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Interactions among the branched-chain amino acids and their effects on methionine utilization in growing pigs: effects on nitrogen retention and amino acid utilization

Published online by Cambridge University Press:  09 March 2007

Stefan Langer
Affiliation:
Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB, UK
Malcolm F. Fuller*
Affiliation:
Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB, UK
*
*Corresponding author: Dr Malcolm Fuller, fax +44 (0)1224 716687, email [email protected]
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Abstract

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An experiment was conducted to investigate the effects of branched-chain amino acid (BCAA) interactions on their utilization by growing pigs and the effects of excessive amounts of BCAA (leucine, isoleucine, valine) on the utilization of methionine. A semipurified diet containing 100 g crude protein/kg with a balanced amino acid pattern was prepared using casein supplemented with free amino acids. Three further diets were made by reducing the concentration of methionine + cyst(e)ine, valine or isoleucine by 20 %. Each of these four diets was then supplemented with leucine (50 % excess) or a mixture of BCAA (50 % excess of each but excluding the limiting amino acid). All diets were isoenergetic and were made isonitrogenous by replacement of glutamic and aspartic acids. The twelve diets were given to twenty-four growing pigs (30–40 kg) in three periods according to a randomized block design. Each period lasted 8 d and N retention was measured during the last 5 d of each period. Reducing dietary methionine, valine or isoleucine reduced the utilization of N (N retained/N digested) by approximately 20 % (P < 0·05). Adding leucine to the isoleucine-limiting diet decreased the utilization of N by 9 % (P < 0·05). This was reversed by simultaneous addition of valine. Excess leucine in a valine-deficient diet did not significantly reduce N utilization. In methionine-limiting diets an excess of either leucine alone or of all three BCAA increased the utilization of N by 8 % (P < 0·05).

Type
Research Article
Copyright
Copyright © The Nutrition Society 2000

References

Aftring, RP, Block, KP & Buse, MG (1986) Leucine and isoleucine activate skeletal muscle branched-chain α-keto acid dehydrogenase in vivo. American Journal of Physiology 250, E599E604.Google ScholarPubMed
Bech-Andersen, S, Mason, VC & Dhanoa, MS (1990) Hydrolysate preparation for amino acid determinations in feed constituents. 9. Modifications to oxidation and hydrolysis conditions for streamlined procedures. Journal of Animal Physiology and Animal Nutrition 63, 188197.CrossRefGoogle Scholar
Benevenga, NJ (1984) Evidence for alternative pathways of methionine catabolism. In Advances in Nutritional Research, vol. 6, pp. 118 [Draper, HH, editor]. New York, NY: Plenum Press.Google Scholar
Benevenga, NJ & Haas, LG (1986) Isolation and identification of 3-methylthiopropionyl-CoA (MTP-CoA) and methanethiol from metabolism of α-keto-γ-methiolthiobutyrate (keto-met) and 3-methylthiopropionate (MTP) by pig liver mitochondria. Journal of Nutrition 116, XXIV, Abstr. 24.Google Scholar
Benton, DA, Harper, AE, Spivey, HE & Elvehjem, CA (1956) Leucine, isoleucine and valine relationships in the rat. Archives of Biochemistry and Biophysics 60, 147155.CrossRefGoogle ScholarPubMed
Block, KP (1989) Interactions among leucine, isoleucine, and valine with special to the branched-chain amino acid antagonism. In Absorption and Utilization of Amino Acids, vol. 1, pp. 229244 [Friedman, M, editor]. Boca Raton, FL: CRC Press.Google Scholar
Block, KP & Harper, AE (1984) Valine metabolism in vitro: effects of high dietary levels of leucine and isoleucine. Metabolism 33, 559566.CrossRefGoogle Scholar
Block, KP & Harper, AE (1991) High levels of dietary amino and branched-chain α-keto acids alter plasma and brain amino acid concentrations in rats. Journal of Nutrition 121, 663671.CrossRefGoogle ScholarPubMed
Block, KP, Soemitro, S, Heywood, BW & Harper, AE (1985) Activation of liver branched-chain α-keto acid dehydrogenase in rats by excesses of dietary amino acids. Journal of Nutrition 115, 15501561.CrossRefGoogle ScholarPubMed
Boyer, B & Odessey, R (1990) Quantitative control analysis of branched-chain 2-oxo acid dehydrogenase complex activity by feedback inhibition. Biochemical Journal 271, 523528.CrossRefGoogle ScholarPubMed
Calvert, CC, Klasing, KC & Austic, RE (1982) Involvement of food intake and amino acid catabolism in the branched-chain amino acids antagonism in chicks. Journal of Nutrition 112, 627635.CrossRefGoogle ScholarPubMed
Davidson, J, Mathieson, J & Boyne, AW (1970) The use of automation in determining nitrogen by the Kjeldahl method, with final calculation by computer. Analyst 95, 181193.CrossRefGoogle ScholarPubMed
D'Mello, JPF & Lewis, D (1970) Amino acid interactions in chick nutrition. 2. Interrelationships between leucine, isoleucine and valine. British Poultry Science 11, 313323.CrossRefGoogle ScholarPubMed
Frick, GP, Tai, L-R, Blinder, L & Goodman, HM (1981) L-Leucine activates branched chain α-keto acid dehydrogenase in rat adipose tissue. Journal of Biological Chemistry 256, 26182620.CrossRefGoogle ScholarPubMed
Fulks, RM, Li, JB & Goldberg, AL (1975) Effects of insulin, glucose, and amino acids on protein turnover in rat diaphragm. Journal of Biological Chemistry 250, 290298.CrossRefGoogle ScholarPubMed
Fuller, MF, Livingstone, RM, Baird, BA & Atkinson, T (1979) The optimal amino acid supplementation of barley for the growing pig. 1. Response of nitrogen metabolism to progressive supplementation. British Journal of Nutrition 41, 321331.CrossRefGoogle ScholarPubMed
Goldberg, AL & Tischler, ME (1981) Regulatory effects of leucine on carbohydrate and protein metabolism. In Metabolism and Clinical Implications of Branched Chain Amino and Ketoacids, pp. 205216 [Walser, M, and Williamson, JR, editors]. New York, NY: Elsevier, North-Holland.Google Scholar
Harper, AE, Benevenga, NJ & Wohlhueter, RM (1970) Effects of ingestion of disproportionate amounts of amino acids. Physiological Reviews 50, 428558.CrossRefGoogle ScholarPubMed
Harper, AE, Block, KP & Cree, TC (1983) Branched-chain amino acids: Nutritional and metabolic interrelationships. In Proceedings of the IVth Symposium on Protein Metabolism and Nutrition, Clermont-Ferrand (France), European Association of Animal Production Publication no. 31, vol. 1, pp. 159181 [Pion, R, Arnal, M and Bonin, D, editors]. Paris: INRA.Google Scholar
Henry, Y, Duée, PH & Rérat, A (1976) Isoleucine requirement of the growing pig and leucine–isoleucine interrelationship. Journal of Animal Science 42, 357364.CrossRefGoogle ScholarPubMed
Langer, S & Fuller, MF (1994) The effect of excessive amounts of branched-chain amino acids on amino acid utilization in growing pigs. Proceedings of the Nutrition Society 53, 108A.Google Scholar
Langer, S, Scislowski, PWD, Brown, DS, Dewey, P & Fuller, MF (2000) Interactions among the branched-chain amino acids and their effects on methionine utilization in growing pigs:. effects on plasma amino- and keto-acid concentrations and branched-chain keto-acid dehydrogenase activity British Journal of Nutrition 83, 4958.Google ScholarPubMed
Li, JB & Jefferson, LS (1978) Influence of amino acid availability on protein turnover in perfused skeletal muscle. Biochimica et Biophysica Acta 544, 351359.CrossRefGoogle ScholarPubMed
Livesey, G (1981) Metabolism of 'essential' 2-oxo acids by liver and a role for branched-chain oxo acid dehydrogenase in the catabolism of methionine. In Metabolism and Clinical Implications of Branched Chain Amino and Ketoacids, pp. 143148 [Walser, M, and Williamson, JR, editors]. New York, NY: Elsevier, North-Holland.Google Scholar
McNurlan, MA, Fern, EB & Garlick, PJ (1982) Failure of leucine to stimulate protein synthesis in vivo. Biochemical Journal 204, 831838.CrossRefGoogle ScholarPubMed
McNurlan, MA, Fern, EB & Garlick, PJ (1983) The effect of high doses of leucine on the protein synthesis in rat tissues. In Amino Acids. Metabolism and Medical Applications, pp. 188191 [Blackburn, GL, Grant, JP and Young, VR, editors]. Boston, MA: John Wright and Sons.Google Scholar
Meguid, MM, Schwarz, HP, Matthews, DE, Karl, IE, Young, VR & Bier, DM (1983) In vivo and in vitro branched-chain amino acid interactions. In Amino Acids. Metabolism and Medical Applications, pp. 147154 [Blackburn, GL, Grant, JP and Young, VR, editors]. Boston, MA: John Wright and Sons.Google Scholar
Naumann, C & Vassler, R (1993) Methodenbuch (Band III) Die chemische Untersuchung von Futtermitteln. Darmstadt: VDLUFA-Verlag.Google Scholar
Oestemer, GA, Hanson, LE & Meade, RJ (1973) Leucine–isoleucine interrelationship in the young pig. Journal of Animal Science 36, 674678.CrossRefGoogle ScholarPubMed
Parker, PJ & Randle, PJ (1978) Inactivation of rat heart branched-chain 2-oxo acid dehydrogenase complex by adenosine triphosphate. FEBS Letters 95, 153156.CrossRefGoogle Scholar
Tannous, RI, Rogers, QR & Harper, AE (1966) Effect of leucine–isoleucine antagonism on the amino acid pattern of plasma and tissues of the rat. Archives of Biochemistry and Biophysics 113, 356361.CrossRefGoogle ScholarPubMed
Taylor, AJ, Cole, DJA & Lewis, D (1984) Amino acid requirements of growing pigs. 5. The interactions between isoleucine and leucine. Animal Production 38, 257261.Google Scholar
Wang, TC & Fuller, MF (1989) The optimum dietary amino acid pattern for growing pigs. 1. Experiments by amino acid deletion. British Journal of Nutrition 62, 7789.CrossRefGoogle ScholarPubMed
Wang, TC & Fuller, MF (1990) The effect of the plane of nutrition on the optimum dietary amino acid pattern for growing pigs Animal Production 50, 155164.Google Scholar