Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1970 Nov;120(2):385–392. doi: 10.1042/bj1200385

The development of gluconeogenesis in rat liver. Effects of glucagon and ether

Helen Philippidis 1, F J Ballard 1,*
PMCID: PMC1179609  PMID: 5493860

Abstract

1. Administration of glucagon to foetal rats produced a 10–15-fold increase in hepatic phosphoenolpyruvate carboxykinase activity together with a similar increase in the overall pathway of pyruvate conversion into glycogen in liver slices. 2. Glucagon was without effect on gluconeogenesis in vivo, which remained at approx. 0.1% of the incorporation as measured in newborn animals. 3. The apparent discrepancy between these results was due to the ether anaesthesia that was required for experimentation in vivo. Under conditions when minimal ether was used, the rates of labelling of glycogen from [3-14C]pyruvate in vivo were increased 10–20-fold and there was an additional stimulus by glucagon. 4. Ether anaesthesia produced a more reduced redox state of the foetal liver cytosol and lowered the ATP/ADP concentration ratio. 5. It is proposed that these effects are significant in the limitation of gluconeogenesis in the foetal rat liver, so that only with high phosphoenolpyruvate carboxykinase activity, high ATP concentration and a relatively oxidized cytosol redox state will a functional gluconeogenic pathway be present.

Full text

PDF
385

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BALLARD F. J., OLIVER I. T. CARBOHYDRATE METABOLISM IN LIVER FROM FOETAL AND NEONATAL SHEEP. Biochem J. 1965 Apr;95:191–200. doi: 10.1042/bj0950191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BALLARD F. J., OLIVER I. T. Glycogen metabolism in embryonic chick and neonatal rat liver. Biochim Biophys Acta. 1963 Jun 4;71:578–588. doi: 10.1016/0006-3002(63)91130-2. [DOI] [PubMed] [Google Scholar]
  3. Ballard F. J., Hanson R. W. Phosphoenolpyruvate carboxykinase and pyruvate carboxylase in developing rat liver. Biochem J. 1967 Sep;104(3):866–871. doi: 10.1042/bj1040866. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chang H. C., Lane M. D. The enzymatic carboxylation of phosphoenolpyruvate. II. Purification and properties of liver mitochondrial phosphoenolpyruvate carboxykinase. J Biol Chem. 1966 May 25;241(10):2413–2420. [PubMed] [Google Scholar]
  5. Chang H. C., Maruyama H., Miller R. S., Lane M. D. The enzymatic carboxylation of phosphoenolpyruvate. 3. Investigation of the kinetics and mechanism of the mitochondrial phosphoenolpyruvate carboxykinase-catalyzed reaction. J Biol Chem. 1966 May 25;241(10):2421–2430. [PubMed] [Google Scholar]
  6. Exton J. H., Park C. R. Control of gluconeogenesis in liver. II. Effects of glucagon, catecholamines, and adenosine 3',5'-monophosphate on gluconeogenesis in the perfused rat liver. J Biol Chem. 1968 Aug 25;243(16):4189–4196. [PubMed] [Google Scholar]
  7. Exton J. H., Park C. R. The stimulation of gluconeogenesis from lactate by epinephrine, glucagon, cyclic 3',5'-adenylate in the perfused rat liver. Pharmacol Rev. 1966 Mar;18(1):181–188. [PubMed] [Google Scholar]
  8. Friedmann B., Goodman E. H., Jr, Weinhouse S. Dietary and hormonal effects on gluconeogenesis in the rat. J Biol Chem. 1965 Oct;240(10):3729–3735. [PubMed] [Google Scholar]
  9. Greengard O., Dewey H. K. Initiation by glucagon of the premature development of tyrosine aminotransferase, serine dehydratase, and glucose-6-phosphatase in fetal rat liver. J Biol Chem. 1967 Jun 25;242(12):2986–2991. [PubMed] [Google Scholar]
  10. HORNBROOK K. R., BURCH H. B., LOWRY O. H. CHANGES IN SUBSTRATE LEVELS IN LIVER DURING GLYCOGEN SYNTHESIS INDUCED BY LACTATE AND HYDROCORTISONE. Biochem Biophys Res Commun. 1965 Jan 18;18:206–211. doi: 10.1016/0006-291x(65)90741-2. [DOI] [PubMed] [Google Scholar]
  11. Philippidis H., Ballard F. J. The development of gluconeogenesis in rat liver: experiments in vivo. Biochem J. 1969 Jul;113(4):651–657. doi: 10.1042/bj1130651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Reade P. C., Jenkin C. R. The functional development of the reticulo-endothelial system. I. The uptake of intravenously injected particles by foetal rats. Immunology. 1965 Jul;9(1):53–60. [PMC free article] [PubMed] [Google Scholar]
  13. Veneziale C. M., Walter P., Kneer N., Lardy H. A. Influence of L-tryptophan and its metabolites on gluconeogenesis in the isolated, perfused liver. Biochemistry. 1967 Jul;6(7):2129–2138. doi: 10.1021/bi00859a034. [DOI] [PubMed] [Google Scholar]
  14. Williamson D. H., Lund P., Krebs H. A. The redox state of free nicotinamide-adenine dinucleotide in the cytoplasm and mitochondria of rat liver. Biochem J. 1967 May;103(2):514–527. doi: 10.1042/bj1030514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Williamson J. R., Browning E. T., Scholz R. Control mechanisms of gluconeogenesis and ketogenesis. I. Effects of oleate on gluconeogenesis in perfused rat liver. J Biol Chem. 1969 Sep 10;244(17):4607–4616. [PubMed] [Google Scholar]
  16. Williamson J. R., Browning E. T., Scholz R., Kreisberg R. A., Fritz I. B. Inhibition of fatty acid stimulation of gluconeogenesis by (+)-decanoylcarnitine in perfused rat liver. Diabetes. 1968 Apr;17(4):194–208. doi: 10.2337/diab.17.4.194. [DOI] [PubMed] [Google Scholar]
  17. Yeung D., Oliver I. T. Factors affecting the premature induction of phosphopyruvate carboxylase in neonatal rat liver. Biochem J. 1968 Jun;108(2):325–331. doi: 10.1042/bj1080325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Yeung D., Oliver I. T. Gluconeogenesis from amino acids in neonatal rat liver. Biochem J. 1967 Jun;103(3):744–748. doi: 10.1042/bj1030744. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES