Horm Metab Res 2004; 36(5): 281-285
DOI: 10.1055/s-2004-814481
Original Basic
© Georg Thieme Verlag Stuttgart · New York

Metabolism of D-Glucose Anomers in Rat Pancreatic Islets Exposed to Equilibrated D-Glucose

W.  J.  Malaisse1 , Y.  Zhang1 , H.  Jijakli1 , P.  Courtois1 , A.  Sener1
  • 1Laboratory of Experimental Hormonology, Brussels Free University, Brussels, Belgium
Further Information

Publication History

Received 12 August 2003

Accepted after Revision 4 November 2003

Publication Date:
24 May 2004 (online)

Abstract

This study aims at establishing the contribution of α- and β-D-glucose to the total generation of 3HOH by rat pancreatic islets exposed to D-[2 - 3H]glucose or D-[5 - 3H] glucose at anomeric equilibrium. The islets were incubated for 60 min at 4 °C in the presence of equilibrated D-glucose (2.8 and 8.3 mM) mixed with tracer amounts of either α- or β-D-glucose labelled with tritium on either the C2 or C5 of the hexose. Relative to their respective concentrations, 3HOH generation from the anomers labelled with tritium on the C2 or C5 of the hexose provided β/α ratios comparable to those previously found at both 2.8 and 8.3mM, when the islets were exposed to each anomer separately. The relative contributions of each anomer to the total generation of 3HOH was also close to the theoretical values derived from mathematical models for the catabolism of D-glucose at anomeric equilibrium in rat islets at both 2.8 and 8.3 mM and in the case of both D-[2 - 3H]glucose and D-[5 - 3H]glucose. Thus, even in islets exposed to D-glucose at anomeric equilibrium, the metabolic fate of α-D-glucose differs vastly from that of β-D-glucose, the enzyme-to-enzyme channelling between hexokinase isoenzymes, especially glucokinase, and phosphoglucoisomerase being restricted to α-D-glucose 6-phosphate.

References

  • 1 Malaisse W J, Zhang Y, Jijakli H, Courtois P, Sener A. Enzyme-to-enzyme channelling of D-glucose 6-phosphate between glucokinase and phosphoglucoisomerase in rat pancreatic islets. Late-breaking abstracts of the 63rd Annual Meeting of the American Diabetes Association 2003; 12. 
  • 2 Malaisse W J, Zhang Y, Jijakli H, Courtois P, Sener A. Enzyme-to-enzyme channelling of early glycolytic metabolites in rat pancreatic islets.  Eur J Biochem. 2003;  270 (suppl 1) 59 (abstract)
  • 3 Zhang Y, Jijakli H, Courtois P, Sener A, Malaisse W J. Metabolism of tritiated D-glucose anomers in rat erythrocytes.  Mol Cell Biochem. 2004;  in press
  • 4 Malaisse W J, Deleers M, Malaisse-Lagae F, Sener A. Anomeric specificity of hexose metabolism in pancreatic islets. In: Mngola EN (ed) Diabetes 1982. Excerpta Medica ICS 1983 600: 345-351
  • 5 Miwa I, Okuda J, Niki H, Niki A. Uptake of radioactive D-glucose anomers by pancreatic islets.  J Biochem. 1975;  78 1109-1111
  • 6 Sener A, Leclercq-Meyer V, Marchand J, Giroix M-H, Dufrane S P, Malaisse W J. Is glucokinase responsible for the anomeric specificity of glycolysis in pancreatic islets?.  J Biol Chem. 1985;  260 12 978-12 981
  • 7 Malaisse-Lagae F, Malaisse W J. Insulin release by pancreatic islets. In: Larner J, Pohl SL (eds) Methods in Diabetes Research. New York; Wiley 1984: vol. I, part B, pp. 147-152
  • 8 Malaisse W J, Maggetto C, Leclercq-Meyer V, Sener A. Interference of glycogenolysis with glycolysis in pancreatic islets from glucose-infused rats.  J Clin Invest. 1993;  91 432-436
  • 9 Ashcroft S JH, Weerasinghe L CC, Bassett J M, Randle P J. The pentose cycle and insulin release in mouse pancreatic islets.  Biochem J. 1972;  126 525-532
  • 10 Malaisse W J, Sener A. Hexose metabolism in pancreatic islets. Feedback control of D-glucose oxidation by functional events.  Biochim Biophys Acta. 1988;  971 246-254
  • 11 Malaisse W J, Sener A, Carpinelli A R, Anjaneyulu K, Lebrun P, Herchuelz A, Christophe J. The stimulus-secretion coupling of glucose-induced insulin release. XLVI. Physiological role of L-glutamine as a fuel for pancreatic islets.  Mol Cell Endocrinol. 1980;  20 171-189
  • 12 Sener A, Malaisse-Lagae F, Dufrane S P, Malaisse W J. The coupling of metabolic to secretory events in pancreatic islets. The cytosolic redox state.  Biochem J. 1984;  220 433-440
  • 13 Willem R, Biesemans M, Hallenga K, Lippens G, Malaisse-Lagae F, Malaisse W J. Dual anomeric specificity and dual anomerase activity of phosphoglucoisomerase quantified by two-dimensional phase sensitive 13C EXSY NMR.  J Biol Chem. 1992;  267 210-217
  • 14 Malaisse W J, Bodur H. Hexose metabolism in pancreatic islets. Enzyme-to-enzyme tunnelling of hexose 6-phosphates.  Int J Biochem. 1991;  23 1471-1481
  • 15 Zähner D, Malaisse W J. Enzyme-to-enzyme tunneling between phosphoglucoisomerase and phosphofructokinase.  Int J Biochem. 1993;  25 1303-1307
  • 16 Randle P J, Hales C N. Insulin release mechanisms. In: Steiner DF, Freinkel N (eds) Handbook of Physiology (Section 7, Volume I). Washington; American Physiological Society 1972: 219-235
  • 17 Malaisse W J, Sener A, Koser M, Herchuelz A. The stimulus-secretion coupling of glucose-induced insulin release. XXIV. The metabolism of α- and β-D-glucose in isolated islets.  J Biol Chem. 1976;  251 5936-5943
  • 18 Malaisse W J. Physiology of insulin secretion and its alteration in diabetes: the concept of glucotoxicity. In: Andreani D, Gueriguian JL, Striker GE (eds) Diabetic complications: epidemiology and pathogenetic mechanisms. New York; Raven Press 1991: 3-23
  • 19 Malaisse W J. The anomeric malaise: a manifestation of B-cell glucotoxicity.  Horm Metab Res. 1991;  23 307-311

W. J. Malaisse

Laboratory of Experimental Hormonology · Brussels Free University

Route de Lennik 808 · 1070 Brussels · Belgium

Phone: +32(2)5556237

Fax: +32(2)5556356

Email: malaisse@ulb.ac.be