Neurite orientation dispersion and density imaging of mouse brain microstructure

• Published in: Brain Structure and Function Vol. 224; no. 5; pp. 1797 - 1813
• Main Authors: Wang, Nian, Zhang, Jieying, Cofer, Gary, Qi, Yi, Anderson, Robert J., White, Leonard E., Allan Johnson, G.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.06.2019; Springer Nature B.V
• Subjects: Animal models; Animals; Axons; Biomedical and Life Sciences; Biomedicine; Brain - pathology; Brain - physiology; Brain Mapping - methods; Cell Biology; Corpus callosum; Cuprizone; Demyelination; Dendrites; Dendrites - pathology; Dendrites - physiology; Diffusion Magnetic Resonance Imaging - methods; Diffusion Tensor Imaging - methods; Image Processing, Computer-Assisted - methods; Magnetic resonance imaging; Male; Mice, Inbred C57BL; Myelin; Neurites - pathology; Neurites - physiology; Neuroimaging; Neurology; Neurosciences; Original Article; NODDI; Neurite density; Diffusion MRI; Cuprizone; Demyelination; Compressed sensing
• ISSN: 1863-2653; 1863-2661; 1863-2661; 0340-2061
• DOI: 10.1007/s00429-019-01877-x

Advanced biophysical models like neurite orientation dispersion and density imaging (NODDI) have been developed to estimate the microstructural complexity of voxels enriched in dendrites and axons for both in vivo and ex vivo studies. NODDI metrics derived from high spatial and angular resolution diffusion MRI using the fixed mouse brain as a reference template have not yet been reported due in part to the extremely long scan time required. In this study, we modified the three-dimensional diffusion-weighted spin-echo pulse sequence for multi-shell and undersampling acquisition to reduce the scan time. This allowed us to acquire several exhaustive datasets that would otherwise not be attainable. NODDI metrics were derived from a complex 8-shell diffusion (1000–8000 s/mm 2 ) dataset with 384 diffusion gradient-encoding directions at 50 µm isotropic resolution. These provided a foundation for exploration of tradeoffs among acquisition parameters. A three-shell acquisition strategy covering low, medium, and high b values with at least angular resolution of 64 is essential for ex vivo NODDI experiments. The good agreement between neurite density index (NDI) and the orientation dispersion index (ODI) with the subsequent histochemical analysis of myelin and neuronal density highlights that NODDI could provide new insight into the microstructure of the brain. Furthermore, we found that NDI is sensitive to microstructural variations in the corpus callosum using a well-established demyelination cuprizone model. The study lays the ground work for developing protocols for routine use of high-resolution NODDI method in characterizing brain microstructure in mouse models.