Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1988 Jul 1;253(1):27–32. doi: 10.1042/bj2530027

Gluconeogenesis from glycine and serine in fasted normal and diabetic rats.

G Hetenyi Jr 1, P J Anderson 1, M Raman 1, C Ferrarotto 1
PMCID: PMC1149253  PMID: 3138983

Abstract

1. Non-anaesthetized normal and diabetic rats were fasted for 1 day, and [U-14C]glycine, or [U-14C]serine, or [U-14C]- plus [3-3H]-glucose was injected intra-arterially. The rates of synthesis de novo/irreversible disposal for glycine, serine and glucose, as well as the contribution of carbon atoms by the amino acids to plasma glucose, were calculated from the integrals of the specific-radioactivity-versus-time curves in plasma. 2. The concentrations of both glycine and serine in blood plasma were lower in diabetic than in fasted normal animals. 3. The rates of synthesis de novo/irreversible disposal of both amino acids tended to be lower in diabetic animals, but the decrease was statistically significant only for serine (14.3 compared with 10.5 mumol/min per kg). 4. Of the carbon atoms of plasma glucose, 2.9% arose from glycine in both fasted normal and diabetic rats, whereas 4.46% of glucose carbon originated from serine in fasted normal and 6.77% in diabetic rats. 5. As judged by their specific radioactivities, plasma serine and glycine exchange carbon atoms rapidly and extensively. 6. It was concluded that the turnover of glycine remains essentially unchanged, whereas that of serine is decreased in diabetic as compared with fasted normal rats. The plasma concentration of both amino acids was lower in diabetic rats. Both glycine and serine are glucogenic. In diabetic rats the contribution of carbon atoms from glycine to glucose increases in direct proportion to the increased glucose turnover, whereas the contribution by serine becomes also proportionally higher.

Full text

PDF
27

Selected References

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

  1. Beliveau G. P., Freedland R. A. Metabolism of serine, glycine and threonine in isolated cat hepatocytes Felis domestica. Comp Biochem Physiol B. 1982;71(1):13–18. doi: 10.1016/0305-0491(82)90168-7. [DOI] [PubMed] [Google Scholar]
  2. Bhatia S. C., Bhatia S., Rous S. Gluconeogenesis from L-serine in rat liver. Life Sci. 1975 Jul 15;17(2):267–273. doi: 10.1016/0024-3205(75)90514-7. [DOI] [PubMed] [Google Scholar]
  3. Bidlingmeyer B. A., Cohen S. A., Tarvin T. L. Rapid analysis of amino acids using pre-column derivatization. J Chromatogr. 1984 Dec 7;336(1):93–104. doi: 10.1016/s0378-4347(00)85133-6. [DOI] [PubMed] [Google Scholar]
  4. Chiasson J. L., Cook J., Liljenquist J. E., Lacy W. W. Glucagon stimulation of gluconeogenesis from alanine in the intact dog. Am J Physiol. 1974 Jul;227(1):19–23. doi: 10.1152/ajplegacy.1974.227.1.19. [DOI] [PubMed] [Google Scholar]
  5. Corney P. L., Heath D. F. A simple way of estimating turnover rates from specific activity--time curves. J Appl Physiol. 1970 May;28(5):672–674. doi: 10.1152/jappl.1970.28.5.672. [DOI] [PubMed] [Google Scholar]
  6. Golden S., Chenoweth M., Dunn A., Okajima F., Katz J. Metabolism of tritium- and 14C-labeled alanine in rats. Am J Physiol. 1981 Aug;241(2):E121–E128. doi: 10.1152/ajpendo.1981.241.2.E121. [DOI] [PubMed] [Google Scholar]
  7. Hayashi S., Tanaka T., Naito J., Suda M. Dietary and hormonal regulation of serine synthesis in the rat. J Biochem. 1975 Jan 1;77(1?):207–219. [PubMed] [Google Scholar]
  8. Hetenyi G., Jr Correction factor for the estimation of plasma glucose synthesis from the transfer of 14C-atoms from labelled substrate in vivo: A preliminary report. Can J Physiol Pharmacol. 1979 Jul;57(7):767–770. doi: 10.1139/y79-119. [DOI] [PubMed] [Google Scholar]
  9. Klim R. A., Albajar M., Hems R., Williamson D. H. Effects of chronic uraemia on the formation of glucose and urea plus ammonia from L-alanine, L-glutamine and L-serine in isolated rat hepatocytes. Clin Sci (Lond) 1986 Jun;70(6):627–634. doi: 10.1042/cs0700627. [DOI] [PubMed] [Google Scholar]
  10. Lowry M., Hall D. E., Hall M. S., Brosnan J. T. Renal metabolism of amino acids in vivo: studies on serine and glycine fluxes. Am J Physiol. 1987 Feb;252(2 Pt 2):F304–F309. doi: 10.1152/ajprenal.1987.252.2.F304. [DOI] [PubMed] [Google Scholar]
  11. Mak W. W., Pitot H. C. Increase of L-serine dehydratase activity under gluconeogenic conditions in adult-rat hepatocytes cultured on collagen gel/nylon mesh. Biochem J. 1981 Sep 15;198(3):499–504. doi: 10.1042/bj1980499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Nissim I., Lapidot A. Dynamic aspects of amino acid metabolism in alloxan-induced diabetes and insulin-treated rabbits: in vivo studies with 15N and gas chromatography-mass spectrometry. Biochem Med Metab Biol. 1986 Feb;35(1):88–100. doi: 10.1016/0885-4505(86)90063-0. [DOI] [PubMed] [Google Scholar]
  13. Remesy C., Fafournoux P., Demigne C. Control of hepatic utilization of serine, glycine and threonine in fed and starved rats. J Nutr. 1983 Jan;113(1):28–39. doi: 10.1093/jn/113.1.28. [DOI] [PubMed] [Google Scholar]
  14. Robert J. J., Bier D. M., Zhao X. H., Matthews D. E., Young V. R. Glucose and insulin effects on the novo amino acid synthesis in young men: studies with stable isotope labeled alanine, glycine, leucine, and lysine. Metabolism. 1982 Dec;31(12):1210–1218. doi: 10.1016/0026-0495(82)90006-3. [DOI] [PubMed] [Google Scholar]
  15. Rowsell E. V., Carnie J. A., Wahbi S. D., Al-Tai A. H., Rowsell K. V. L-serine dehydratase and L-serine-pyruvate aminotransferase activities in different animal species. Comp Biochem Physiol B. 1979;63(4):543–555. doi: 10.1016/0305-0491(79)90061-0. [DOI] [PubMed] [Google Scholar]
  16. Rowsell E. V., al-Tai A. H., Carnie J. A. Increased liver L-serine-pyruvate aminotransferase activity under gluconeogenic conditions. Biochem J. 1973 May;134(1):349–351. doi: 10.1042/bj1340349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sallach H. J., Sanborn T. A., Bruin W. J. Dietary and hormonal regulation of hepatic biosynthetic and catabolic enzymes of serine metabolism in rats. Endocrinology. 1972 Oct;91(4):1054–1063. doi: 10.1210/endo-91-4-1054. [DOI] [PubMed] [Google Scholar]
  18. Sandoval I. V., Sols A. Gluconeogenesis from serine by the serine-dehydratase-dependent pathway in rat liver. Eur J Biochem. 1974 Apr 16;43(3):609–616. doi: 10.1111/j.1432-1033.1974.tb03448.x. [DOI] [PubMed] [Google Scholar]
  19. Snell K. Enzymes of serine metabolism in normal, developing and neoplastic rat tissues. Adv Enzyme Regul. 1984;22:325–400. doi: 10.1016/0065-2571(84)90021-9. [DOI] [PubMed] [Google Scholar]

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

RESOURCES