Measurement of cerebral oxidative glucose consumption in patients with type 1 diabetes mellitus and hypoglycemia unawareness using 13C nuclear magnetic …

PG Henry, AB Criego, A Kumar, ER Seaquist - Metabolism, 2010 - Elsevier
PG Henry, AB Criego, A Kumar, ER Seaquist
Metabolism, 2010Elsevier
The aim of the present study was to use 13C nuclear magnetic resonance (NMR) to
measure the cerebral oxidative metabolic rate of glucose (CMRglc [ox]) in patients with
diabetes and to compare these measurements with those collected from matched controls.
We elected to study a group with type 1 diabetes mellitus and hypoglycemia unawareness
because we had previously found such patients to have higher brain glucose concentrations
than healthy volunteers under steady-state conditions. We sought to determine if this …
The aim of the present study was to use 13C nuclear magnetic resonance (NMR) to measure the cerebral oxidative metabolic rate of glucose (CMRglc[ox]) in patients with diabetes and to compare these measurements with those collected from matched controls. We elected to study a group with type 1 diabetes mellitus and hypoglycemia unawareness because we had previously found such patients to have higher brain glucose concentrations than healthy volunteers under steady-state conditions. We sought to determine if this difference in steady-state brain concentrations could be explained by a difference in CMRglc(ox). Time courses of 13C label incorporation in brain amino acids were measured in occipital cortex during infusion of [1-13C]glucose. These time courses were fitted using a 1-compartment metabolic model to determine CMRglc(ox). Our results show that the tricarboxylic acid cycle (TCA) cycle rate (VTCA, which is twice CMRglc[ox]) in subjects with type 1 diabetes mellitus was not significantly different from that of healthy controls (0.84 ± 0.03 vs 0.79 ± 0.03 μmol/[g min], n = 5 in each group, mean ± SEM). We conclude that the changes in steady-state brain glucose concentrations that we observed in patients with type 1 diabetes mellitus in a previous study (J Neurosci Res. 2005;79:42-47) cannot be explained by changes in oxidative glucose consumption
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