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. 1983 Aug 15;214(2):525–532. doi: 10.1042/bj2140525

Postnatal hypoglycaemia and gluconeogenesis in the newborn rat. Delayed onset of gluconeogenesis in prematurely delivered newborns.

E Fernández, C Valcarce, J M Cuezva, J M Medina
PMCID: PMC1152276  PMID: 6615479

Abstract

The concentrations of glucose and lactate in the blood and of liver glycogen, and the phosphoenolpyruvate carboxykinase activity in liver and kidney of term and preterm newborn rats, were studied during the first 6 h post partum. Rates of lactate turnover and gluconeogenesis in vivo from [U-14C]lactate at 3 h and 6 h post partum were also quantified. The development of the prolonged postnatal hypoglycaemia observed after birth in the premature newborn rat is associated with lower rates of glucose production through glycogenolysis and gluconeogenesis; liver glycogenolysis was the main contributing factor to the glucose available during the neonatal period studied in both groups. Delayed induction of liver phosphoenolpyruvate carboxykinase activity was observed in premature newborn rats. Renal phosphoenolpyruvate carboxykinase activity increased 72% from birth in preterm newborns, but only a 25% increase was found in term newborns during the same experimental period. The gluconeogenesis in vivo from [U-14C]lactate paralleled the appearance of cytosolic phosphoenolpyruvate carboxykinase activity in the liver of both groups of newborns. Blood lactate concentrations remained higher in preterm than in term newborns. The postnatal utilization of lactate via the gluconeogenic pathway in either group of newborns was always less than 20% of the total lactate used. The results presented are discussed in relation to the development of postnatal hypoglycaemia and gluconeogenesis in the premature newborn rat.

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Selected References

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

  1. 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]
  2. Ballard F. J. The development of gluconeogenesis in rat liver. Controlling factors in the newborn. Biochem J. 1971 Sep;124(2):265–274. doi: 10.1042/bj1240265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bashan N., Gross Y., Moses S., Gutman A. Rat liver glycogen metabolism in the perinatal period. Biochim Biophys Acta. 1979 Oct 4;587(2):145–154. doi: 10.1016/0304-4165(79)90349-0. [DOI] [PubMed] [Google Scholar]
  4. Beard A., Cornblath M., Gentz J., Kellum M., Persson B., Zetterström R., Haworth J. C. Neonatal hypoglycemia: a discussion. J Pediatr. 1971 Aug;79(2):314–324. doi: 10.1016/s0022-3476(71)80123-3. [DOI] [PubMed] [Google Scholar]
  5. Cake M. H., Yeung D., Oliver I. T. The control of postnatal hypoglycemia. Suggestions based on experimental observations in neonatal rats. Biol Neonate. 1971;18(3):183–192. doi: 10.1159/000240361. [DOI] [PubMed] [Google Scholar]
  6. Cuezva J. M., Burkett E. S., Kerr D. S., Rodman H. M., Patel M. S. The newborn of diabetic rat. I. Hormonal and metabolic changes in the postnatal period. Pediatr Res. 1982 Aug;16(8):632–637. doi: 10.1203/00006450-198208000-00009. [DOI] [PubMed] [Google Scholar]
  7. Cuezva J. M., Chitra C. I., Patel M. S. The newborn of diabetic rat. II. Impaired gluconeogenesis in the postnatal period. Pediatr Res. 1982 Aug;16(8):638–643. doi: 10.1203/00006450-198208000-00010. [DOI] [PubMed] [Google Scholar]
  8. Cuezva J. M., Moreno F. J., Medina J. M., Mayor F. Prematurity in the rat. I. Fuels and gluconeogenic enzymes. Biol Neonate. 1980;37(1-2):88–95. doi: 10.1159/000241260. [DOI] [PubMed] [Google Scholar]
  9. Di Marco P. N., Ghisalberti A. V., Martin C. E., Oliver I. T. Perinatal changes in liver corticosterone, serum insulin and plasma glucagon and corticosterone in the rat. Eur J Biochem. 1978 Jun 15;87(2):243–247. doi: 10.1111/j.1432-1033.1978.tb12372.x. [DOI] [PubMed] [Google Scholar]
  10. Di Marco P. N., Oliver I. T. Adenosine 3':5'-monophosphate in perinatal rat liver. Ontogeny and response to hormones. Eur J Biochem. 1978 Jun 15;87(2):235–241. doi: 10.1111/j.1432-1033.1978.tb12371.x. [DOI] [PubMed] [Google Scholar]
  11. Girard J. R., Cuendet G. S., Marliss E. B., Kervran A., Rieutort M., Assan R. Fuels, hormones, and liver metabolism at term and during the early postnatal period in the rat. J Clin Invest. 1973 Dec;52(12):3190–3200. doi: 10.1172/JCI107519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Girard J. R., Guillet I. Glucose turnover rate in newborn rats. Biochem J. 1975 May;148(2):345–347. doi: 10.1042/bj1480345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gregoire N. M., Gjedde A., Plum F., Duffy T. E. Cerebral blood flow and cerebral metabolic rates for oxygen, glucose, and ketone bodies in newborn dogs. J Neurochem. 1978 Jan;30(1):63–69. doi: 10.1111/j.1471-4159.1978.tb07035.x. [DOI] [PubMed] [Google Scholar]
  14. Gutberlet R. L., Cornblath M. Neonatal hypoglycemia revisited, 1975. Pediatrics. 1976 Jul;58(1):10–17. [PubMed] [Google Scholar]
  15. Hanson R. W., Ballard J. Hormonal regulation of hepatic P-enolpyruvate carboxykinase (GTP) during development. Fed Proc. 1975 Feb;34(2):166–171. [PubMed] [Google Scholar]
  16. Hawkins R. A., Williamson D. H., Krebs H. A. Ketone-body utilization by adult and suckling rat brain in vivo. Biochem J. 1971 Mar;122(1):13–18. doi: 10.1042/bj1220013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hellmann J., Vannucci R. C., Nardis E. E. Blood-brain barrier permeability to lactic acid in the newborn dog: lactate as a cerebral metabolic fuel. Pediatr Res. 1982 Jan;16(1):40–44. doi: 10.1203/00006450-198201001-00008. [DOI] [PubMed] [Google Scholar]
  18. Iynedjian P. B., Ballard F. J., Hanson R. W. The regulation of phosphoenolpyruvate carboxykinase (GTP) synthesis in rat kidney cortex. The role of acid-base balance and glucocorticoids. J Biol Chem. 1975 Jul 25;250(14):5596–5603. [PubMed] [Google Scholar]
  19. Lubchenco L. O., Bard H. Incidence of hypoglycemia in newborn infants classified by birth weight and gestational age. Pediatrics. 1971 May;47(5):831–838. [PubMed] [Google Scholar]
  20. Martín A., Caldés T., Benito M., Medina J. M. Regulation of glycogenolysis in the liver of the newborn rat in vivo. Inhibitory effect of glucose. Biochim Biophys Acta. 1981 Feb 5;672(3):262–267. doi: 10.1016/0304-4165(81)90292-0. [DOI] [PubMed] [Google Scholar]
  21. Medina J. M., Cuezva J. M., Mayor F. Non- gluconeogenic fate of lactate during the early neonatal period in the rat. FEBS Lett. 1980 May 19;114(1):132–134. doi: 10.1016/0014-5793(80)80876-3. [DOI] [PubMed] [Google Scholar]
  22. Okajima F., Ui M. Metabolism of glucose in hyper- and hypo-thyroid rats in vivo. Glucose-turnover values and futile-cycle activities obtained with 14C- and 3H-labelled glucose. Biochem J. 1979 Aug 15;182(2):565–575. doi: 10.1042/bj1820565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Pearce P. H., Buirchell B. J., Weaver P. K., Oliver I. T. The development of phosphopyruvate carboxylase and gluconeogenesis in neonatal rats. Biol Neonate. 1974;24(5):320–329. doi: 10.1159/000240664. [DOI] [PubMed] [Google Scholar]
  24. Pines M., Bashan N., Moses S. W. Glucose effect on glycogen synthetase and phosphorylase in fetal rat liver. FEBS Lett. 1976 Mar 1;62(3):301–303. doi: 10.1016/0014-5793(76)80080-4. [DOI] [PubMed] [Google Scholar]
  25. Pollak J. K. The interdependence of mitochondrial maturation and glycogen metabolism in perinatal rat liver. Biochem Soc Trans. 1977;5(1):341–348. doi: 10.1042/bst0050341. [DOI] [PubMed] [Google Scholar]
  26. Snell K., Walker D. G. Glucose metabolism in the newborn rat. Temporal studies in vivo. Biochem J. 1973 Apr;132(4):739–752. doi: 10.1042/bj1320739. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Spitzer J. J., Weng J. T. Removal and utilization of ketone bodies by the brain of newborn puppies. J Neurochem. 1972 Sep;19(9):2169–2173. doi: 10.1111/j.1471-4159.1972.tb05125.x. [DOI] [PubMed] [Google Scholar]
  28. Stalmans W., De Wulf H., Hue L., Hers H. G. The sequential inactivation of glycogen phosphorylase and activation of glycogen synthetase in liver after the administration of glucose to mice and rats. The mechanism of the hepatic threshold to glucose. Eur J Biochem. 1974 Jan 3;41(1):127–134. doi: 10.1111/j.1432-1033.1974.tb03252.x. [DOI] [PubMed] [Google Scholar]
  29. Vernon R. G., Walker D. G. Glucose metabolism in the developing rat. Studies in vivo. Biochem J. 1972 Apr;127(3):521–529. doi: 10.1042/bj1270521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. 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]
  31. Yeung D., Oliver I. T. Development of gluconeogenesis in neonatal rat liver. Effect of premature delivery. Biochem J. 1967 Dec;105(3):1229–1233. doi: 10.1042/bj1051229. [DOI] [PMC free article] [PubMed] [Google Scholar]

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