Uptake of Glucose Analogues into Cultured Cerebral Microvessel Endothelium

1985 ◽  
Vol 44 (5) ◽  
pp. 445-458 ◽  
Author(s):  
HARRY V. VINTERS ◽  
DAVID W. BECK ◽  
JAMES V. BREADY ◽  
KAREN MAXWELL ◽  
JUDITH A. BERLINER ◽  
...  
1983 ◽  
Vol 42 (3) ◽  
pp. 339
Author(s):  
H. V. Vinters ◽  
P. A. Cancilia ◽  
J. Bready ◽  
D. w. Beck ◽  
M. N. Hart ◽  
...  

2019 ◽  
Author(s):  
Ashley Williams ◽  
Deborah Muoio ◽  
Guofang Zhang

Quantative measurements of the glucose analogue, 2-deoxyglucose (2DG), and its phosphorylated metabolite (2-deoxyglucose-6-phosphate (2DG-6-P)) are critical for the measurement of glucose uptake. While the field has long identified the need for sensitive and reliable assays that deploy non-radiolabled glucose analogues to assess glucose uptake, no analytical MS-based methods exist to detect trace amounts in complex biological samples. In the present work, we show that 2DG is poorly suited for MS-based methods due to interfering metabolites. We therefore developed and validated an alternative C18-based LC-Q-Exactive-Orbitrap-MS method using 2-fluoro-2-deoxyglucose (2FDG) to quantify both 2FDG and 2FDG-6-P by measuring the sodium adduct of 2FDG in the positive mode and deprotonation of 2FDG-6-P in the negative mode. The low detection limit of this method can reach 81.4 and 48.8 fmol for both 2FDG and 2FDG-6-P, respectively. The newly developed method was fully validated via calibration curves in the presence and absence of biological matrix. The present work is the first successful LC-MS method that can quantify trace amounts of a nonradiolabeled glucose analogue and its phosphorylated metabolite and is a promising analytical method to determine glucose uptake in biological samples.


1998 ◽  
Vol 48 (2) ◽  
pp. 241-248 ◽  
Author(s):  
Norman K. Matheson ◽  
David K. Myers
Keyword(s):  

1987 ◽  
Vol 8 (5-6) ◽  
pp. 299-310 ◽  
Author(s):  
G. Gil-Fernández ◽  
S. Pérez ◽  
P. Vilas ◽  
C. Pérez ◽  
F.G. de las Heras ◽  
...  

1984 ◽  
Vol 43 (3) ◽  
pp. 350
Author(s):  
H. V. Vinters ◽  
J. A. Berliner ◽  
K. Maxwell ◽  
J. V. Bready ◽  
P. A. Cancilla

1990 ◽  
Vol 259 (4) ◽  
pp. C660-C667 ◽  
Author(s):  
J. G. Reyes ◽  
M. V. Velarde ◽  
R. Ugarte ◽  
D. J. Benos

The impact of glycolysis on rat spermatid energy metabolism is made apparent by the simultaneous occurrence of the following three events upon glucose addition to the extracellular medium of a rat spermatid cell suspension: decrease in ATP content, exit of acid equivalents, and increased lactate production and efflux. In this work, we have studied the interrelations between these three phenomena. By measuring ATP content, net acid transport, lactate exit, oxygen consumption, intracellular pH, CO2 production, and glycolytic intermediates in the presence of glucose and glucose analogues, we conclude that 1) lactate production, decrease in ATP content, and acid equivalent exit are dependent on the metabolism of glucose up to different stages in glycolysis. 2) The decrease in ATP content is not directly related to the exit of acid equivalents from rat spermatids. 3) Glucose metabolism is a net ATP-consuming process at high intracellular ATP content but is a net ATP-producing process at low intracellular ATP concentration in rat spermatids. 4) Acid equivalent production arises from the metabolism of glucose beyond glyceraldehyde 3-phosphate dehydrogenase. 5) Lactic acid diffusion and/or lactate transport and CO2 production and exit could account for the glucose-dependent acid equivalent efflux in rat spermatids.


2020 ◽  
Vol 26 (59) ◽  
pp. 13499-13506 ◽  
Author(s):  
Jacob St‐Gelais ◽  
Émilie Côté ◽  
Danny Lainé ◽  
Paul A. Johnson ◽  
Denis Giguère

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