Hostname: page-component-848d4c4894-r5zm4 Total loading time: 0 Render date: 2024-06-22T14:55:11.821Z Has data issue: false hasContentIssue false

Some observations on metabolite production and utilization in vivo by the gut and liver of adult dairy cows

Published online by Cambridge University Press:  27 March 2009

G. D. Baird
Affiliation:
Departments of Biochemistry and Functional Pathology, Agricultural Research Council, Institute for Research on Animal Diseases, Compton, Berks., U.K. R616 ONN
H. W. Symonds
Affiliation:
Departments of Biochemistry and Functional Pathology, Agricultural Research Council, Institute for Research on Animal Diseases, Compton, Berks., U.K. R616 ONN
R. Ash
Affiliation:
Departments of Biochemistry and Functional Pathology, Agricultural Research Council, Institute for Research on Animal Diseases, Compton, Berks., U.K. R616 ONN

Summary

Metabolite production rates were determined in the portal vein and hepatic veins of catheterized adult dairy cows maintained under normal conditions of husbandry. The production rates were calculated from the metabolite concentrations in arterial, portal and hepatic-venous blood, and from the rates of blood flow in the portal vein and the hepatic veins. In general, qualitatively similar metabolite production was observed in three non-lactating and two lactating cows, but production rates tended to be higher in the lactating cows due to higher blood flow rates.

About half the lactate utilized by the liver was absorbed from the gut, while the other half was derived from endogenous sources. Lactate absorbed from the gut was quantitatively of less significance than propionate as a substrate for hepatic metabolism. Even in cows that were well fed, there was a net production of ketone bodies from the liver that was almost as great as the net production from the gut. However, while the liver produced D-3-hydroxybutyrate it took up acetoacetate. In the lactating cows, acetate, propionate and butyrate were absorbed from the gut in the proportions of 9·5:2·5:1, respectively. About 90% and 80% of the absorbed propionate and butyrate, respectively, were taken up by the liver.

On the routine hay/concentrate diet there was little net uptake or output of glucose by the gut. However, there was consistent production of glucose by the liver, amounting to a maximum, in this study, of about 11 mol/24 h, assuming constant glucose production throughout the 24 h day. The rate of carbon dioxide appearance in the portal vein was about twice that of oxygen uptake by the gut. The liver used oxygen, and produced carbon dioxide, at nearly equal rates. The uptake of glucogenic substrates by the liver accounted adequately for the observed rates of hepatic gluconeogenesis.

In one of the lactating cows it was observed that there was a net production of acetate by the liver that amounted to half the net absorption of acetate from the gut (ethyl alcohol was not the precursor of this acetate) and that (glutamine + asparagine) and serine had the highest rates of appearance in the portal vein and the highest rates of uptake by the liver.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1975

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Annison, E. F. & Armstrong, D. G. (1970). Volatile fatty acid metabolism and energy supply. In Physiology of Digestion and Metabolism in the Ruminant (ed. Phillipson, A. T.), pp. 422–37. Newcastle-upon-Tyne: Oriel Press.Google Scholar
Annison, E. F., Brown, R. E., Leng, R. A., Lindsay, D. B. & West, C. E. (1967). Rates of entry and oxidation of acetate, glucose, D(–)--hydroxybutyrate, palmitate, oleate and stearate, and rates of production and oxidation of propionate and butyrate, in fed and starved sheep. Biochemical Journal 104, 135–47.CrossRefGoogle Scholar
Ash, R. & Baird, G. D. (1973). Activation of volatile fatty acids in bovine liver and rumen epithelium. Evidence for control by autoregulation. Biochemical Journal 136, 311–19.CrossRefGoogle ScholarPubMed
Baird, G. D. & Heitzman, R. J. (1970). Gluconeogenesis in the cow. The effects of a glucocorticoid on hepatic intermediary metabolism. Biochemical Journal 116, 865–74.CrossRefGoogle ScholarPubMed
Baird, G. D., Symonds, H. W. & Ash, R. (1974). Determination of portal and hepatic metabolite production rates in the adult dairy cow. Proceedings of the Nutrition Society 33, 70A71A.Google ScholarPubMed
Bensadoun, A. & Reid, J. T. (1962). Estimation of rate of portal blood flow in ruminants: effect of feeding, fasting and anesthesia. Journal of Dairy Science 45, 540–43.CrossRefGoogle Scholar
Bergman, E. N. (1973). Glucose metabolism in ruminants as related to hypoglycemia and ketosis. Cornell Veterinarian 63, 431–82.Google Scholar
Bergman, E. N. & Wolff, J. E. (1971). Metabolism of volatile fatty acids by liver and portal-drained viscera of sheep. American Journal of Physiology 221, 586–92.CrossRefGoogle Scholar
Bickerstaffe, R., Annison, E. F. & Linzell, J. L. (1974). The metabolism of glucose, acetate, lipids and amino acids in lactating dairy cows. Journal of Agricultural Science, Cambridge 82, 7185.CrossRefGoogle Scholar
Blaxter, K. L. (1967). The Energy Metabolism of Ruminants, pp. 252–5. London: Hutchinson.Google Scholar
Bock, A. V., Field, H. & Adair, G. S. (1924). The oxygen and carbon dioxide dissociation curves of human blood. Journal of Biological Chemistry 59, 353–78.CrossRefGoogle Scholar
Bradley, S. E., Ingelfinger, F. J., Bradley, G. P. & Curry, J. J. (1945). The estimation of hepatic blood flow in man. Journal of Clinical Investigation 24, 890–7.CrossRefGoogle ScholarPubMed
Cook, R. M. & Miller, L. D. (1965). Utilization of volatile fatty acids in ruminants. 1. Removal of them from portal blood by the liver. Journal of Dairy Science 48, 1339–45.CrossRefGoogle Scholar
Harrison, F. A. (1969). The introduction and maintenance of permanently indwelling catheters in the portal and hepatic veins of the sheep. Journal of Physiology 200, 28P30P.Google ScholarPubMed
Harrison, F. A., Linzell, J. L. & Paterson, J. Y. F. (1971). Oxygen consumption by the liver of the conscious sheep. Journal of Physiology, 222, 48P49P.Google Scholar
Katz, M. L. & Bergman, E. N. (1969a). Simultaneous measurements of hepatic and portal venous blood flow in the sheep and dog. American Journal of Physiology 216, 946–52.CrossRefGoogle ScholarPubMed
Katz, M. L. & Bergman, E. N. (1969b). Hepatic and portal metabolism of glucose, free fatty acids and ketone bodies in sheep. American Journal of Physiology 216, 953–60.CrossRefGoogle Scholar
Koundakjian, P. P. & Snoswell, A. M. (1970). Ketone body and fatty acid metabolism in sheep tissues. 3-Hydroxybutyrate dehydrogenase, acytoplasmic enzyme in sheep liver and kidney. Biochemical Journal 119, 4957.CrossRefGoogle Scholar
Krebs, H. A. & Perkins, J. R. (1970). The physiological role of liver alcohol dehydrogenase. Biochemical Journal 118, 635–44.CrossRefGoogle ScholarPubMed
Leng, R. A., Steel, J. W. & Luick, J. R. (1967). Contribution of propionate to glucose synthesis in sheep. Biochemical Journal 103, 785–90.CrossRefGoogle ScholarPubMed
Palmqtjist, D. L. (1972). Palmitic acid as a source of endogenous acetate and β-hydroxybutyrate in fed and fasted ruminants. Journal of Nutrition 102, 1401–6.CrossRefGoogle Scholar
Pennington, R. J. (1952). The metabolism of shortchain fatty acids in the sheep. 1. Fatty acid utilization and ketone body production by rumen epithelium and other tissues. Biochemical Journal 51, 251–8.CrossRefGoogle Scholar
Pennington, R. J. & Sutherland, T. M. (1956). The metabolism of short-chain fatty acids in the sheep. 4. The pathway of propionate metabolism in rumen epithelium tissue. Biochemical Journal 63, 618–28.CrossRefGoogle Scholar
Scrtttton, M. C. & Utter, M. F. (1968). The regulation of glycolysis and gluconeogenesis in animal tissues. Annual Review of Biochemistry 37, 249302.CrossRefGoogle Scholar
Settfert, C. D., Graf, M., Janson, G., Kuhn, A. & Soling, H. D. (1974). Formation of free acetate by isolated perfused livers from normal, starved and diabetic rats. Biochemical and Biophysical Research Communications 57, 901–9.Google Scholar
Shoemaker, W. C. (1960). Measurement of hepatic blood flow in the unanesthetized dog by a modified bromosulphalein method. Journal of Applied Physiology 15, 473–8.CrossRefGoogle Scholar
Slein, M. W. (1963). D-Glucose. Determination with hexokinase and glucose-6-phosphate dehydrogenase. In Methods of Enzymatic Analysis (ed. Bergmeyer, H. U.), pp. 117–23. London: Academic Press.Google Scholar
Symonds, H. W. & Baird, G. D. (1973). Cannulation of an hepatic vein, the portal vein and a mesenteric vein in the cow, and its use in the measurement of blood flow rates. Research in Veterinary Science 14, 267–9.CrossRefGoogle Scholar
Symonds, H. W. & Baird, G. D. (1975). Evidence for the absorption of reducing sugar from the small intestine of the dairy cow. British Veterinary Journal 131, 1722.CrossRefGoogle ScholarPubMed
Waldern, D. E., Johnson, V. L. & Blossek, T. H. (1963). Cardiac output in the bovine and its relationship to rumen and portal volatile fatty acid concentration. Journal of Dairy Science 46, 327–32.CrossRefGoogle Scholar
Watson, H. R. & Lindsay, D. B. (1972). 3-Hydroxybutyrate dehydrogenase in tissues from normal and ketonaemic sheep. Biochemical Journal 128, 53–7.CrossRefGoogle ScholarPubMed
Weast, R. C. (1971). Handbook of Chemistry and Physics 52nd ed.Cleveland, Ohio: Chemical Rubber Co.Google Scholar
Weekes, T. E. C. & Webster, A. J. F. (1974). Metabolism of propionate by the portal-drained viscera of sheep. Proceedings of the Nutrition Society 33, 71A–72A.Google Scholar
Weigand, E., Young, J. W. & McGilliard, A. D. (1972). Extent of propionate metabolism during absorption from the bovine rumino-reticulum. Biochemical Journal 126, 201–9.CrossRefGoogle Scholar
Wiltrout, D. W. & Satter, L. D. (1972). Contribution of propionate to glucose synthesis in the lactating and non-lactating cow. Journal of Dairy Science 55, 307–17.CrossRefGoogle Scholar
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, 438–46.CrossRefGoogle ScholarPubMed