In vivo 13C NMR studies of compartmentalized cerebral carbohydrate metabolism

被引:91
作者
Gruetter, R [1 ]
机构
[1] Univ Minnesota, Dept Radiol & Neurosci, Ctr MR Res, Minneapolis, MN 55455 USA
关键词
NMR studies; cerebral carbohydrate metabolism; glycogen; glutamine;
D O I
10.1016/S0197-0186(02)00034-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Localized C-13 nuclear magnetic resonance (NMR) spectroscopy provides a unique window for studying cerebral carbohydrate metabolism through, e.g. the completely non-invasive measurement of cerebral glucose and glycogen metabolism. In addition, label incorporation into amino acid neurotransmitters such as glutamate (Glu), GABA and aspartate can be measured providing information on Krebs cycle flux and oxidative metabolism. Given the compartmentation of key enzymes such as pyruvate carboxylase and glutamine synthetase, the detection of label incorporation into glutamine indicated that neuronal and glial metabolism can be measured in vivo. The purpose of this paper is to provide a critical overview of these recent advances into measuring compartmentation of brain energy metabolism using localized in vivo C-13 NMR spectroscopy. The studies reviewed herein showed that anaplerosis is significant in brain, as is oxidative ATP generation in glia and the rate of glial glutamine synthesis attributed to the replenishment of the neuronal Glu pool and that brain glycogen metabolism is slow under resting conditions. This new modality promises to provide a new investigative tool to study aspects of normal and diseased brain hitherto unaccessible, such as the interplay between glutamatergic action, glucose and glycogen metabolism during brain activation, and the derangements thereof in patients with hepatic encephalopathy, neurodegenerative diseases and diabetes. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:143 / 154
页数:12
相关论文
共 84 条
[51]   INTERACTIONS BETWEEN NEURONS AND GLIA IN GLUTAMATE GLUTAMINE COMPARTMENTATION [J].
NICKLAS, WJ ;
ZEEVALK, G ;
HYNDMAN, A .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1987, 15 (02) :208-210
[52]   On the characteristics of functional magnetic resonance imaging of the brain [J].
Ogawa, S ;
Menon, RS ;
Kim, SG ;
Ugurbil, K .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1998, 27 :447-+
[53]   C-13 editing of glutamate in human brain using J-refocused coherence transfer spectroscopy at 4.1 T [J].
Pan, JLW ;
Mason, GF ;
Vaughan, JT ;
Chu, WJ ;
Zhang, YT ;
Hetherington, HP .
MAGNETIC RESONANCE IN MEDICINE, 1997, 37 (03) :355-358
[54]  
Pan JW, 2000, MAGNET RESON MED, V44, P673, DOI 10.1002/1522-2594(200011)44:5<673::AID-MRM3>3.0.CO
[55]  
2-L
[56]   GLUCOSE-TRANSPORT AND PHOSPHORYLATION - WHICH IS RATE-LIMITING FOR BRAIN GLUCOSE-UTILIZATION [J].
PARDRIDGE, WM .
ANNALS OF NEUROLOGY, 1994, 35 (05) :511-512
[57]  
Pfeuffer J, 1999, MAGNET RESON MED, V41, P1077, DOI 10.1002/(SICI)1522-2594(199906)41:6<1077::AID-MRM1>3.0.CO
[58]  
2-#
[59]   Extracellular-intracellular distribution of glucose and lactate in the rat brain assessed noninvasively by diffusion-weighted 1H nuclear magnetic resonance spectroscopy in vivo [J].
Pfeuffer, J ;
Tkác, I ;
Gruetter, R .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (04) :736-746
[60]   LACTATE RISE DETECTED BY H-1-NMR IN HUMAN VISUAL-CORTEX DURING PHYSIOLOGICAL STIMULATION [J].
PRICHARD, J ;
ROTHMAN, D ;
NOVOTNY, E ;
PETROFF, O ;
KUWABARA, T ;
AVISON, M ;
HOWSEMAN, A ;
HANSTOCK, C ;
SHULMAN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (13) :5829-5831