scholarly journals The role of glutamine oxidation and the purine nucleotide cycle for adaptation of tumour energetics to the transition from the anaerobic to the aerobic state

1988 ◽  
Vol 252 (2) ◽  
pp. 381-386 ◽  
Author(s):  
Z Kovacević ◽  
D Jerance ◽  
O Brkljac
Keyword(s):  
Adenine Nucleotide ◽  
The Other ◽  
Purine Nucleotide ◽  
Purine Nucleotide Cycle ◽  
Adenine Nucleotide Pool

It is proposed that the purine nucleotide cycle and glutamine oxidation play a key role in the adaptation of tumour energetics to the transition from the anaerobic to the aerobic state. In support of this proposal, it was found that glutamine and inosine markedly increase total adenylates in the presence of oxygen, whereas the addition of hadacidin abolishes this effect. Transition of the cells from the anaerobic to the aerobic state, and vice versa, in the presence of glutamine plus inosine revealed that there are two components of the adenine nucleotide pool, one which is stable and the other which is variable and responds to the aerobic-anaerobic transition. This part of the pool undergoes degradation or resynthesis owing to activation of the enzymes of the purine nucleotide cycle. Resynthesis of the pool is accompanied by substantial net utilization of aspartate, which is produced by glutamine oxidation. This is supported by the experiments in which the cells were alternately incubated with nitrogen or oxygen, demonstrating that hadacidin significantly decreased utilization of aspartate and regeneration of ATP owing to inhibition of adenylosuccinate synthase.

scholarly journals Mechanisms of adenosine 5'-monophosphate catabolism in human erythrocytes

Blood ◽  
1986 ◽  
Vol 67 (4) ◽  
pp. 988-992 ◽  
Author(s):  
DE Paglia ◽  
WN Valentine ◽  
M Nakatani ◽  
RA Brockway
Keyword(s):  
Potential Role ◽  
Adenine Nucleotide ◽  
Acidic Ph ◽  
Amp Deaminase ◽  
Severe Deficiency ◽  
Erythrocyte Enzyme ◽  
Senescent Erythrocytes ◽  
Adenine Nucleotide Pool ◽  
Normal Controls

Abstract Uncertainties regarding the role of pyrimidine nucleotidase (PyrNase) in AMP catabolism were resolved by studies of erythrocytes from normal controls, controls with young mean cell ages, and patients with hereditary hemolytic anemia due to severe deficiency of PyrNase. Hemolysates from the latter exhibited undiminished capacity to dephosphorylate AMP over a broad range of pH, indicating that PyrNase was not directly involved. In each subject group, the rates of AMP dephosphorylation between pH 5.1 and 8.3 were indistinguishable from those of IMP, suggesting a potential role for AMP-deaminase, an erythrocyte enzyme that was stimulated by coformycin at pH 7.2. Quantitative analysis of catabolites in incubated hemolysates confirmed that AMP degradation preferentially occurred via deamination to IMP with subsequent dephosphorylation by another erythrocyte nucleotidase isozyme, deoxyribonucleotidase. Both AMP-deaminase and deoxyribonucleotidase have acidic pH optima with minimal activities at physiologic pH, suggesting that this pathway of AMP catabolism could accelerate depletion of the adenine nucleotide pool and thereby mediate the demise of senescent erythrocytes sequestered in the spleen.

scholarly journals Sources of ammonia for mammalian urea synthesis

1978 ◽  
Vol 176 (3) ◽  
pp. 733-737 ◽  
Author(s):  
H A Krebs ◽  
R Hems ◽  
P Lund ◽  
D Halliday ◽  
W W Read
Keyword(s):  
Glutamate Dehydrogenase ◽  
Initial Rate ◽  
Adenine Nucleotides ◽  
Rat Hepatocytes ◽  
The Other ◽  
Amino Group ◽  
Urea Synthesis ◽  
Purine Nucleotide ◽  
Carbamoyl Phosphate ◽  
Purine Nucleotide Cycle

The initial rate of incorporation of [15N]alanine into the 6-amino group of the adenine nucleotides in rat hepatocytes was about one-eighteenth of the rate of incorporation into urea. Thus the purine nucleotide cycle cannot provide most of the ammonia needed in urea synthesis for the carbamoyl phosphate synthase reaction (EC 2.7.2.5). On the other hand, contrary to the view expressed by McGivan & Chappell [(1975) FEBS Lett. 52, 1–7], the experiments support the view that hepatic glutamate dehydrogenase can supply the required ammonia.

scholarly journals Mechanisms of adenosine 5'-monophosphate catabolism in human erythrocytes

Blood ◽  
1986 ◽  
Vol 67 (4) ◽  
pp. 988-992
Author(s):  
DE Paglia ◽  
WN Valentine ◽  
M Nakatani ◽  
RA Brockway
Keyword(s):  
Potential Role ◽  
Adenine Nucleotide ◽  
Acidic Ph ◽  
Amp Deaminase ◽  
Severe Deficiency ◽  
Erythrocyte Enzyme ◽  
Senescent Erythrocytes ◽  
Adenine Nucleotide Pool ◽  
Normal Controls

Uncertainties regarding the role of pyrimidine nucleotidase (PyrNase) in AMP catabolism were resolved by studies of erythrocytes from normal controls, controls with young mean cell ages, and patients with hereditary hemolytic anemia due to severe deficiency of PyrNase. Hemolysates from the latter exhibited undiminished capacity to dephosphorylate AMP over a broad range of pH, indicating that PyrNase was not directly involved. In each subject group, the rates of AMP dephosphorylation between pH 5.1 and 8.3 were indistinguishable from those of IMP, suggesting a potential role for AMP-deaminase, an erythrocyte enzyme that was stimulated by coformycin at pH 7.2. Quantitative analysis of catabolites in incubated hemolysates confirmed that AMP degradation preferentially occurred via deamination to IMP with subsequent dephosphorylation by another erythrocyte nucleotidase isozyme, deoxyribonucleotidase. Both AMP-deaminase and deoxyribonucleotidase have acidic pH optima with minimal activities at physiologic pH, suggesting that this pathway of AMP catabolism could accelerate depletion of the adenine nucleotide pool and thereby mediate the demise of senescent erythrocytes sequestered in the spleen.

scholarly journals Changes of nucleotide content in human and rat heart during cardiac surgery and ischemia.

1993 ◽  
Vol 40 (4) ◽  
pp. 531-538 ◽  
Author(s):  
R T Smoleński ◽  
A C Składanowski ◽  
J Swierczyński ◽  
M Perko ◽  
M Narkiewicz ◽  
...  
Keyword(s):  
Cardiac Surgery ◽  
Rat Heart ◽  
Human Heart ◽  
Adenine Nucleotide ◽  
Heart Defects ◽  
Human Myocardium ◽  
Purine Nucleotide ◽  
Initial Value ◽  
Adenylate Pool ◽  
Adenine Nucleotide Pool

The influence of ischemia on purine nucleotide and their catabolite concentration in human myocardium was investigated during surgery of acquired and congenital heart defects. This was compared with the influence of ischemia on rat heart. Concentrations of adenine and guanine nucleotides and their catabolites were measured in the extracts of heart biopsies taken at the onset of ischemia and at the time of reperfusion. The content of myocardial ATP in human heart decreased from the initial value of 22.3 +/- 1.1 to 14.6 +/- 1.5 nmol/mg protein and total adenine nucleotide pool decreased from 34.2 +/- 1.8 to 27.6 +/- 1.5 nmol/mg protein during the operation. Significant increases in myocardial concentrations of purine catabolites were also observed with the most prominent rise in inosine from below 0.5 at the onset of the ischemia to 3.0 +/- 0.5 nmol/mg protein at the time of reperfusion. A positive correlation was demonstrated between the concentration of purine catabolites in the heart at the end of ischemia with the decrease of both ATP and the total nucleotide pool. An interesting metabolic specificity of the ischemic human heart appeared to be only a small accumulation of inosine monophosphate (IMP). The increase of IMP in the rat heart after ischemia was several-fold higher. Thus, cardiac surgery of congenital and acquired heart defects was associated with a significant decrease in myocardial adenylate pool and a single biopsy collected at the end of ischemia seems to be sufficient to evaluate the extent of this metabolic and possibly functional impairment of the heart.

scholarly journals Systematic variations in the content of the purine nucleotides in the steady-state perfused rat heart. Evidence for the existence of controlled storage and release of adenine nucleotides

1978 ◽  
Vol 176 (2) ◽  
pp. 485-493 ◽  
Author(s):  
David J. Bates ◽  
David Perrett ◽  
John Mowbray
Keyword(s):  
Cyclic Amp ◽  
Rat Heart ◽  
Energy Demand ◽  
De Novo ◽  
Adenine Nucleotide ◽  
Adenine Nucleotides ◽  
Purine Nucleotide ◽  
Purine Nucleotides ◽  
Perfused Rat Heart ◽  
Adenine Nucleotide Pool

1. The contents of the major purine nucleotides in the isolated non-working perfused rat heart varied systematically during 80min of perfusion. In particular the amounts of ATP, ADP, GTP, cyclic AMP and cyclic GMP in the well-oxygenated myocardium showed changes ranging from 25 to 60% of the mean concentrations. The apparent periodicity was about 30min for some and about 60min for other nucleotides. 2. These data are in contrast with measurements of parameters reflecting heart performance, which remained constant over this period of perfusion. 3. The ATP/ADP ratio, the cyclic AMP content, the GTP content and the GTP/GDP ratio in the tissue bore a constant relationship to one another, and all showed the same temporal variation. 4. Increasing the energy demand on the heart by administration of bovine somatotropin (1μg/ml) tended to damp the variations, and generally lower the content of all the nucleotides. 5. The total extractable adenine nucleotide pool also showed systematic temporal variations of as much as 1.3μmol/g wet wt. of tissue within 10min. 6. These variations could not be accounted for as inter-conversion with adenosine, other purine nucleotides, nucleosides or purine-degradation products either in the tissue or in the perfusion medium. No evidence was found in this preparation of the purine nucleotide oscillations described by Lowenstein and his co-workers [see Tornheim & Lowenstein (1975) J. Biol. Chem.250, 6304–6314]. 7. Further, the pool size increases cannot be satisfactorily explained by either synthesis de novo or the breakdown of any purine macromolecular species in the cell. Thus it is suggested that an unsuspected substantial storage form of purine nucleotide may exist in heart.

scholarly journals Mechanism and control of degradation and resynthesis of adenylates in tumour cells

1991 ◽  
Vol 273 (2) ◽  
pp. 277-281 ◽  
Author(s):  
Z Kovačević ◽  
O Brkljač ◽  
D Jeranče
Keyword(s):  
Adenine Nucleotide ◽  
Essential Feature ◽  
Ehrlich Ascites Carcinoma ◽  
Hepatoma Cells ◽  
Tumour Cells ◽  
Ehrlich Ascites ◽  
Purine Nucleotide Cycle ◽  
Adenine Nucleotide Pool ◽  
Energy Buffer ◽  
And Control

A comparative study revealed that Ehrlich ascites carcinoma (EAC) cells use glutamine plus inosine for regeneration of adenylates via the purine nucleotide cycle, whereas AS 30D hepatoma cells use adenosine instead. This observation can be correlated with the very low production of aspartate from glutamine in hepatoma cells. Although glucose is an important energy fuel for EAC, it cannot maintain a high enough level of adenylates unless glutamine is also present. Kinetic analysis of hydrolysis of ATP and ADP in the presence of rotenone suggests that deamination of AMP does not maintain a high enough ATP/ADP ratio and probably does not act as energy buffer after inhibition of cell respiration. It seems that, compared with normal cells, malignant cells have the ability for a very rapid regeneration of adenylates. It is proposed that instability of the adenine nucleotide pool, owing to frequent aerobic-anaerobic transitions, represents an essential feature of neoplasia, with profound impact on the whole metabolism of tumour cells.

Plasma Levels of Protein S, Protein C, and Factor X: Effects of Sex, Hormonal State and Age

1995 ◽  
Vol 74 (05) ◽  
pp. 1271-1275 ◽  
Author(s):  
C M A Henkens ◽  
V J J Bom ◽  
W van der Schaaf ◽  
P M Pelsma ◽  
C Th Smit Sibinga ◽  
...  
Keyword(s):  
Regression Analysis ◽  
Postmenopausal Women ◽  
Protein C ◽  
Blood Donors ◽  
Premenopausal Women ◽  
Protein S ◽  
The Other ◽  
Factor X ◽  
Normal Ranges

SummaryWe measured total and free protein S (PS), protein C (PC) and factor X (FX) in 393 healthy blood donors to assess differences in relation to sex, hormonal state and age. All measured proteins were lower in women as compared to men, as were levels in premenopausal women as compared to postmenopausal women. Multiple regression analysis showed that both age and subgroup (men, pre- and postmenopausal women) were of significance for the levels of total and free PS and PC, the subgroup effect being caused by the differences between the premenopausal women and the other groups. This indicates a role of sex-hormones, most likely estrogens, in the regulation of levels of pro- and anticoagulant factors under physiologic conditions. These differences should be taken into account in daily clinical practice and may necessitate different normal ranges for men, pre- and postmenopausal women.

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