Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-23T18:48:52.939Z Has data issue: false hasContentIssue false

Conversion of [15N]ammonia into urea and amino acids in humans and the effect of nutritional status

Published online by Cambridge University Press:  09 March 2007

P. J. M. Weijs
Affiliation:
Rowett Research Institute, Greenburn Road, Bucksburn, AberdeenAB2 9SB
A. G. Calder
Affiliation:
Rowett Research Institute, Greenburn Road, Bucksburn, AberdeenAB2 9SB
E. Milne
Affiliation:
Rowett Research Institute, Greenburn Road, Bucksburn, AberdeenAB2 9SB
G. E. Lobley
Affiliation:
Rowett Research Institute, Greenburn Road, Bucksburn, AberdeenAB2 9SB
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Hepatic NH3 detoxification by ureagenesis requires an input of aspartate-N, originating either from amino acid-N or NH3-N. The relative importance of these two routes may depend on the nutritional state. To test this, four volunteers were given a liquid diet for 2 d and then on day 3 were either fed every 20 min or fasted. Doses of 15NH4Cl were taken orally every 20 min for 6 h (total 1.5 g) and blood was sampled hourly. Urea-N elimination under fasted conditions was only 0.75 of that for the fed state. Considering the increase in body urea pool during feeding, ureagenesis during fasting was probably closer to 0.6 of that during feeding. Since the [14N15N] urea enrichment was not different between the fed and fasted states, the proportion of the 15NH3 dose converted to urea during fasting was also 0.6 of that during the fed condition. No change in [14N15N] urea and [amide-15N] glutamine enrichment suggested that NH3 enrichment was also not affected by nutritional state. Enrichment of [14N15N] urea was approximately 0.05 that of [14N15N] urea which indicates that 15NH3 can also enter the aspartate route, the importance of which is yet unknown. Both [15N15] urea and [amino-15N]glutamine enrichment in the fasted state were approximately 1.7 times that in the fed state, indicating increased labelling of precursors and/or increased NH3 flux through the aspartate route. Glutamate, valine, leucine and isoleucine showed comparable increases in enrichment during fasting. Arginine enrichment was unaltered by nutritional state, but was lower than [14N15N] urea, indicating incomplete equilibration with the arginine pool in periportal hepatocytes. The present study indicates that hepatic NH3 detoxification may use the aspartate route, gaining importance in the fasted state. The majority of urea was supplied with only one N atom from NH3, thus provision of the other may have consequences for alternative substrates, in particular amino acids.

Type
Human and Clinical Nutrition
Copyright
Copyright © The Nutrition Society 1996

References

REFERENCES

Barbul, A. (1985). Arginine: biochemistry, physiology, and therapeutic implications. Journal of Parenteral and Enteral Nutrition 10, 227238.CrossRefGoogle Scholar
Bässler, K. H. (1993). Metabolic and nutritional aspects of glutamate. In Glutamate - Transmitter and Toxi. Klinische Ernährungn 36, pp. 129135 [Kempski, O., editor]. München: Zuskschwerdt Verlag.Google Scholar
Calder, A.G. & Smith, A. (1988). Stable isotope ratio analysis of leucine and ketoisocaproic acid in blood plasma by gas chromatography/mass spectrometry. Use of the tertiary butyldimethylsilyl derivatives. Rapid Communications in Mass Spectrometry 2, 1416.CrossRefGoogle ScholarPubMed
Campbell, I. M. (1974). Incorporation and dilution values - their calculation in mass spectrally assayed stable isotope labelling experiments. Bioorganic Chemistry 3, 386397.CrossRefGoogle Scholar
Castillo, L., Chapman, T. E., Sanchez, M., Yu, Y.-M., Burke, J. F., Ajami, A. M., Vogt, J. & Young, V. R. (1993). Plasma arginine and citrulline kinetics in adults given adequate and arginine-free diets. Proceedings of the National Academy of Sciences, USA 90, 77497753.CrossRefGoogle ScholarPubMed
Cooper, A. J. L., Nieves, E., Coleman, A. E., Filc-DeRicco, S. & Gelbard, A. S. (1987). Short-term metabolic fate of [13N]ammonia in rat liver in vivo. Journal of Biological Chemistry 262, 10731080.CrossRefGoogle ScholarPubMed
Darmaun, D., Matthews, D. E. & Bier, D. M. (1986). Glutamine and glutamate kinetics in humans. American Journal of Physiology 251, E117E126.Google ScholarPubMed
Häussinger, D. (1990). Nitrogen metabolism in liver: structural and functional organization and physiological relevance. Biochemical Journal 267, 281290.CrossRefGoogle ScholarPubMed
Lobley, G. E., Connell, A., Lomax, M. A., Brown, D. S., Milne, E., Calder, A. G. & Farningham, D. A. H. (1995). Hepatic detoxification of ammonia in the ovine liver: possible consequences for amino acid catabolism. British Journal of Nutrition 73, 667685.CrossRefGoogle ScholarPubMed
Long, C. L., Jeevanandam, M. & Kinney, J. M. (1978). Metabolism and recycling of urea in man. American Journal of Clinical Nutrition 31, 13671382.CrossRefGoogle ScholarPubMed
Luo, Q. J., Maltby, S. A., Lobley, G. E., Lomax, M. A. & Calder, A.G. (1994). The effect of amino acids upon the pathways of 15NH4Cl conversion to urea in isolated sheep hepatocytes. Proceedings of the Nutrition Society 53, 197A.Google Scholar
Meijer, A. J., Lamers, W. H. & Chamuleau, A. F. M. (1990). Nitrogen metabolism and ornithine cycle function. Physiological Reviews 70, 701748.CrossRefGoogle ScholarPubMed
Milano, G. D., Lomax, M. A. & Lobley, G. E. (1996). Estimation of the enrichment of urea N precursors. Proceedings of the Nutrition Society 55, 42A.Google Scholar
Nieto, R., Calder, A. G., Anderson, S. E. & Lobley, G. E. (1996). Method for the determination of 15NH3 enrichment in biological samples by gas chromatography/electron impact ionisation mass spectrometry. Journal of Mass Spectrometry 31, 209294.3.0.CO;2-Z>CrossRefGoogle Scholar
Nissim, I., Yudkoff, M. & Lapidot, A. (1984). Simultaneous determination of [2-15N]- and [5-15N]glutamine with gas chromatography-mass spectrometry: applications to nitrogen metabolic studies. Analytical Biochemistry 143, 1420.CrossRefGoogle ScholarPubMed
Patterson, B. W., Carraro, F. & Wolfe, R. R. (1993). Measurement of 15N enrichment in multiple amino acids and urea in a single analysis by gas chromatography/mass spectrometry. Biological Mass Spectrometry 22, 518523.CrossRefGoogle Scholar
Reynolds, C. K. (1992). Metabolism of nitrogenous compounds by ruminant liver. Journal of Nutrition 122, 850854.CrossRefGoogle ScholarPubMed
Seal, C. J. & Reynolds, C. K. (1993). Nutritional implications of gastrointestinal and liver metabolism in ruminants. Nutrition Research Reviews 6, 185208.CrossRefGoogle ScholarPubMed
Stein, T. P., Leskiw, M. J. & Wallace, H. W. (1976). Metabolism of parenterally administered ammonia. Journal of Surgical Research 21, 1720.CrossRefGoogle ScholarPubMed
Summerskill, W. H. J. & Wolpert, E. (1970). Ammonia metabolism in the gut. American Journal of Clinical Nutrition 23, 633639.CrossRefGoogle ScholarPubMed
Weijs, P. J. M., Calder, A. G. & Lobley, G. E. (1994 a). Conversion of 15N-ammonia into urea and glutamine in humans and the effect of nutritional status. Proceedings of the 2nd World Conjerence on Stable Isotopes in Nutritional and Metabolic Research,Rotterdam, The Netherlands, A18.Google Scholar
Weijs, P. J. M., Calder, A.G. & Lobley, G. E. (1994 b). Incorporation of 15N-ammonia into urea and amino acids as influenced by fasting and feeding in man. Proceedings of the Nutrition Society 53, 200A.Google Scholar