Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-11-08T09:20:24.528Z Has data issue: false hasContentIssue false

Ketogenesis in the liver of ruminants – adaptations to a challenge

Published online by Cambridge University Press:  27 March 2009

V. A. Zammit
Affiliation:
Hannah Research Institute, Ayr, Scotland, KA6 5HL, UK

Extract

The descriptive aspects of hepatic fatty acid metabolism, and of ketogenesis in particular, have been extensively described for ruminants. There is, however, a distinct lack of information on the more mechanistic aspects of the subject. The biochemical profile of the livers of ruminant species shows both similarities to, and striking differences from, that of simple-stomached animals. Consequently, it may not always be valid to extrapolate from the situation in, say, rat liver to that in ruminant liver in order to interpret experimental observations in ruminants. Of perhaps greater interest is the recognition that the adaptations in the ruminant system are important not only in enabling us to rationalize the physiological changes observed in ruminants, but are in themselves of interest in the analysis of metabolic regulatory strategies. Consequently, this review deals with the peculiarities of the regulation of hepatic ketogenesis in ruminants, and the biochemical mechanisms that may explain their existence.

Type
Review
Copyright
Copyright © Cambridge University Press 1990

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

Aiello, R. J., Kenna, T. M. & Herbein, J. H. (1984). Hepatic gluconeogenic and ketogenic inter-relationships in the lactating cow. Journal of Dairy Science 67, 17071714.CrossRefGoogle 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(-)-β-hydroxybutyrate, palmitate, oleate and stearate, and rates of production and oxidation of propionate and butyrate in fed and starved sheep. Biochemical Journal 104, 135144.CrossRefGoogle ScholarPubMed
Baird, D. G. (1977). Aspects of ruminant intermediary metabolism in relation to ketosis. Biochemical Society Transactions 5, 819827.CrossRefGoogle ScholarPubMed
Baird, D. G. (1982). Primary ketosis in the high-producing dairy cow: clinical and subclinical disorders, treatment, prevention and outlook. Journal of Dairy Science 65, 110.CrossRefGoogle ScholarPubMed
Baird, D. G., Heitzman, R. J., Reid, I. M., Symonds, H. W. & Lomax, M. A. (1979). Effects of food deprivation on ketonaemia, ketogenesis and hepatic intermediary metabolism in the non-lactating dairy cow. Biochemical Journal 178, 3544.CrossRefGoogle ScholarPubMed
Bergman, E. N. (1968). Glycerol turnover in the nonpregnant and ketotic pregnant sheep. American Journal of Physiology 215, 865873.CrossRefGoogle ScholarPubMed
Brindle, N. P. J. (1985). Comparative studies on the regulation of hepatic fatty acid metabolism. PhD thesis, University of Manchester.Google Scholar
Brindle, N. P. J., Zammit, V. A. & Pogson, C. I. (1985 a). Regulation of carnitine palmitoyltransferase activity by malonyl-CoA in mitochondria from sheep liver, a tissue with a low capacity for fatty acid synthesis. Biochemical Journal 232, 177182.CrossRefGoogle ScholarPubMed
Brindle, N. P., Zammit, J., A., V. & Pogson, C. I. (1985 b). Inhibition of sheep liver carnitine palmitoyltransferase by methylmalonyl-CoA. Biochemical Society Transactions 13, 880881CrossRefGoogle Scholar
Bush, R. S. & Milligan, L. P. (1971). Study of the mechanism of inhibition of ketogenesis by propionate in bovine liver. Canadian Journal of Animal Science 51, 121127.CrossRefGoogle Scholar
Faulkner, A. & Pollock, H. T. (1986). Propionate metabolism and its regulation by fatty acids in ovine hepatocytes. Comparative Biochemistry and Physiology 84B, 559563.Google Scholar
Faulkner, A. & Pollock, H. T. (1988). Inter-regulation of volatile and long-chain fatty acid metabolism in ovine hepatocytes. Biochemical Society Transactions 16, 203204.CrossRefGoogle Scholar
Grantham, B. D. & Zammit, V. A. (1986). Restoration of the properties of carnitine palmitoyltransferase I in liver mitochondria during refeeding of starved rats. Biochemical Journal 239, 485488.CrossRefGoogle ScholarPubMed
Grantham, B. D. & Zammit, V. A. (1988). Role of carnitine palmitoyltransferase I in the regulation of hepatic ketogenesis during the onset and reversal of chronic diabetes. Biochemical Journal 249, 409414.CrossRefGoogle ScholarPubMed
Ingle, D. L., Bauman, D. G. & Carvigus, U. S. (1972). Lipogenesis in the ruminant: in vitro site of fatty acid synthesis in sheep. Journal of Nutrition 102, 617624.CrossRefGoogle Scholar
Klepp, B. B., Aiello, R. J., Grummer, R. R. & Armentano, L. E. (1988). Triglyceride accumulation and very low density lipoprotein secretion by rat and goat hepatocytes in vitro. Journal of Dairy Science 71, 18131818.CrossRefGoogle Scholar
Koundakjian, P. P. & Snoswell, A. M. (1970). Ketone body and fatty acid metabolism in sheep tissues. 3-Hydroxybutyrate dehydrogenase, a cytoplasmic enzyme in sheep liver and kidney. Biochemical Journal 119, 4957.CrossRefGoogle ScholarPubMed
Krebs, H. A. (1966). Bovine ketosis. Veterinary Record 78, 187192.CrossRefGoogle Scholar
Kronfeld, D. S. (1969). Excess gluconeogenesis and oxaloacetate depletion in bovine ketosis. Nutrition Reviews 27, 131133.CrossRefGoogle Scholar
Lomax, M. A., Donaldson, I. A. & Pogson, C. I. (1983). The control of fatty acid metabolism in liver cells from fed and starved sheep. Biochemical Journal 214, 553560.CrossRefGoogle ScholarPubMed
Lowe, D. M. & Tubbs, P. K. (1985). Succinylation and inactivation of 3-hydroxy-3-methyl glutaryl-CoA synthase by succinyl-CoA and its possible relevance to the control of ketogenesis. Biochemical Journal 232, 3742.CrossRefGoogle Scholar
Mcgarry, J. D. & Foster, D. W. (1980). Regulation of hepatic fatty acid oxidation and ketone body production. Annual Review of Biochemistry 49, 395420.CrossRefGoogle ScholarPubMed
Nielson, N. C. & Fleischer, S. (1970). β-Hydroxybutyrate dehydrogenase: lack in ruminant liver mitochondria. Science 166, 10171019.CrossRefGoogle Scholar
Paradies, G. & Papa, S. (1975). The transport of mocarboxylic oxoacids in rat liver mitochondria. FEBS Letters 52, 149152.CrossRefGoogle ScholarPubMed
Radloff, H. D. & Schultz, L. H. (1967). Blood and rumen changes in cows in early stages of ketosis. Journal of Dairy Science 50, 6872.CrossRefGoogle Scholar
Snoswell, A. M. & Henderson, G. D. (1970). Aspects of carnitine ester metabolism in sheep liver. Biochemical Journal 119, 5965.CrossRefGoogle ScholarPubMed
Snoswell, A. M. & Henderson, G. D. (1980). Carnitine and metabolism in ruminant animals. In Carnitine Biosynthesis, Metabolism and Functions (Eds Frenkel, R. A. & McGarry, J. D.), pp. 191205. New York: Academic Press.CrossRefGoogle Scholar
Varnam, G., Jeacock, M. & Shepherd, D. (1978). Hepatic ketone-body metabolism in developing sheep and pregnant ewes. British Journal of Nutrition 40, 359367.CrossRefGoogle ScholarPubMed
Williamson, D. H. & Kuenzel, P. (1971). The nature of the ‘cytoplasmic 3-hydroxybutyrate dehydrogenase’ from sheep kidney. Biochemical Journal 178, 3544.Google Scholar
Zammit, V. A., (1984). Mechanisms of regulation of the partition of fatty acids between oxidation and esterification in the liver. Progress in Lipid Research 23, 3967.CrossRefGoogle ScholarPubMed
Zammit, V. A., Corstorphine, C. G. & Kelliher, M. G. (1988). Evidence for distinct functional molecular sizes of carnitine palmitoyltransferases I and II in rat liver mitochondria. Biochemical Journal 250, 415420.CrossRefGoogle Scholar
Zammit, V. A., Corstorphine, C. G. & Kolodziei, M. P. (1989). Target size analysis by radiation inactivation of carnitine palmitoyltransferase activity and malonyl-CoA binding in outer membranes from rat liver mitochondria. Biochemical Journal 263, 8995.CrossRefGoogle ScholarPubMed