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DESCRIPTION (provided by applicant): We propose to develop a system for depth-resolved optical imaging of both voltage sensitive dyes (VSDs) and cortical hemodynamics, to enable study of three-dimensional (3D) neurovascular coupling in-vivo (rats). The relationship between neuronal activation and the corresponding hemodynamic response is of fundamental importance for understanding the mechanisms of functional activation, and particularly relevant to interpretation of functional magnetic resonance imaging (fMRI). Once introduced into the cortex, VSDs change their fluorescence proportionally to membrane potential, thereby indicating changes in neuronal activity. We have already developed a system for 3D optical imaging of oxy and deoxy-hemoglobin changes in rat cortex through thinned skull, called Laminar Optical Tomography (LOT). We are proposing to advance LOT.s hardware and algorithms to allow concurrent 3D imaging of rapid, small VSD fluorescence changes in addition to slower hemodynamic absorption changes. The LOT system is similar to a confocal microscope, but rather than varying focal depth, it detects multiply scattered light, which can be used to reconstruct images of structures to depths of >2mm with 100-200 micron resolution. VSD imaging to date has utilized 2D camera images of the cortex, which are very superficially weighted and provide no depth-resolution. Our motivation to simultaneously image VSDs and hemodynamics in 3D is twofold: 1) We hypothesize that to properly quantify the relationship between neural activity and hemodynamics, the two measures must be spatially co-localized in 3D: The depth-sensitivities of 2D fluorescence and absorption images are very different, and so their 2D pixels do not represent the same 3D locations in the cortex. 2) Electrophysiology has demonstrated that neuronal activity is layer-specific. A non-invasive way to study the 3D dynamics of neuronal activation as it moves and spreads between cortical layers would provide a completely new way to study cortical functional activity in-vivo. We propose to develop Fluorescent-LOT (PLOT) and then perform preliminary system testing using rats undergoing somatosensory stimulus. Improved understanding of the correlation between neuronal activity and fMRI signals is of prime importance to human brain imaging. The effects of abnormal pathologies on neurovascular coupling could provide new insights for treatment and prevention. The new system could also find applications in ocular, dermal, endoscopic and tumor imaging.
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DOI: 10.1016/j.neuroimage.2013.10.044
发表时间: 2014-02-15
期刊: NeuroImage
影响因子: 5.7
作者: [Rayshubskiy A, Wojtasiewicz TJ, Mikell CB, Bouchard MB, Timerman D, Youngerman BE, McGovern RA, Otten ML, Canoll P, McKhann GM 2nd, Hillman EM]
通讯作者: Hillman EM
DOI: 10.1364/boe.1.000780
发表时间: 2010-09-02
期刊: Biomedical optics express
影响因子: 3.4
作者: [Burgess SA, Ratner D, Chen BR, Hillman EM]
通讯作者: Hillman EM
DOI: 10.1364/ol.33.002164
发表时间: 2008-09-15
期刊: OPTICS LETTERS
影响因子: 3.6
作者: [Radosevich, Andrew J., Bouchard, Matthew B., Burgess, Sean A., Chen, Brenda R., Hillman, Elizabeth M. C.]
通讯作者: Hillman, Elizabeth M. C.
DOI: 10.1523/jneurosci.0058-09.2009
发表时间: 2009-03-18
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Karagiannis A, Gallopin T, Dávid C, Battaglia D, Geoffroy H, Rossier J, Hillman EM, Staiger JF, Cauli B]
通讯作者: Cauli B
11
    Cell type atlasing of whole human brains using HOLiS: an optimized pipeline for staining, clearing, imaging, and analysis
    • 批准号:
      10377810
    • 项目类别:
    • 资助金额:
      $912.19万
    • 财政年份:
      2021
    • 负责人:
      Elizabeth M. C. Hillman
    • 依托单位:
    Characterizing long-range cortical and subcortical dynamics in relation to corticospinal output and motor control
    • 批准号:
      10224732
    • 项目类别:
    • 资助金额:
      $48.37万
    • 财政年份:
      2017
    • 负责人:
      Elizabeth M. C. Hillman
    • 依托单位:
    Characterizing long-range cortical and subcortical dynamics in relation to corticospinal output and motor control
    SCAPE microscopy for high-speed in-vivo volumetric microscopy in behaving organisms
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