein intake of 1 g•kg-1•d-1, our subjects were adapted only for a matter of 6–8 h on the study day to the test amino acid. During the 2-d adaptation to protein intake, we calculated that subjects were also receiving {approx}43 mg phenylalanine•kg-1•d-1 and 39 mg tyrosine•kg-1•d-1. On the day of each indicator oxidation study, the subjects consumed the test intake of tyrosine and the fixed phenylalanine intake of 9 mg•kg-1•d-1. It was assumed that this lack of prior adaptation would result in a higher estimated requirement (41–43); however, the total aromatic amino acid requirement determined in the present study was actually slightly lower than that derived from the 24-h balance studies. The requirement, however, was higher than the earlier nitrogen balance–based estimates, which included adaptation periods of >=5–7 d. Finally, the tyrosine requirement was estimated by partitioning the oxidation of the indicator amino acid, lysine, to a 2-phase linear regression crossover analysis. This model involves the study of 6–7 test amino acid intakes carried out in the same subject, which allows for a precise mathematic estimate of requirement. The 24-h balance studies, because of their cost, difficulty, and complexity, have only studied 3 aromatic amino acid intakes, making an exact estimate of requirement difficult. Nonetheless, future work is needed to determine whether prior adaptation to tyrosine would have altered the estimates obtained in this experiment.


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Zello GA, Pencharz PB, Ball RO. Phenylalanine flux, oxidation, and conversion to tyrosine in humans studied with L-[1-13C]phenylalanine. Am J Physiol 1990;259:E835–43.[Abstract/Free Full Text]
  2. Sanchez M, El-Khoury AE, Castillo L, Chapman TE, Young VR. Phenylalanine and tyrosine kinetics in young men throughout a continuous 24-h period, at a low phenylalanine intake. Am J Clin Nutr 1995;61:555–70.[Abstract/Free Full Text]
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  4. Basile-Filho A, El-Khoury AE, Beaumier L, Wang SY, Young VR. Continuous 24-h L-[1-13C]phenylalanine and L-[3,3-2H2]tyrosine oral-tracer studies at an intermediate phenylalanine intake to estimate requirements in adults. Am J Clin Nutr 1997;65:473–88.[Abstract/Free Full Text]
  5. House JD, Pencharz PB, Ball RO. Tyrosine kinetics and requirement during total parenteral nutrition in the neonatal piglet: the effect of glycyl-L-tyrosine supplementation. Pediatr Res 1997;41:575–83.[Medline]
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  7. House JD, Thorpe JD, Wykes LJ, Pencharz PB, Ball RO. Evidence that phenylalanine hydroxylation rates are over-estimated in neonatal subjects receiving total parenteral nutrition with high phenylalanine content. Pediatr Res 1998;43:461–6.[Medline]
  8. Basile-Filho A, Beaumier L, El-Khoury AE, et al. Twenty-four–hour L-[1-13C]tyrosine and L-[3,3-2H2]phenylalanine oral tracer studies at generous, intermediate, and low phenylalanine intakes to estimate aromatic amino acid requirements in adults. Am J Clin Nutr 1998;67:640–59.[Abstract]
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  13. Moss AR, Schoenheimer R. The conversion of phenylalanine to tyrosine in normal rats. J Biol Chem 1940;135:415–29.[Free Full Text]
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  16. Bross R, Ball RO, Pencharz PB. Development of a minimally invasive protocol for determination of phenylalanine and lysine kinetics, in humans, during the fed state. J Nutr 1998;128:1913–9.[Abstract/Free Full Text]
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Received for publication September 3, 1999. Accepted for publication June 5, 2000.




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