CEREBRAL METABOLIC COMPARTMENTATION AS REVEALED BY NUCLEAR-MAGNETIC-RESONANCE ANALYSIS OF D-[1-13C]GLUCOSE METABOLISM

被引:129
作者
SHANK, RP [1 ]
LEO, GC [1 ]
ZIELKE, HR [1 ]
机构
[1] UNIV MARYLAND,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21201
关键词
NUCLEAR MAGNETIC RESONANCE; 1-13C]GLUCOSE; GAMMA-AMINOBUTYRATE; GLUTAMATE; GLUTAMINE; ASTROCYTES;
D O I
10.1111/j.1471-4159.1993.tb03570.x
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
Nuclear magnetic resonance (NMR) was used to study the metabolic pathways involved in the conversion of glucose to glutamate, gamma-aminobutyrate (GABA), glutamine, and aspartate. D-[1-C-13]Glucose was administered to rats intraperitoneally, and 6, 1 5, 30, or 45 min later the rats were killed and extracts from the forebrain were prepared for C-13-NMR analysis and amino acid analysis. The absolute amount of C-13 present within each carbon-atom pool was determined for C-2, C-3, and C-4 of glutamate, glutamine, and GABA, for C-2 and C-3 of aspartate, and for C-3 of lactate. The natural abundance C-13 present in extracts from control rats was also determined for each of these compounds and for N-acetylaspartate and taurine. The pattern of labeling within glutamate and GABA indicates that these amino acids were synthesized primarily within compartments in which glucose was metabolized to pyruvate, followed by decarboxylation to acetyl-CoA for entry into the tricarboxylic acid cycle. In contrast, the labeling pattern for glutamine and aspartate indicates that appreciable amounts of these amino acids were synthesized within a compartment in which glucose was metabolized to pyruvate, followed by carboxylation to oxaloacetate. These results are consistent with the concept that pyruvate carboxylase and glutamine synthetase are glia-specific enzymes, and that this partially accounts for the unusual metabolic compartmentation in CNS tissues. The results of our study also support the concept that there are several pools of glutamate, with different metabolic turnover rates. Our results also are consistent with the concept that glutamine and/or a tricarboxylic acid cycle intermediate is supplied by astrocytes to neurons for replenishing the neurotransmitter pool of GABA. However, a similar role for astrocytes in replenishing the transmitter pool of glutamate was not substantiated, possibly due to difficulties in quantitating satellite peaks arising from C-13-C-13 coupling.
引用
收藏
页码:315 / 323
页数:9
相关论文
共 42 条
[1]   NEURONAL GLIAL METABOLISM UNDER DEPOLARIZING CONDITIONS A C-13-NMR STUDY [J].
BADARGOFFER, RS ;
BENYOSEPH, O ;
BACHELARD, HS ;
MORRIS, PG .
BIOCHEMICAL JOURNAL, 1992, 282 :225-230
[2]   CEREBRAL METABOLISM OF ACETATE AND GLUCOSE STUDIED BY C-13-NMR SPECTROSCOPY - A TECHNIQUE FOR INVESTIGATING METABOLIC COMPARTMENTATION IN THE BRAIN [J].
BADARGOFFER, RS ;
BACHELARD, HS ;
MORRIS, PG .
BIOCHEMICAL JOURNAL, 1990, 266 (01) :133-139
[3]   DETECTION OF METABOLITES IN RABBIT BRAIN BY C-13 NMR-SPECTROSCOPY FOLLOWING ADMINISTRATION OF [1-C-13]GLUCOSE [J].
BEHAR, KL ;
PETROFF, OAC ;
PRICHARD, JW ;
ALGER, JR ;
SHULMAN, RG .
MAGNETIC RESONANCE IN MEDICINE, 1986, 3 (06) :911-920
[4]  
BERL S, 1969, HDB NEUROCHEMISTRY, V1, P447
[5]   GLUTAMINE - MAJOR SUBSTRATE FOR NERVE-ENDINGS [J].
BRADFORD, HF ;
WARD, HK ;
THOMAS, AJ .
JOURNAL OF NEUROCHEMISTRY, 1978, 30 (06) :1453-1459
[6]   C-13 NUCLEAR MAGNETIC-RESONANCE EVIDENCE FOR GAMMA-AMINOBUTYRIC ACID FORMATION VIA PYRUVATE-CARBOXYLASE IN RAT-BRAIN - A METABOLIC BASIS FOR COMPARTMENTATION [J].
BRAINARD, JR ;
KYNER, E ;
ROSENBERG, GA .
JOURNAL OF NEUROCHEMISTRY, 1989, 53 (04) :1285-1292
[7]  
CERDAN S, 1990, J BIOL CHEM, V265, P12916
[8]  
CHANCE EM, 1983, J BIOL CHEM, V258, P3785
[9]   RELATIVE CONTRIBUTION OF CARBON DIOXIDE FIXATION AND ACETYL-COA PATHWAYS IN 2 NERVOUS TISSUES [J].
CHENG, SC ;
NAKAMURA, R ;
WAELSCH, H .
NATURE, 1967, 216 (5118) :928-&
[10]   THE FLUX FROM GLUCOSE TO GLUTAMATE IN THE RAT-BRAIN INVIVO AS DETERMINED BY H-1-OBSERVED, C-13-EDITED NMR-SPECTROSCOPY [J].
FITZPATRICK, SM ;
HETHERINGTON, HP ;
BEHAR, KL ;
SHULMAN, RG .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1990, 10 (02) :170-179