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  • 1
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Energy metabolism. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (335 pages)
    Edition: 1st ed.
    ISBN: 9780470020517
    DDC: 612.8/2
    Language: English
    Note: Intro -- Brain Energetics and Neuronal Activity -- Contents -- Contributors -- Foreword -- Section A: Background -- 1 Introduction -- 2 Energy Metabolism in Neural Tissues in vivo at Rest and in Functionally Altered States -- 3 Techniques-MRS, fMRI, (13)C NMR, Indirect Detection of (13)C -- 4 Metabolic Modeling Analysis of Brain Metabolism -- Section B: Neuroenergetics and Activity -- 5 Cerebral Energetics and Neurotransmitter Fluxes -- 6 NMR Studies of the Metabolism and Energetics of GABA Neurotransmitter Pathways -- 7 Neural Energy Consumption and the Representation of Mental Events -- 8 Imaging Cerebral Metabolic Rate of Oxygen Consumption (CMRO(2)) using (17)O NMR Approach at Ultrahigh Field -- 9 Deriving Changes in CMR(O2) from Calibrated fMRI -- 10 Relationship between CMR(O2) and Neuronal Activity -- Section C: Clinical Beginnings -- 11 NMR Studies of Bioenergetic Impairment in Human Epilepsy -- 12 MRS Studies of the Role of Altered Glutamate and GABA Neurotransmitter Metabolism in the Pathophysiology of Epilepsy -- 13 The Role of Altered Energetics of Neurotransmitter Systems in Psychiatric Disease -- Section D: Brain and Mind -- 14 Long-term Memory: Do Incremental Signals Reflect Engagement of Cognitive Processes? -- 15 Using fMRI to Study the Mind and Brain -- 16 Brain and Mind: an NMR Perspective -- 17 The Role of the NMR Baseline Signal in the Study of Consciousness: the Restless Brain -- Index.
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  • 2
    Online Resource
    Online Resource
    Cary :Oxford University Press, Incorporated,
    Keywords: Brain-Imaging. ; Neurosciences. ; Electronic books.
    Description / Table of Contents: The ability to image brain processes non-invasively has created a flood of experiments that fall into two categories--aiming to localize brain performance of abstractions like love, memory or intention--or to identify neuronal activities in response to observable behavior. This book discusses the experimental details and philosophical foundations distinguishing these two approaches, emphasizing the usefulness of the latter for planning and interpreting neuroimaging studies.
    Type of Medium: Online Resource
    Pages: 1 online resource (184 pages)
    Edition: 1st ed.
    ISBN: 9780199838738
    DDC: 612.82
    Language: English
    Note: Cover -- Contents -- Introduction -- 1. Mind and Matter -- 2. Biophysics: An Empirical Science -- 3. A Philosophical Background -- 4. Neuroscience: A Multidisciplinary, Multilevel Field -- 5. The State of Cognitive Neuroscience: An Over-Optimistic Theory -- 6. Brain Energy and the Work of Neurotransmission -- 7. Global Brain Energy Supports the State of Consciousness -- 8. Incremental Brain Energies and the Acts of Consciousness -- Epilogue. A Life in Humanities and Science -- Acknowledgments -- Index -- A -- B -- C -- D -- E -- F -- G -- H -- I -- J -- K -- L -- M -- N -- O -- P -- Q -- R -- S -- T -- U -- V -- W -- Y -- Z.
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  • 3
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Metabolism. ; Metabolism -- Research -- Methodology. ; Nuclear magnetic resonance spectroscopy. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (209 pages)
    Edition: 1st ed.
    ISBN: 9780470011492
    Language: English
    Note: Intro -- Metabolomics by In Vivo NMR -- Contents -- Contributors -- Foreword -- 1 Introduction -- 2 In Vivo NMR Spectroscopy - Techniques -- Direct Detection -- MRS -- Kinetics and Labels -- Fluxes -- Concentrations -- 3 Metabolic Control Analysis for the NMR Spectroscopist -- 4 MRS Studies of the Role of the Muscle Glycogen Synthesis Pathway in the Pathophysiology of Type 2 Diabetes -- 5 Phosphorylation of Allosteric Enzymes can serve Homeostasis rather than Control Flux: the Example of Glycogen Synthase -- 6 Regulation of Glycogen Metabolism in Muscle during Exercise -- 7 (13)C NMR Studies of Heart Glycogen Metabolism -- 8 Bioenergetics Implication of Metabolic Fluctuation during Muscle Contraction -- 9 Lactate, Glycogen and Fatigue -- 10 Futile Cycling in Yeast: How to Control Gluttony in the Midst of Plenty -- 11 Trehalose Energetics in Yeast Spores -- 12 Metabolic Networks in the Liver by (2)H and (13)C NMR -- 13 Summarized Reflections on Metabolism -- Index.
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  • 4
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: The effects of an acute intravenous infusion of ammonium acetate on rat cerebral glutamate and glutamine concentrations, energy metabolism, and intracellular pH were measured in vivo with 1H and 31P nuclear magnetic resonance (NMR). The level of blood ammonia maintained by the infusion protocol used in this study (∼ 500 μM, arterial blood) did not cause significant changes in arterial Pco2, Po2, or pH. Cerebral glutamate levels fell to at least 80% of the preinfusion value, whereas glutamine concentrations increased 170% relative to the preinfusion controls. The fall in brain glutamate concentrations followed a time course similar to that of the rise of brain glutamine. There were no detectable changes in the content of phosphocreatine (PCr) or nucleoside triphosphates (NTP), within the brain regions contributing to the sensitive volume of the surface coil, during the ammonia infusion. Intracellular pH, estimated from the chemical shift of the inorganic phosphate resonance relative to the resonance of PCr in the 31P spectrum, was also unchanged during the period of hyperammonemia. 1H spectra, specifically edited to allow quantitation of the brain lactate content, indicated that lactate rose steadily during the ammonia infusion. Detectable increases in brain lactate levels were observed ∼ 10 min after the start of the ammonia infusion and by 50 min of infusion had more than doubled. Spectra acquired from rats that received a control infusion of sodium acetate were not different from the spectra acquired prior to the infusion of either ammonium or sodium acetate. The results reported here support earlier findings that an increased blood ammonia concentration has a pronounced effect on the brain concentrations of two important amino acids, glutamate and glutamine. They also provide in vivo evidence for the absence of a sustained alteration in either brain intracellular pH or in the concentration of high-energy phosphate compounds during a period of acute hyperammonemia. The technique of in vivo NMR spectroscopy permits multiple, simultaneous measurements of important intermediary and energy metabolites in a single animal, in real time, prior to and during the systemic perturbation.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Cerebral metabolism of d[1-13C]glucose was studied with localized 13C NMR spectroscopy during intravenous infusion of enriched [1-13C]glucose in four healthy subjects. The use of three-dimensional localization resulted in the complete elimination of triacylglycerol resonance that originated in scalp and subcutaneous fat. The sensitivity and resolution were sufficient to allow 4 min of time-resolved observation of label incorporation into the C3 and C4 resonances of glutamate and C4 of glutamine, as well as C3 of aspartate with lower time resolution. [4-13C]Glutamate labeled rapidly reaching close to maximum labeling at 60 min. The label flow into [3-13C]glutamate clearly lagged behind that of [4-13C]glutamate and peaked at t = 110–140 min. Multiplets due to homonuclear 13C-13C coupling between the C3 and C4 peaks of the glutamate molecule were observed in vivo. Isotopomer analysis of spectra acquired between 120 and 180 min yielded a 13C isotopic fraction at C4 glutamate of 27 ± 2% (n = 4), which was slightly less than one-half the enrichment of the C1 position of plasma glucose (63 ± 1%), p 〈 0.05. By comparison with an external standard the total amount of [4-13C]glutamate was directly quantified to be 2.4 ± 0.1 µmol/ml-brain. Together with the isotopomer data this gave a calculated brain glutamate concentration of 9.1 ± 0.7 µmol/ml, which agrees with previous estimates of total brain glutamate concentrations. The agreement suggests that essentially all of the brain glutamate is derived from glucose in healthy human brain.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The aims of this study were twofold: (i) to determine quantitatively the contribution of glutamate/glutamine cycling to total astrocyte/neuron substrate trafficking for the replenishment of neurotransmitter glutamate; and (ii) to determine the relative contributions of anaplerotic flux and glutamate/glutamine cycling to total glutamine synthesis. In this work in vivo and in vitro13C NMR spectroscopy were used, with a [2-13C]glucose or [5-13C]glucose infusion, to determine the rates of glutamate/glutamine cycling, de novo glutamine synthesis via anaplerosis, and the neuronal and astrocytic tricarboxylic acid cycles in the rat cerebral cortex. The rate of glutamate/glutamine cycling measured in this study is compared with that determined from re-analysis of 13C NMR data acquired during a [1-13C]glucose infusion. The excellent agreement between these rates supports the hypothesis that glutamate/glutamine cycling is a major metabolic flux (∼0.20 µmol/min/g) in the cerebral cortex of anesthetized rats and the predominant pathway of astrocyte/neuron trafficking of neurotransmitter glutamate precursors. Under normoammonemic conditions anaplerosis was found to comprise 19–26% of the total glutamine synthesis, whilst this fraction increased significantly during hyperammonemia (∼32%). These findings indicate that anaplerotic glutamine synthesis is coupled to nitrogen removal from the brain (ammonia detoxification) under hyperammonemic conditions.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 29 (1990), S. 6815-6820 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 32 (1993), S. 9417-9422 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 22 (1983), S. 1087-1094 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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