On the reliability of 13C metabolic modeling with two-compartment neuronal-glial models

被引:33
作者
Shestov, Alexander A. [1 ]
Valette, Julien [1 ]
Ugurbil, Kamil [1 ]
Henry, Pierre-Gilles [1 ]
机构
[1] Univ Minnesota, Ctr Magnet Resonance Res, Minneapolis, MN 55455 USA
关键词
metabolic modeling; C-13; magnetic resonance spectroscopy; neuronal-glial compartmentation; glutamate-glutamine cycle;
D O I
10.1002/jnr.21269
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Metabolic modeling of C-13 NMR spectroscopy (C-13 MRS) data using two-compartment neuronal-glial models enabled non-invasive measurements of the glutamate-glutamine cycle rate (V-NT) in the brain in vivo. However, the reliability of such two-compartment metabolic modeling has not been examined thoroughly. This study uses Monte-Carlo simulations to investigate the reliability of metabolic modeling of C-13 positional enrichment time courses measured in brain amino acids such as glutamate and glutamine during [1- C-13]- or [1,6- C-13(2)]glucose infusion. Results show that the determination Of VNT is not very precise under experimental conditions typical of in vivo NMR studies, whereas the neuronal TCA cycle rate V-TCA(N) is determined with a much higher precision. Consistent with these results, simulated C-13 positional enrichment curves for glutamate and glutamine are much more sensitive to the value Of V-TCA(N) than to the value of V-NT. We conclude that the determination of the glutamate-glutamine cycle rate V-NT using C-13 MRS is relatively unreliable when fitting C-13 positional enrichment curves obtained during [1- C-13] or [1,6- C-13(2)]glucose infusion. Further developments are needed to improve the determination Of V-NT, for example using additional information from C-13-C-13 isotoporners and/or using glial specific substrates such as [2- C-13]acetate. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:3294 / 3303
页数:10
相关论文
共 38 条
[31]   In vivo NMR studies of the glutamate neurotransmitter flux and neuroenergetics: Implications for brain function [J].
Rothman, DL ;
Behar, KL ;
Hyder, F ;
Shulman, RG .
ANNUAL REVIEW OF PHYSIOLOGY, 2003, 65 :401-427
[32]   Determination of the rate of the glutamate glutamine cycle in the human brain by in vivo 13C NMR [J].
Shen, J ;
Petersen, KF ;
Behar, KL ;
Brown, P ;
Nixon, TW ;
Mason, GF ;
Petroff, OAC ;
Shulman, GI ;
Shulman, RG ;
Rothman, DL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (14) :8235-8240
[33]   13C magnetic resonance spectroscopy studies of alterations in glutamate neurotransmission [J].
Shen, J .
BIOLOGICAL PSYCHIATRY, 2006, 59 (10) :883-887
[34]   Stoichiometric coupling of brain glucose metabolism and glutamatergic neuronal activity [J].
Sibson, NR ;
Dhankhar, A ;
Mason, GF ;
Rothman, DL ;
Behar, KL ;
Shulman, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :316-321
[35]   In vivo C-13 NMR measurements of cerebral glutamine synthesis as evidence for glutamate-glutamine cycling [J].
Sibson, NR ;
Dhankhar, A ;
Mason, GF ;
Behar, KL ;
Rothman, DL ;
Shulman, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2699-2704
[36]   In vivo 13C NMR measurement of neurotransmitter glutamate cycling, anaplerosis and TCA cycle flux in rat brain during [2-13C]glucose infusion [J].
Sibson, NR ;
Mason, GF ;
Shen, J ;
Cline, GW ;
Herskovits, AZ ;
Wall, JEM ;
Behar, KL ;
Rothman, DL ;
Shulman, RG .
JOURNAL OF NEUROCHEMISTRY, 2001, 76 (04) :975-989
[37]   Preferential utilization of acetate by astrocytes is attributable to transport [J].
Waniewski, RA ;
Martin, DL .
JOURNAL OF NEUROSCIENCE, 1998, 18 (14) :5225-5233
[38]   In vivo evidence for reduced cortical glutamate-glutamine cycling in rats treated with the antidepressant/antipanic drug phenelzine [J].
Yang, J ;
Shen, J .
NEUROSCIENCE, 2005, 135 (03) :927-937