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Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation.

Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation. Research Abstract Details 

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  • Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation. Abstract Text:

    elizabeth m c hillmanElizabeth M C Hillman,anna devorAnna Devor,matthew b bouchardMatthew B Bouchard,andrew k dunnAndrew K Dunn,g w kraussG W Krauss,jesse skochJesse Skoch,brian j bacskaiBrian J Bacskai,anders m daleAnders M Dale,david a boasDavid A Boas,

    The cortical hemodynamic response to somatosensory stimulus is investigated at the level of individual vascular compartments using both depth-resolved optical imaging and in-vivo two-photon microscopy. We utilize a new imaging and spatiotemporal analysis approach that exploits the different characteristic dynamics of responding arteries, arterioles, capillaries and veins to isolate their three-dimensional spatial extent within the cortex. This spatial delineation is validated using vascular casts. Temporal delineation is supported by in-vivo two-photon microscopy of the temporal dynamics and vascular mechanisms of the arteriolar and venous responses. Using these techniques we have been able to characterize the roles of the different vascular compartments in generating and controlling the hemodynamic response to somatosensory stimulus. We find that changes in arteriolar total hemoglobin concentration agree well with arteriolar dilation dynamics, which in turn correspond closely with changes in venous blood flow. For 4-s stimuli, we see only small changes in venous hemoglobin concentration, and do not detect measurable dilation or ballooning in the veins. Instead, we see significant evidence of capillary hyperemia. We compare our findings to historical observations of the composite hemodynamic response from other modalities including functional magnetic resonance imaging. Implications of our results are discussed with respect to mathematical models of cortical hemodynamics, and to current theories on the mechanisms underlying neurovascular coupling. We also conclude that our spatiotemporal analysis approach is capable of isolating and localizing signals from the capillary bed local to neuronal activation, and holds promise for improving the specificity of other hemodynamic imaging modalities.

    Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation. Publishing Authors By Initials

    em hillmanEM Hillman,a devorA Devor,mb bouchardMB Bouchard,ak dunnAK Dunn,gw kraussGW Krauss,j skochJ Skoch,bj bacskaiBJ Bacskai,am daleAM Dale,da boasDA Boas,

    For similar vasodilation research abstracts see: vasodilation research

    PUBMED ID PMID:

    MEDLINE DATE:

    Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: NeuroImage

    VOLUME: 35

    Page Numbers: 89-104

    Journal Abbreviation: Neuroimage

    ISSN: 1053-8119

    DAY: 11

    MONTH: 01

    YEAR: 2007

    Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9215515

    Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation. Keywords Mesh Terms:

    KEYWORDS: Vasodilation

    MESH TERMS: physiology

    Chemical & Substance for Abstract: Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation. Information

    Substance Name: Oxygen

    Registry Number: 7782-44-7

    Grant and Affiliation Information for Depth-resolved optical imaging and microscopy of vascular compartment dynamics during somatosensory stimulation.

    AFFILIATION: Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Building 149, 13th Street, Charlestown, MA 02129, USA. eh2245@columbia.edu <eh2245@columbia.edu>

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NINDS

    GRANT: R21NS053684

    ACRONYM: NS

    MEDLINETA: Neuroimage

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    ACCESSION NUMBER:

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