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Open AccessJournal ArticleDOI

Effect of glucagon on metabolite compartmentation in isolated rat liver cells during gluconeogenesis from lactate.

Elmar A. Siess, +3 more
- 15 Aug 1977 - 
- Vol. 166, Iss: 2, pp 225-235
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TLDR
The changes of the subcellular metabolite distribution after glucagon are compatible with the proposal that the stimulation of gluconeogenesis results from as yet unknown action(s) of the hormone at the mitochondrial level in concert with its established effects on proteolysis and lipolysis.
Abstract
1 The subcellular distribution of adenine nucleotides, acetyl-CoA, CoA, glutamate, 2-oxoglutarate, malate, oxaloacetate, pyruvate, phosphoenolpyruvate, 3-phosphoglycerate, glucose 6-phosphate, aspartate and citrate was studied in isolated hepatocytes in the absence and presence of glucagon by using a modified digitonin procedure for cell fractionation 2 In the absence of glucagon, the cytosol contains about two-thirds of cellular ATP, some 40–50% of ADP, acetyl-CoA, citrate and phosphoenolpyruvate, more than 75% of total 2-oxoglutarate, glutamate, malate, oxaloacetate, pyruvate, 3-phosphoglycerate and aspartate, and all of glucose 6-phosphate 3 In the presence of glucagon the cytosolic space shows an increase in the content of malate, phosphoenolpyruvate and 3-phosphoglycerate by more than 60%, and those of aspartate and glucose 6-phosphate rise by about 25% Other metabolites remain unchanged After glucagon treatment, cytosolic pyruvate is decreased by 37%, whereas glutamate and 2-oxoglutarate decrease by 70% The [NAD+]/[NADH] ratios calculated from the cytosolic concentrations of the reactants of lactate dehydrogenase and malate dehydrogenase were the same Glucagon shifts this ratio and also that of the [NADP+]/[NADPH] couple towards a more reduced state 4 In the mitochondrial space glucagon causes an increase in the acetyl-CoA and ATP contents by 25%, and an increase in [phosphoenolpyruvate] by 50% Other metabolites are not changed by glucagon Oxaloacetate in the matrix is only slightly decreased after glucagon, yet glutamate and 2-oxoglutarate fall to about 25% of the respective control values The [NAD+]/[NADH] ratios as calculated from the [3-hydroxybutyrate]/[acetoacetate] ratio and from the matrix [malate]/[oxaloacetate] couple are lowered by glucagon, yet in the latter case the values are about tenfold higher than in the former 5 Glucagon and oleate stimulate gluconeogenesis from lactate to nearly the same extent Oleate, however, does not produce the changes in cellular 2-oxoglutarate and glutamate as observed with glucagon 6 The changes of the subcellular metabolite distribution after glucagon are compatible with the proposal that the stimulation of gluconeogenesis results from as yet unknown action(s) of the hormone at the mitochondrial level in concert with its established effects on proteolysis and lipolysis

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The regulation of the matrix volume of mammalian mitochondria in vivo and in vitro and its role in the control of mitochondrial metabolism.

TL;DR: The methods by which the intra-mitochondrial volume is measured both in vitro and in situ are described, the mechanisms thought to regulate the mitochondrial volume are summarised and evidence that changes in mitochondrial volume may be important in the responses of a variety of tissues to hormones and other stimuli is provided.
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Generation of reactive oxygen species in the reaction catalyzed by α-ketoglutarate dehydrogenase

TL;DR: It is demonstrated that α-KGDH is able to generate H2O2 and, thus, could also be a source of reactive oxygen species (ROS) in mitochondria and significantly contribute to generation of oxidative stress in the mitochondria.
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Evidence for the participation of independent translocation for phosphate and glucose 6-phosphate in the microsomal glucose-6-phosphatase system. Interactions of the system with orthophosphate, inorganic pyrophosphate, and carbamyl phosphate.

TL;DR: Analysis of the kinetic data in combination with findings from other studies that a variety of inhibitors of the glucose-6-P translocase (T1) does not affect PPi hydrolysis provide compelling evidence that permeability of microsomes to Pi, PPi, and carbamyl-P is mediated by a second translocases (T2).
References
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Journal ArticleDOI

Removal of Fatty Acids from Serum Albumin by Charcoal Treatment

TL;DR: Fluorescence spectra of human serum albumin samples indicated that impurities are sometimes present which can be removed by charcoal at neutral pH, and acid-charcoal treatment is a much more rapid method of removing lipid impurities than other methods previously described.
Journal ArticleDOI

The redox state of free nicotinamide–adenine dinucleotide phosphate in the cytoplasm of rat liver

TL;DR: The application of the method of calculation to data published by Kraupp, Adler-Kastner, Niessner & Plank (1967), Goldberg, Passonneau & Lowry (1966) and Kauffman, Brown,passonneau and Lowry (1968) shows that the redox states of the NAD and NADP couples in cardiac-muscle cytoplasm and in mouse-brain cytop lasm are of the same order as those in rat liver.
Journal ArticleDOI

Mechanism for the stimulation of gluconeogenesis by fatty acids in perfused rat liver.

TL;DR: Results reported here indicate that in short-term experiments, the rate of gluconeogenesis can be controlled at the glyceraldehyde-3-P dehydrogenase step by the cellular level of DPNH.
Journal ArticleDOI

The rate of gluconeogenesis from various precursors in the perfused rat liver.

TL;DR: Two sites of action of glucagon must therefore be postulated: one concerned with mobilization of liver glycogen, the other with the promotion of gluconeogenesis.
Journal ArticleDOI

Control Mechanisms of Gluconeogenesis and Ketogenesis I. EFFECTS OF OLEATE ON GLUCONEOGENESIS IN PERFUSED RAT LIVER

TL;DR: Oleate increased the state of reduction of the pyridine nucleotide systems in both mitochondrial and cytosolic spaces as shown by increases in the ratios of lactate to pyruvate, β-hydroxybutyrate to acetoacetate, and malate to oxalacetate.
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