Literature DB >> 9751778

Interpreting functional imaging studies in terms of neurotransmitter cycling.

R G Shulman1, D L Rothman.   

Abstract

Functional imaging experiments, in particular positron-emission tomography and functional magnetic resonance imaging, can be analyzed either in psychological terms or on the basis of neuroscience. In the usual psychological interpretation, stimulations are designed to activate specific mental processes identified by cognitive psychology, which are then localized by the signals in functional imaging experiments. An alternate approach would be to analyze experiments in terms of the neurobiological processes responsible for the signals. Recent in vivo 13C NMR measurements of the glutamate-to-glutamine neurotransmitter cycling in rat and human brains facilitate a neuroscientific interpretation of functional imaging data in terms of neurobiological processes since incremental neurotransmitter flux showed a 1:1 stoichiometry with the incremental rate of glucose oxidation. Because functional imaging signals depend on brain energy consumption, a quantitative relationship can be established between the signal (S) and the specific neurochemical cerebral neurotransmitter activity (N) of glutamate-to-glutamine neurotransmitter cycling. The quantitation of neuronal activity proposed has implications for the psychological design and interpretation of functional imaging experiments. Measurements of the neurotransmitter cycling flux at rest in functional imaging experiments suggest that performing cognitive tasks and sensory stimulations increases neurotransmitter cycling by only 10-20%. Therefore it cannot be assumed that reference state activities are negligible, nor that they are constant during stimulation.

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Year:  1998        PMID: 9751778      PMCID: PMC21753          DOI: 10.1073/pnas.95.20.11993

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  34 in total

1.  Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.

Authors:  K K Kwong; J W Belliveau; D A Chesler; I E Goldberg; R M Weisskoff; B P Poncelet; D N Kennedy; B E Hoppel; M S Cohen; R Turner
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-15       Impact factor: 11.205

2.  Stoichiometric coupling of brain glucose metabolism and glutamatergic neuronal activity.

Authors:  N R Sibson; A Dhankhar; G F Mason; D L Rothman; K L Behar; R G Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  1998-01-06       Impact factor: 11.205

3.  Nonoxidative glucose consumption during focal physiologic neural activity.

Authors:  P T Fox; M E Raichle; M A Mintun; C Dence
Journal:  Science       Date:  1988-07-22       Impact factor: 47.728

4.  The [18F]fluorodeoxyglucose method for the measurement of local cerebral glucose utilization in man.

Authors:  M Reivich; D Kuhl; A Wolf; J Greenberg; M Phelps; T Ido; V Casella; J Fowler; E Hoffman; A Alavi; P Som; L Sokoloff
Journal:  Circ Res       Date:  1979-01       Impact factor: 17.367

Review 5.  Nuclear magnetic resonance imaging and spectroscopy of human brain function.

Authors:  R G Shulman; A M Blamire; D L Rothman; G McCarthy
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

6.  Brain function and blood flow.

Authors:  N A Lassen; D H Ingvar; E Skinhøj
Journal:  Sci Am       Date:  1978-10       Impact factor: 2.142

7.  Increased tricarboxylic acid cycle flux in rat brain during forepaw stimulation detected with 1H[13C]NMR.

Authors:  F Hyder; J R Chase; K L Behar; G F Mason; M Siddeek; D L Rothman; R G Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-23       Impact factor: 11.205

8.  In vivo 13C NMR measurements of cerebral glutamine synthesis as evidence for glutamate-glutamine cycling.

Authors:  N R Sibson; A Dhankhar; G F Mason; K L Behar; D L Rothman; R G Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-18       Impact factor: 11.205

9.  Localized 13C NMR spectroscopy in the human brain of amino acid labeling from D-[1-13C]glucose.

Authors:  R Gruetter; E J Novotny; S D Boulware; G F Mason; D L Rothman; G I Shulman; J W Prichard; R G Shulman
Journal:  J Neurochem       Date:  1994-10       Impact factor: 5.372

10.  Simultaneous determination of the rates of the TCA cycle, glucose utilization, alpha-ketoglutarate/glutamate exchange, and glutamine synthesis in human brain by NMR.

Authors:  G F Mason; R Gruetter; D L Rothman; K L Behar; R G Shulman; E J Novotny
Journal:  J Cereb Blood Flow Metab       Date:  1995-01       Impact factor: 6.200

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  38 in total

Review 1.  Functional magnetic resonance imaging: imaging techniques and contrast mechanisms.

Authors:  A M Howseman; R W Bowtell
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1999-07-29       Impact factor: 6.237

2.  Stimulated changes in localized cerebral energy consumption under anesthesia.

Authors:  R G Shulman; D L Rothman; F Hyder
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

3.  Cerebral energetics and the glycogen shunt: neurochemical basis of functional imaging.

Authors:  R G Shulman; F Hyder; D L Rothman
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-08       Impact factor: 11.205

4.  Cerebral energetics and spiking frequency: the neurophysiological basis of fMRI.

Authors:  Arien J Smith; Hal Blumenfeld; Kevin L Behar; Douglas L Rothman; Robert G Shulman; Fahmeed Hyder
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-19       Impact factor: 11.205

5.  Total neuroenergetics support localized brain activity: implications for the interpretation of fMRI.

Authors:  Fahmeed Hyder; Douglas L Rothman; Robert G Shulman
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-19       Impact factor: 11.205

6.  How does connectivity between cortical areas depend on brain size? Implications for efficient computation.

Authors:  Jan Karbowski
Journal:  J Comput Neurosci       Date:  2003 Nov-Dec       Impact factor: 1.621

Review 7.  Role of ongoing, intrinsic activity of neuronal populations for quantitative neuroimaging of functional magnetic resonance imaging-based networks.

Authors:  Fahmeed Hyder; Peter Herman; Basavaraju G Sanganahalli; Daniel Coman; Hal Blumenfeld; Douglas L Rothman
Journal:  Brain Connect       Date:  2011

8.  Neuronal correlate of BOLD signal fluctuations at rest: err on the side of the baseline.

Authors:  Fahmeed Hyder; Douglas L Rothman
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-08       Impact factor: 11.205

9.  Quantifying fluctuations of resting state networks using arterial spin labeling perfusion MRI.

Authors:  Weiying Dai; Gopal Varma; Rachel Scheidegger; David C Alsop
Journal:  J Cereb Blood Flow Metab       Date:  2015-11-05       Impact factor: 6.200

10.  Altered prefronto-striato-parietal network response to mental rotation in HIV.

Authors:  Brian C Schweinsburg; J Cobb Scott; Alecia Dager Schweinsburg; Joanna Jacobus; Rebecca J Theilmann; Larry R Frank; Erica Weber; Igor Grant; Steven Paul Woods
Journal:  J Neurovirol       Date:  2012-01-21       Impact factor: 2.643

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