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State of the art direct 13C and indirect 1H-[13C] NMR spectroscopy in vivo. A practical guide
被引:86
作者:
de Graaf, Robin A.
[1
]
Rothman, Douglas L.
[1
]
Behar, Kevin L.
[2
]
机构:
[1] Yale Univ, Sch Med, Magnet Resonance Res Ctr, Dept Diagnost Radiol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Magnet Resonance Res Ctr, Dept Psychiat, New Haven, CT 06520 USA
关键词:
NMR spectroscopy;
direct C-13 detection;
indirect H-1-[C-13] detection;
broadband decoupling;
RF power deposition;
metabolism;
metabolic modeling;
BRAIN IN-VIVO;
NUCLEAR-MAGNETIC-RESONANCE;
KETOGLUTARATE GLUTAMATE EXCHANGE;
CEREBRAL GLUCOSE-UTILIZATION;
COMPOSITE PULSE SEQUENCES;
RAT-BRAIN;
POLARIZATION TRANSFER;
POPULATION-INVERSION;
GLYCOGEN-METABOLISM;
VOLUME COIL;
D O I:
10.1002/nbm.1761
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
Carbon-13 NMR spectroscopy in combination with C-13-labeled substrate infusion is a powerful technique for measuring a large number of metabolic fluxes noninvasively in vivo. It has been used to quantify glycogen synthesis rates, establish quantitative relationships between energy metabolism and neurotransmission, and evaluate the importance of different substrates. Measurements can, in principle, be performed through direct C-13 NMR detection or via indirect H-1-[C-13] NMR detection of the protons attached to C-13 nuclei. The choice of detection scheme and pulse sequence depends on the magnetic field strength, whereas substrate selection depends on metabolic pathways. C-13 NMR spectroscopy remains a challenging technique that requires several nonstandard hardware modifications, infusion of C-13-labeled substrates, and sophisticated processing and metabolic modeling. In this study, the various aspects of direct C-13 and indirect H-1-[C-13] NMR are reviewed with the aim of providing a practical guide. Copyright (C) 2011 John Wiley & Sons, Ltd.
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页码:958 / 972
页数:15
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