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The fate of absorbed and exogenous ammonia as influenced by forage or forage–concentrate diets in growing sheep

Published online by Cambridge University Press:  09 March 2007

G. E. Lobley
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB2 9SB
P. J. M. Weijs
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB2 9SB
A. Connell
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB2 9SB
A. G. Calder
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB2 9SB
D. S. Brown
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB2 9SB
E. Milne
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB2 9SB
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Abstract

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Changes in splanchnic energy and N metabolism were studied in sheep, prepared with vascular catheters across the portal-drained viscera (PDV) and the Liver, and maintained on supramaintenance intakes of either grass or grass + barley pellets. The animals were challenged, on both diets, with 4 d intra- mesenteric vein infusions of NH4CI (25 µmol/min) plus NH4HCO3 (at either 0 or 125 µmol/min). On the final day of each treatment the natural abundance NH4Cl was replaced with 15NH4Cl over a 10 h infusion while over the same period [l-13C]leucine was infused via a jugular vein. Measurements were made of blood flow plus mass transfers of NH3, urea, free amino acids and O2, across the PDV and liver. Enrichments of [14N15N]urea and [15N15N]urea plus [15N]glutamine, aspartate and glutamate were also monitored. Whole-body urea flux was determined by infusion of [14C]urea. At the end of the study the animals were infused for 3 h with 15NH4CI, killed and liver samples assayed for intracellular free amino acid enrichments and concentrations. Blood flows across the splanchnic region were unaffected by either diet or level of ammonium salt infusion. At the lower ammonium salt infusion there was a trend for greater absorption of NH3 across the PDV (P<0·10) with grass + barley than with the grass diet, while removal of urea was unaltered. At the higher ammonium salt infusions there was a significantly greater appearance of NH, across the PDV and this exceeded the extra infused. Urea-N removal, however, was also elevated and by more than that required to account for the additional NH3. The PDV contributed 19–28% to whole-body O2 consumption and the liver 23–32%. Hepatic extraction of absorbed NH3 was complete on all treatments and systemic pH remained constant. The fractions of urea-N apparently derived from NH3, were similar on the grass (0·59–0·64) and grass + barley (0·64–0·67) diets. Hepatic production of urea agreed well with urea flux measurements. Between the two levels of ammonium salt infusion and within diets the additional NH3 removed across the PDV was accounted for by the increased urea-N production. The [14N15N]: [15N15N] ratio of the urea produced was 97:3, while the enrichment of hepatic intracellular free aspartate was lower than that of [14N15N]urea. Glutamine enrichments were 0·23–0·37 those of [14N15N]urea, indicating a minor role for those hepatocytes (probably perivenous) which contain glutamine synthetase (EC 6.3.1.2). Leucine kinetics, either for the whole body or splanchnic tissues, were not different between diets or level of ammonium salt infusion, except for oxidation which was less on the grassfbarley ration. Amino acid concentrations were lower on the grass + barley diet but net PDV absorptions were similar. The pattern of essential amino acids absorbed into the PDV showed good agreement with the published composition of mixed rumen microbial protein. Fractional disappearances of absorbed free essential amino acids across the liver varied from 0·4 (branched chains) to near unity (histidine, phenylalanine)

Type
Animal Nutrition
Copyright
Copyright © The Nutrition Society 1996

References

REFERENCES

Bean, E. S. & Atkinson, D. E. (1984). Regulation of the rate of urea synthesis in liver by extracellular pH. A major factor in pH homeostasis in mammals. Journal of Biological Chemistry 259, 15521559.CrossRefGoogle Scholar
Blaxter, K. L., Brockway, J. M. & Boyne, A. W. (1972). A new method for estimating the heat production of animals. Quarterly Journal of Experimental Physiology 57, 672.Google ScholarPubMed
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
Cheung, C. -W., Cohen, N. S. & Raijman, L. (1989). Channelling of urea cycle intermediates in situ in permeabilized hepatocytes. Journal of Biological Chemistry 264, 40384044.CrossRefGoogle ScholarPubMed
Cohen, N. S., Cheung, C. -W. & Raijman, L. (1987). Channelling of extramitochondrial ornithine to matrix ornithine transcarbamoylase. Journal of Biological Chemistry 262, 203208.CrossRefGoogle Scholar
Cooper, A. J. L., Nieves, E., Coleman, A. E., Filc-De Ricco, 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
Covolo, G. C. & West, R. (1947). The activity of arginase in red blood cells. Journal of Clinical Endocrinology 7, 325330.CrossRefGoogle ScholarPubMed
Demigné, C., Yacoub, C., Morand, C. & Rémésy, C. (1991). Interactions between propionate and amino acid metabolism in isolated sheep hepatocytes. British Journal of Nutrition 65, 301317.CrossRefGoogle ScholarPubMed
Derr, R. F. & Zieve, L. (1982). Methanethiol and fatty acids depress urea synthesis by the isolated perfused rat liver. Journal of Laboratory and Clinical Medicine 100, 585592.Google ScholarPubMed
Fitch, N. A., Gill, M., Lomax, M. A. & Beever, D. E. (1989). Nitrogen and glucose metabolism by the liver of forage- and forage-concentrate-fed cattle. Proceedings of the Nutrition Society 48, 76A.Google Scholar
Ganvacki, S., Wiechetek, M., Karlik, W., Souffrant, W.-B. & Krawielitzki, K. (1990). Effect of propionate on the utilisation of nitrogen from 15NH4Cl for urea synthesis in hepatocytes isolated from sheep liver. International Journal of Biochemistry 22, 11811188.Google Scholar
Harris, P. M., Lobley, G. E., Skene, P. A., Buchan, V., Calder, A. G., Anderson, S. E. & Connell, A. (1992). Effect of food intake on hind-limb and whole-body protein metabolism in young growing sheep: chronic studies based on arterio-venous techniques. British Journal of Nutrition 68, 388407.CrossRefGoogle ScholarPubMed
Häussinger, D., Lamers, W. H. & Moorman, A. F. M. (1992). Hepatocyte heterogeneity in the metabolism of amino acids and ammonia. Enzyme 46, 7293.CrossRefGoogle Scholar
Heitmann, R. N. & Bergman, E. N. (1978). Glutamine metabolism, interorgan transport and glucogenicity in the sheep. American Journal of Physiology 234, E197–E203.Google ScholarPubMed
Heitmann, R. N. & Bergman, E. N. (1980). Transport of amino acids in whole blood and plasma of sheep. American Journal of Physiology 239, E242–E247.Google ScholarPubMed
Huntington, G. B. (1989). Hepatic urea synthesis and site and rate of removal from blood of beef steers fed alfalfa or a high concentrate diet. Canadian Journal of Animal Science 69, 215223.CrossRefGoogle Scholar
Jackson, A. A., GoldenM. H, N. M. H, N., Jahoor, P. F. & Landman, J. P. (1980). The isolation of urea nitrogen and ammonia nitrogen from biological samples for mass spectrometry. Analytical Biochemistry 105, 1417.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
Lobley, G. E., Connell, A., Revell, D. K., Bequetle, B. J., Brown, D. S. & Calder, A. G. (1996). Splanchnic-bed transfers of amino acids in sheep blood and plasma, as monitored through use of a multiple U-13C-labelled amino acid mixture. British Journal of Nutrition 75, 217235.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., Calder, G. & Lomax, M. A. (1995). The effect of amino acids on the metabolic fate of 15NH4CI in isolated sheep hepatocytes. European Journal of Biochemistry 228, 912917.CrossRefGoogle ScholarPubMed
Maltby, S. A., Lomax, M. A., Beever, D. E. & Pippard, C. J. (1991). The effect of increased ammonia and amino acid supply on post prandial portal-drained viscera and hepatic metabolism in growing steers fed maize silage. In Energy Metabolism of Farm Animals. EAAP Publication no. 58, pp. 2023 [Wenk, C. and Boessinger, M., editors]. Zurich: Schriftenreihe aus dem Institut für Nutztierwissenschaften Gruppe Ernährung.Google Scholar
Meijer, A. J., Lamers, W. H. & Chamuleau, R. 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). A new method for determination of 15NH3, enrichment in biological samples by gas chromatography/electron impact mass spectrometry. Journal of Mass Spectrometry 31, 289294.3.0.CO;2-Z>CrossRefGoogle Scholar
Patterson, B. W., Carraro, F. & Wolfe, R. R. (1993). Measurement of 15N enrichment of multiple amino acids and urea in a single analysis by gas chromatography/mass spectrometry. Biological Mass Spectrometry 22, 518523.CrossRefGoogle Scholar
Reaich, D., Channon, S. M., Scrimgeour, C. M. & Goodship, T. H. J. (1992). Ammonium chloride-induced acidosis increases protein breakdown and amino acid oxidation in humans. American Journal of Physiology 263, E735E739.Google ScholarPubMed
Reynolds, C. K. (1992). Metabolism of nitrogenous compounds by ruminant liver. Journal of Nutrition 122, 50854.CrossRefGoogle ScholarPubMed
Reynolds, C. K. & Tyrrell, H. F. (1991). Effects of mesenteric vein L-alanine infusion on liver metabolism in beef heifers fed on diets differing in forage:concentrate ratio, British Journal of Nutrition 66, 437450.CrossRefGoogle ScholarPubMed
Reynolds, C. K., Tyrrell, H. F. & Reynolds, P. J. (1991 a). Effects of diet forage-to-concentrate ratio and intake on energy metabolism in growing beef steers: whole body energy and nitrogen balance and visceral heat production. Journal of Nutrition 121, 9941003.CrossRefGoogle Scholar
Reynolds, C. K., Tyrrell, H. F. & Reynolds, P. J. (1991 b). Effects of diet forage-to-concentrate ratio and intake on energy metabolism in growing beef heifers: net nutrient metabolism by visceral tissues. Journal of Nutrition 121, 10041015.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
Stewart, P. M. & Walser, M. (1980). Failure of the normal ureagenic response to amino acids in the organhacid loaded rat: a proposed mechanism for the hyperammonemia of propionic and methymalonic acidemia. Journal of Clinical Investigation 66, 484492.CrossRefGoogle Scholar
Storm, E. & Ørskov, E. R. (1983). The nutritive value of rumen micro-organisms in ruminants. 1. Large scale isolation and chemical composition of rumen micro-organisms. British Journal of Nutrition 50, 463470.CrossRefGoogle ScholarPubMed
Walser, M., George, J. & Bodenlos, L. J. (1954). Altered proportions of isotopes of molecular nitrogen as evidence for a monomolecular reaction. Journal of Chemical Physics 22, 1146.CrossRefGoogle Scholar
Wilton, J. C., Gill, M. & Lomax, M. A. (1988). Uptake of ammonia across the liver of forage fed cattle. Proceedings of the Nutrition Society 47, 153A.Google Scholar