Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1970 Apr;117(2):231–235. doi: 10.1042/bj1170231

Adenine nucleotides and the adenylate kinase equilibrium in livers of foetal and newborn rats

F J Ballard 1
PMCID: PMC1178854  PMID: 5420030

Abstract

1. Measurements of ATP, ADP and AMP concentrations in livers of rats that had been delivered by Caesarian section indicate a rapid shift from a low to a high [ATP]/[AMP] ratio. This change is consistent with the cessation of glycolysis and the initiation of gluconeogenesis at birth. 2. When newborn animals are exposed to a 100% nitrogen atmosphere the hepatic ATP concentration falls and AMP increases. 3. Calculations of the [ATP][AMP]/[ADP]2 ratio give values that are close to the equilibrium constant of adenylate kinase except when the ATP concentration is high. 4. This difference cannot be accounted for by the preferential binding of available Mg2+ to ATP4− rather than ADP3−. It is concluded that the relative proportions of adenine nucleotides at any level of phosphorylation are only partly regulated by adenylate kinase.

Full text

PDF
231

Selected References

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

  1. Adelman R. C., Lo C. H., Weinhouse S. Dietary and hormonal effects on adenosine triphosphate: adenosine monophosphate phosphotransferase activity in rat liver. J Biol Chem. 1968 May 25;243(10):2538–2544. [PubMed] [Google Scholar]
  2. Atkinson D. E. Biological feedback control at the molecular level. Science. 1965 Nov 12;150(3698):851–857. doi: 10.1126/science.150.3698.851. [DOI] [PubMed] [Google Scholar]
  3. Atkinson D. E., Walton G. M. Adenosine triphosphate conservation in metabolic regulation. Rat liver citrate cleavage enzyme. J Biol Chem. 1967 Jul 10;242(13):3239–3241. [PubMed] [Google Scholar]
  4. 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]
  5. 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]
  6. Ballard F. J., Hanson R. W. Changes in lipid synthesis in rat liver during development. Biochem J. 1967 Mar;102(3):952–958. doi: 10.1042/bj1020952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. 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]
  8. 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]
  9. Dawkins M. J. Biochemical aspects of developing function in newborn mammalian liver. Br Med Bull. 1966 Jan;22(1):27–33. doi: 10.1093/oxfordjournals.bmb.a070432. [DOI] [PubMed] [Google Scholar]
  10. Goldberg N. D., Passonneau J. V., Lowry O. H. Effects of changes in brain metabolism on the levels of citric acid cycle intermediates. J Biol Chem. 1966 Sep 10;241(17):3997–4003. [PubMed] [Google Scholar]
  11. Heldt H. W., Schwalbach K. The participation of GTP-AMP-P transferase in substrate level phosphate transfer of rat liver mitochondria. Eur J Biochem. 1967 Apr;1(2):199–206. doi: 10.1007/978-3-662-25813-2_31. [DOI] [PubMed] [Google Scholar]
  12. KEECH D. B., UTTER M. F. PYRUVATE CARBOXYLASE. II. PROPERTIES. J Biol Chem. 1963 Aug;238:2609–2614. [PubMed] [Google Scholar]
  13. Markland F. S., Wadkins C. L. Adenosine triphosphate-adenosine 5'-monophosphate phosphotransferase of bovine liver mitochondria. II. General kinetic and structural properties. J Biol Chem. 1966 Sep 25;241(18):4136–4145. [PubMed] [Google Scholar]
  14. Metcalfe J., Bartels H., Moll W. Gas exchange in the pregnant uterus. Physiol Rev. 1967 Oct;47(4):782–838. doi: 10.1152/physrev.1967.47.4.782. [DOI] [PubMed] [Google Scholar]
  15. Morrison J. F., James E. The mechanism of the reaction catalysed by adenosine triphosphate-creatine phosphotransferase. Biochem J. 1965 Oct;97(1):37–52. doi: 10.1042/bj0970037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. 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]
  17. WOLLENBERGER A., RISTAU O., SCHOFFA G. [A simple technic for extremely rapid freezing of large pieces of tissue]. Pflugers Arch Gesamte Physiol Menschen Tiere. 1960;270:399–412. [PubMed] [Google Scholar]
  18. Williamson J. R., Olson M. S., Herczeg B. E., Coles H. S. Control of citrate formation in rat liver mitochondria. Biochem Biophys Res Commun. 1967 Jun 9;27(5):595–600. doi: 10.1016/s0006-291x(67)80029-9. [DOI] [PubMed] [Google Scholar]

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

RESOURCES