Purpose: We present a novel approach that allows the estimation of morphological features of axonal fibers from data acquired in humans. This approach allows the assessment of white matter microscopic properties non-invasively with improved specificity.
Theory: The proposed approach is based on a biophysical model of Magnetic Resonance Imaging (MRI) data and of axonal conduction velocity estimates obtained with Electroencephalography (EEG). In a white matter tract of interest, these data depend on (1) the distribution of axonal radius [()] and (2) the g-ratio of the individual axons that compose this tract [()]. () is assumed to follow a Gamma distribution with mode and scale parameters, and θ, and () is described by a power law with parameters α and β.
Methods: MRI and EEG data were recorded from 14 healthy volunteers. MRI data were collected with a 3T scanner. MRI-measured g-ratio maps were computed and sampled along the visual transcallosal tract. EEG data were recorded using a 128-lead system with a visual Poffenberg paradigm. The interhemispheric transfer time and axonal conduction velocity were computed from the EEG current density at the group level. Using the MRI and EEG measures and the proposed model, we estimated morphological properties of axons in the visual transcallosal tract.
Results: The estimated interhemispheric transfer time was 11.72 ± 2.87 ms, leading to an average conduction velocity across subjects of 13.22 ± 1.18 m/s. Out of the 4 free parameters of the proposed model, we estimated θ - the width of the right tail of the axonal radius distribution - and β - the scaling factor of the axonal g-ratio, a measure of fiber myelination. Across subjects, the parameter θ was 0.40 ± 0.07 μm and the parameter β was 0.67 ± 0.02 μm.
Conclusion: The estimates of axonal radius and myelination are consistent with histological findings, illustrating the feasibility of this approach. The proposed method allows the measurement of the distribution of axonal radius and myelination within a white matter tract, opening new avenues for the combined study of brain structure and function, and for histological studies of the human brain.
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http://dx.doi.org/10.3389/fnins.2022.874023 | DOI Listing |
PLoS One
September 2024
Sano Centre for Computational Personalised Medicine, Kraków, Poland.
One of the key challenges in neuroscience is to generate the human nanoscale connectome which requires comprehensive knowledge of synaptome forming the neural microcircuits. The synaptic architecture determines limits of individual mental capacity and provides the framework for understanding neurologic disorders. Here, I address morphology modeling and storage estimation for the human synaptome at the nanoscale.
View Article and Find Full Text PDFbioRxiv
September 2024
Department of Ophthalmology, University of Pittsburgh, Pittsburgh PA, USA.
Insufficient oxygenation in the lamina cribrosa (LC) may contribute to axonal damage and glaucomatous vision loss. To understand the range of susceptibilities to glaucoma, we aimed to identify key factors influencing LC oxygenation and examine if these factors vary with anatomical differences between eyes. We reconstructed 3D, eye-specific LC vessel networks from histological sections of four healthy monkey eyes.
View Article and Find Full Text PDFJ R Soc Interface
July 2024
Department of Mathematics, Imperial College London, South Kensington, London SW7 2BZ, UK.
Biological systems such as axonal growth cones perform chemotaxis at micrometre-level length scales, where chemotactic molecules are sparse. Such systems lie outside the range of validity of existing models, which assume smoothly varying chemical gradients. We investigate the effect of introducing chemoattractant molecules by constructing a minimal dynamical model consisting of a chemotactic cell without internal memory.
View Article and Find Full Text PDFMagn Reson Med
November 2024
MR Physics, German Center for Neurodegenerative Diseases (DZNE) e.V, Bonn, Germany.
Purpose: To compare MR axon radius estimation in human white matter using a multiband spiral sequence combined with field monitoring to the current state-of-the-art echo-planar imaging (EPI)-based approach.
Methods: A custom multiband spiral sequence was used for diffusion-weighted imaging at ultra-high -values. Field monitoring and higher order image reconstruction were employed to greatly reduce artifacts in spiral images.
Magn Reson Med
June 2024
Danish Research Centre for Magnetic Resonance (DRCMR), Centre for Functional and Diagnostic Imaging and Research, Copenhagen University Hospital Amager and Hvidovre, Copenhagen, Denmark.
Purpose: This study aims to evaluate two distinct approaches for fiber radius estimation using diffusion-relaxation MRI data acquired in biomimetic microfiber phantoms that mimic hollow axons. The methods considered are the spherical mean power-law approach and a T-based pore size estimation technique.
Theory And Methods: A general diffusion-relaxation theoretical model for the spherical mean signal from water molecules within a distribution of cylinders with varying radii was introduced, encompassing the evaluated models as particular cases.
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