## Abstract The hypothesis that the arterial input function (AIF) of gadolinium‐diethylenetriaminepentaacetic acid injected by intravenous bolus and measured by the change in the __T__~1~‐relaxation rate (Δ__R__~1~; __R__~1~ = 1/__T__~1~) of superior sagittal sinus blood (AIF‐I) approximates the AI
Oxidation of 14C-labeled compounds perfused by microdialysis in the brains of free-moving rats
✍ Scribed by H. Ronald Zielke; Carol L. Zielke; Peter J. Baab
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 154 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
The oxidative capacity of the brain for alternate substrates, glucose, lactate, pyruvate, acetate, glutamate, and glutamine was determined by using microdialysis to infuse ^14^C‐labeled compounds into the interstitial fluid of adult rat brain and by collecting the brain‐generated ^14^CO~2~ from the dialysis eluate. All compounds were readily oxidized. The recovery of ^14^CO~2~ was enhanced for those compounds metabolically close to entry into the TCA cycle or known to have a low interstitial concentration. Two compounds, pyruvate and lactate, demonstrated reciprocal competition when added as nonradioactive competitors. Oxidation of two amino acids, ^14^C‐glutamate and ^14^C‐glutamine, was stimulated by the addition of nonradioactive acetate and pyruvate. α‐Cyano‐4‐hydroxycinnamate decreased ^14^C‐lactate and ^14^C‐pyruvate oxidation, consistent with the transport of both compounds via a monocarboxylate transporter. The results of this in vivo study support the results of previous in vitro studies that showed that a wide range of compounds formed from glucose in the brain are also oxidized in the brain for energy production. © 2007 Wiley‐Liss, Inc.
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