Literature DB >> 5144216

The metabolism of glucose 6-phosphate by mammalian cerebral cortex in vitro.

P R Dodd, H F Bradford, E B Chain.   

Abstract

1. The metabolism of glucose 6-phosphate in rat cerebral-cortex slices in vitro was compared with that of glucose. It was found that a glucose 6-phosphate concentration of 25mm was required to achieve maximal oxygen uptake rates and ATP concentrations, whereas only 2mm-glucose was required. 2. When 25mm-[U-(14)C]glucose 6-phosphate was used as substrate, the pattern of labelling of metabolites was found to be quantitatively and qualitatively similar to the pattern found with 10mm-[U-(14)C]glucose, except that incorporation into [(14)C]lactate was decreased, and significant amounts of [(14)C]glucose and [(14)C]mannose phosphate and [(14)C]fructose phosphate were formed. 3. Unlabelled glucose (10mm) caused a tenfold decrease in the incorporation of 25mm-[U-(14)C]glucose 6-phosphate into all metabolites except [(14)C]glucose and [(14)C]mannose phosphate and [(14)C]fructose phosphate. In contrast, unlabelled glucose 6-phosphate (25mm) had no effect on the metabolism of 10mm-[U-(14)C]glucose other than to increase markedly the incorporation into, and amount of, [(14)C]lactate, the specific radioactivity of this compound remaining approximately the same. 4. The effect of glucose 6-phosphate in increasing lactate formation from glucose was found to occur also with a number of other phosphate esters and with inorganic phosphate. Further investigation indicated that the effect was probably due to binding of medium calcium by the phosphate moiety, thereby de-inhibiting glucose uptake. 5. Incubations carried out in a high-phosphate high-potassium medium gave a pattern of metabolism similar to that found when slices were subjected to depolarizing conditions. Tris-buffered medium gave similar results to bicarbonate-buffered saline, except that it allowed much less lactate formation from glucose. 6. Part of the glucose formed from glucose 6-phosphate was extracellular and was produced at a rate of 12mumol/h per g of tissue in Krebs tris medium when glycolysis was blocked. The amount formed was much less when 25mm-P(i) or 26mm-HCO(3) (-) was present, the latter being in the absence of tris. 7. Glucose 6-phosphate also gave rise to an intracellular glucose pool, whereas no intracellular glucose was detectable when glucose was the substrate.

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Year:  1971        PMID: 5144216      PMCID: PMC1178265          DOI: 10.1042/bj1251027

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  15 in total

1.  CONTINUOUS RECORDINGS OF CHANGES IN MEMBRANE POTENTIAL IN MAMMALIAN CEREBRAL TISSUES IN VITRO; RECOVERY AFTER DEPOLARIZATION BY ADDED SUBSTANCES.

Authors:  I M GIBSON; H MCILWAIN
Journal:  J Physiol       Date:  1965-01       Impact factor: 5.182

2.  [Phosphomannose isomerase. I. Activity measurement and dependence of enzyme action on sulfhydryl groups and metals in some animal tissues].

Authors:  F H BRUNS; E NOLTMANN; A WILLEMSEN
Journal:  Biochem Z       Date:  1958

3.  Pyridine nucleotide transhydrogenase. VII. Determination of the reactions with coenzyme analogues in mammalian tissues.

Authors:  A M STEIN; N O KAPLAN; M M CIOTTI
Journal:  J Biol Chem       Date:  1959-04       Impact factor: 5.157

4.  The intracellular distribution of glycolytic and other enzymes in rat-brain homogenates and mitochondrial preparations.

Authors:  M K JOHNSON
Journal:  Biochem J       Date:  1960-12       Impact factor: 3.857

5.  The non-competitive inhibition of brain hexokinase by glucose-6-phosphate and related compounds.

Authors:  R K CRANE; A SOLS
Journal:  J Biol Chem       Date:  1954-10       Impact factor: 5.157

6.  The phosphorylase reaction. II. The influence of magnesium ions on equilibrium.

Authors:  W E TREVELYAN; P F E MANN; J S HARRISON
Journal:  Arch Biochem Biophys       Date:  1952-08       Impact factor: 4.013

7.  Inhibitory effect of physiological bicarbonate ion levels on the activities of glucose 6-phosphate phosphohydrolase.

Authors:  J E Dyson; W B Anderson; R C Nordlie
Journal:  J Biol Chem       Date:  1969-02-25       Impact factor: 5.157

8.  Metabolism of glucose and glutamate by synaptosomes from mammalian cerebral cortex.

Authors:  H F Bradford; A J Thomas
Journal:  J Neurochem       Date:  1969-11       Impact factor: 5.372

9.  Metabolism of glucose-6-phosphate in slices of rat brain cortex.

Authors:  M Balliano; I Masi; F Pocchiari
Journal:  Brain Res       Date:  1969-03       Impact factor: 3.252

10.  Conversion of glucose phosphate-14C to glucose-14C in passage through human brain in vivo.

Authors:  W Sacks; S Sacks
Journal:  J Appl Physiol       Date:  1968-06       Impact factor: 3.531

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  4 in total

1.  Regional distribution of glucose in mouse brain.

Authors:  M Shimada; T Kihara; M Watanabe; K Kurimoto
Journal:  Neurochem Res       Date:  1977-12       Impact factor: 3.996

2.  Formation of glucose from glucose 6-phosphate by rat brain slices.

Authors:  P R Dodd; H F Bradford; E B Chain
Journal:  Biochem J       Date:  1972-04       Impact factor: 3.857

3.  Fractionation of nuclei from brain by zonal centrifugation and a study of the ribonucleic acid polymerase activity in the various classes of nuclei.

Authors:  J Austoker; D Cox; A P Mathias
Journal:  Biochem J       Date:  1972-10       Impact factor: 3.857

4.  A comparison of the cerebral uptake and metabolism of labeled glucose and deoxyglucose in vivo in rats.

Authors:  W Sacks; S Sacks; A Fleischer
Journal:  Neurochem Res       Date:  1983-05       Impact factor: 3.996

  4 in total

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