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SPECIFIC fMRI

From surrogate hemodynamics-based fMRI towards direct functional imaging of neural activity via sensing activity-induced cell swellings and neurotransmitter releases in vivo

Total Cost €

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EC-Contrib. €

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 SPECIFIC fMRI project word cloud

Explore the words cloud of the SPECIFIC fMRI project. It provides you a very rough idea of what is the project "SPECIFIC fMRI" about.

echo    predict    fidelity    relying    cellular    slow    neural    gt    sizes    neurotransmitter    complementary    harness    sense    nevertheless    noninvasively    global    active    transformed    pioneered    spin    couple    resolve    gradient    microstructural    detect    fmri    indirectly    relationships    noninvasive    experiments    mri    resonance    posit    uniform    hemodynamic    microstructure    tag    optogenetics    sensitive    probing    oscillating    underlying    ultrahigh    gaba    vivo    cell    detected    hemodynamics       sensitivity    spectral    recording    shift    relaxation    dynamics    conventional    technique    circuitry    regions    re    detects    indirect    robustly    function    signals    mrs    unprecedented    seconds    nature    activation    firings    functional    casual    neurovasculature    hence    true    couplings    magnetic    sufficiently    circuits    exquisite    simulations    stroboscopic    release    probe    independent    convey    detection    extraordinary    nogse    metabolic    elicited    signal    mapping    imaging    direct    metabolites    paradigm    mr    enhanced    subtle    glutamate       spectroscopy       snr    hypothesize    sensing    swellings    brain   

Project "SPECIFIC fMRI" data sheet

The following table provides information about the project.

Coordinator
FUNDACAO D. ANNA SOMMER CHAMPALIMAUD E DR. CARLOS MONTEZ CHAMPALIMAUD 

Organization address
address: AVENIDA BRASILIA, CENTRO DE INVESTIGACAO DA FUNDACAO CHAMPALIMAUD
city: LISBOA
postcode: 1400-038
website: http://fchampalimaud.org/

contact info
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 Coordinator Country Portugal [PT]
 Project website http://neuro.fchampalimaud.org/en/research/investigators/research-groups/group/Shemesh/
 Total cost 160˙635 €
 EC max contribution 160˙635 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-04-01   to  2017-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACAO D. ANNA SOMMER CHAMPALIMAUD E DR. CARLOS MONTEZ CHAMPALIMAUD PT (LISBOA) coordinator 160˙635.00

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 Project objective

Functional-Magnetic Resonance Imaging (fMRI) has transformed our understanding of brain function due to its ability to noninvasively tag ‘active’ brain regions. Nevertheless, fMRI only detects neural activity indirectly, by relying on slow hemodynamic couplings whose relationships with underlying neural activity are not fully known.

We have recently pioneered two unique MR approaches: Non-Uniform Oscillating-Gradient Spin-Echo (NOGSE) MRI and Relaxation Enhanced MR Spectroscopy (RE MRS). NOGSE-MRI is an exquisite microstructural probe, sensing cell sizes (l) with an unprecedented l^6 sensitivity (compared to l^2 in conventional approaches); RE MRS is a new spectral technique capable of recording metabolic signals with extraordinary fidelity at ultrahigh fields.

This proposal aims to harness these novel concepts for mapping neural activity directly, without relying on hemodynamics.

The specific objectives of this proposal are: (1) Mapping neural activity via sensing cell swellings upon activity: we hypothesize that NOGSE-fMRI can robustly sense subtle changes in cellular microstructure upon neural firings and hence convey neural activity directly. (2) Probing the nature of elicited activity via detection of neurotransmitter release: we posit that RE MRS is sufficiently sensitive to robustly detect changes in Glutamate and GABA signals upon activation. (3) Investigating widespread neural circuits in vivo via stroboscopic optogenetics: we propose to couple NOGSE-fMRI with optogenetics to resolve casual dynamics in global neural circuitry.

Simulations for NOGSE-fMRI predict >4% signal changes upon subtle cell swellings; further, our in vivo RE MRS experiments have detected metabolites with SNR>50 in only 6 seconds. Hence, these two complementary –and importantly, hemodynamics-independent– approaches will represent a true paradigm shift: from indirect detection of neurovasculature couplings towards direct and noninvasive mapping of neural activity in vivo.

 Publications

year authors and title journal last update
List of publications.
2017 Andrada IanuÅŸ, Noam Shemesh, Daniel C. Alexander, Ivana Drobnjak
Double oscillating diffusion encoding and sensitivity to microscopic anisotropy
published pages: 550-564, ISSN: 0740-3194, DOI: 10.1002/mrm.26393
Magnetic Resonance in Medicine 78/2 2019-06-13
2017 Daniel Nunes, Tomás L. Cruz, Sune N. Jespersen, Noam Shemesh
Mapping axonal density and average diameter using non-monotonic time-dependent gradient-echo MRI
published pages: 117-130, ISSN: 1090-7807, DOI: 10.1016/j.jmr.2017.02.017
Journal of Magnetic Resonance 277 2019-06-13
2017 Andrada IanuÅŸ, Noam Shemesh
Incomplete initial nutation diffusion imaging: An ultrafast, single-scan approach for diffusion mapping
published pages: , ISSN: 0740-3194, DOI: 10.1002/mrm.26894
Magnetic Resonance in Medicine 2019-06-13
2017 Sune Nørhøj Jespersen, Jonas Lynge Olesen, Brian Hansen, Noam Shemesh
Diffusion time dependence of microstructural parameters in fixed spinal cord
published pages: , ISSN: 1053-8119, DOI: 10.1016/j.neuroimage.2017.08.039
NeuroImage 2019-06-13

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