Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-12-03T19:19:59.323Z Has data issue: false hasContentIssue false

Hepatic response to increased exogenous supply of plasma amino acids by infusion into the mesenteric vein of Holstein- Friesian cows in late gestation

Published online by Cambridge University Press:  09 March 2007

D. Wray-Cahen
Affiliation:
AFRC IGER, Hurley, Maidenhead SL6 5LR
J. A. Metcalf
Affiliation:
AFRC IGER, Hurley, Maidenhead SL6 5LR
F. R. C. Backwell
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB21 9SB
B. J. Bequette
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB21 9SB
D. S. Brown
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB21 9SB
J. D. Sutton
Affiliation:
AFRC IGER, Hurley, Maidenhead SL6 5LR
G. E. Lobley
Affiliation:
Rowett Research Institute, Bucksburn, Aberdeen AB21 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.

The hepatic responses of late gestation, dry dairy cows to acute (6 h) infusions of an amino acid (AA) mixture (Synthamin; 0.0, 1.1, 2.2, 4.4, 8.8 and 17.6 mmol/min) into the mesenteric vein were determined. Neither blood flow nor O2 consumption across the portal-drained viscera (PDV) and liver was significantly altered by infusion. Similarly, there were no effects on net absorption, or hepatic removal, of acetate, propionate, butyrate or NH3. Glucose PDV appearance was unchanged but hepatic glucose production increased (P = 0.032) by 0.2 mmol/min per mmol/min of AA infused. Additional extraction of alanine, glycine (both infused) and glutamine (not infused) by the liver was sufficient to account for most of the extra C required for glucose synthesis. The N that would be liberated from these glucogenic AA would also account for a large proportion of the increase in urea-N produced in response to the AA infusion. This supports the concept of a correlation between gluconeogenesis and ureagenesis. Furthermore, the amide-N liberated from the extracted glutamine would contribute up to 0.17 of hepatic NH3 flux and assist in balancing N inputs into the carbamoyl phosphate and arginosuccinate entry points of the ornithine cycle. Rates of fractional extraction of the various AA by the liver were best fitted by linear equations, indicating that even at the highest rates of administration (approximately twice maximal physiological absorption) the transport systems were not saturated. Hepatic fractional extractions of infused essential AA were highest for methionine (0.83) and phenylalanine (0.87) with the lowest proportion removed observed for valine (0.25), leucine (0.30), lysine (0.31) and isoleucine (0.49). For the non-essential AA, the highest apparent fractional extractions were for glycine (0–73), arginine (0.79) and tyrosine (0.63) followed by alanine (0.54), proline (0.47) and serine (0–37). Hepatic removal of AA-N exceeded the increase in urea-N formation such that, at the highest rate of infusion, approximately 10 mmol/min of the extracted AA was apparently available for hepatic anabolism, more than is required to account for assumed increases in liver mass and export protein synthesis. Similarly, the amount of AA available for peripheral tissue protein gain, when assessed against phenylalanine supply as the limitation, would be the equivalent of a maximum of 0.5 g protein retained/min (6 mmol AA-N/min). This would provide sufficient AA for replenishment of peripheral (muscle) protein stores plus support of the placenta and fetus.

Type
Animal Nutrition
Copyright
Copyright © The Nutrition Society 1997

References

REFERENCES

Abbott, E. M., Parkins, J. J. & Holmes, P. H. (1985) Influence of dietary protein on the pathophysiology of ovine haemonchosis in Finn Dorset and Scottish Blackface lambs given a single moderate infection. Research in Veterinary Science 38, 5460.CrossRefGoogle Scholar
Bell, A. W. (1995) Regulation of organic nutrient metabolism during transition from late pregnancy to early lactation. Journal of Animal Science 73, 28042819.CrossRefGoogle ScholarPubMed
Bergman, E. N. (1973) Glucose metabolism in ruminants as related to hypoglycemia and ketosis. Cornell Veterinarian 63, 341382.Google Scholar
Brier, B. H., Gallagher, B. W. & Gluckman, P. D. (1991) Radioimmunoassay for insulin-like growth factor-1: solutions to some potential problems and pitfalls. Journal of Endocrinology 128, 347357.CrossRefGoogle Scholar
Burrin, D. G., Ferrell, C. L., Britton, R. A. & Bauer, M. (1990) Level of nutrition and visceral organ size and metabolic activity in sheep. British Journal of Nutrition 64, 439448.CrossRefGoogle ScholarPubMed
Christensen, H. N. (1990) Role of amino acid transport and countertransport in nutrition and metabolism. Physiological Reviews 70, 4377.CrossRefGoogle ScholarPubMed
Connell, A., Calder, A. G., Anderson, S. E. & Lobley, G. E. (1997) Hepatic protein synthesis in the sheep: effect of intake as monitored by use of stable-isotope-labelled glycine, leucine and phenylalanine. British Journal of Nutrition 77, 255271.CrossRefGoogle ScholarPubMed
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
Davis, T. D., Burrin, D. G., Fiorotto, M. L. & Nguyen, H. V. (1996) Protein synthesis in skeletal muscle and jejunum is more responsive to feeding in 7- than in 26-day-old pigs. American Journal of Physiology 270, E802E809.Google ScholarPubMed
Elwyn, D. H., Launder, W. J., Parikh, H. C. & Wise, E. M. Jr (1972) Roles of plasma and erythrocytes in interorgan transport of amino acids in dogs. American Journal of Physiology 222, 13331342.CrossRefGoogle ScholarPubMed
Hanigan, M. D., France, J., Wray-Cahen, D., Beever, D. E., Lobley, G. E., Reutzel, L. & Smith, N. E. (1998) Alternative models for analyses of liver and mammary transorgan metabolite extraction data. British Journal of Nutrition 79 (In the Press).CrossRefGoogle ScholarPubMed
Houlier, M. L., Patureau-Mirand, P., Durand, D., Bauchart, D., Lefaivre, J. & Bayle, A. (1991) Transport des acides amines dans l'aire splanchnic par le plasma sanguin et le sang chez le veau préruminant (Transport of amino acids in blood and plasma across the splanchnic region of preruminant calves). Reproduction, Nutrition and Development 31, 399410.CrossRefGoogle Scholar
Huntington, G. B., Reynolds, C. K. & Stroud, B. H. (1989) Techniques for measuring blood flow in splanchnic tissues of cattle. Journal of Dairy Science 72, 15831595.CrossRefGoogle ScholarPubMed
Lindsay, D. B. (1993). Metabolism of the portal-drained viscera. In Quantitative Aspects of Ruminant Digestion and Metabolism pp. 267289 ]Forbes, J.M. and France, J., editors[. Wallingford: CAB INTERNATIONAL.Google Scholar
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 AA catabolism. British Journal of Nutrition 73, 667685.CrossRefGoogle Scholar
Lobley, G. E., Connell, A., Revell, D. K., Bequette, 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
McGivan, J. D. (1992). Techniques used in the study of plasma membrane amino acid transport. In Mammalian Amino Acid Transport; Mechanisms and Control pp. 5163 ]Kilberg, M.S. and Haussinger, D., editors[. New York: Plenum Press.CrossRefGoogle Scholar
McGivan, J. D., Bradford, N. & Merdes-Mourao, J. (1977) The transport of branched-chain amino acids into isolated rat liver cells. FEBS Letters 80, 380394.CrossRefGoogle ScholarPubMed
Meijer, A. J., Lof, C., Ramos, I. C. & Verhoeven, A. J. (1985) Control of ureagenesis. European Journal of Biochemistry 148, 189196.CrossRefGoogle Scholar
Metcalf, J. A., Beever, D. E., Sutton, J. D., Wray-Cahen, D., Evans, R. T., Humphries, D. J., Backwell, F. R. C., Bequette, B. J. & MacRae, J. C. (1994) The effect of supplementary protein on in vivo metabolism of the mammary gland in lactating dairy cows. Journal of Dairy Science 77, 18161827.CrossRefGoogle ScholarPubMed
Mortimore, G. E. & Surmacz, C. A. (1984) Liver perfusion: an in vitro technique for the study of intracellular protein turnover and its regulation in vivo. Proceedings of the Nutrition Society 43, 161167.CrossRefGoogle Scholar
Mosoni, L., Houlier, M.-L., Mirand, P. P., Bayle, G. & Grizard, J. (1993) Effect of amino acids alone or with insulin on muscle and liver protein synthesis in adult and old rats. American Journal of Physiology 264, E614E620.Google ScholarPubMed
Pell, J. M., Calderone, E. M. & Bergman, E. N. (1986) Leucine and a-ketoisocaproate metabolism and interconversions in fed and fasted sheep. Metabolism 35, 10051016.CrossRefGoogle ScholarPubMed
Rérat, A., Simoes-Nuñes, C., Mendy, F., Vaissade, P. & Vaugelade, P. (1992) Splanchnic fluxes of amino acids after duodenal infusion of carbohydrate solutions containing free amino acids or oligopeptides in the non-anaesthetized pig. British Journal of Nutrition 68, 111138.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
Seal, C. J., Parker, D. S. & Avery, P. J. (1992) The effect of forage and forage-concentrate diets on rumen fermentation and metabolism of nutrients by the mesenteric- and portal-drained viscera in growing steers. British Journal of Nutrition 67, 355370.CrossRefGoogle ScholarPubMed
Sigaard-Anderson, O. (1974) The Acid-Base Status of Blood 4th revised ed., p. 22. Copenhagen: Munksgaard.Google Scholar
Symonds, M. E., Bryant, M. J. & Lomax, M. A. (1986) The effect of shearing on the energy metabolism of the pregnant ewe. British Journal of Nutrition 56, 635643.CrossRefGoogle ScholarPubMed
Tauveron, I., Larbaud, D., Champredon, C., Debras, E., Tesseraud, S., Bayle, G., Bonnet, Y., Thieblot, P. & Grizard, J. (1994) Effect of hyperinsulinemia and hyperaminoacidemia on muscle and liver protein synthesis in lactating goats. American Journal of Physiology 267, E877E885.Google ScholarPubMed
Tindall, J. S., Knaggs, G. S., Hart, I. C. & Blake, L. A. (1978) Release of growth hormone in lactating and non-lactating goats in relation to behaviour, stages of sleep, electroencephalograms, environmental stimuli and levels of prolactin, insulin, glucose and free fatty acids in the circulation. Journal of Endocrinology 76, 333346.CrossRefGoogle Scholar
Wolff, J. E. & Bergman, E. N. (1972) Metabolism and interconversions of five plasma amino acids by tissues of the sheep. American Journal of Physiology 223, 447454.CrossRefGoogle ScholarPubMed
Wolff, J. E., Bergman, E. N. & Williams, H. H. (1972) Net metabolism of plasma amino acids by liver and portal-drained viscera of fed sheep. American Journal of Physiology 223, 438446.CrossRefGoogle ScholarPubMed