| Literature DB >> 28678440 |
Christopher S Medina1, Brett Manifold-Wheeler1, Aaron Gonzales1, Elaine L Bearer1,2.
Abstract
Magnetic resonance (MR) imaging provides a method to obtain anatomical information from the brain in vivo that is not typically available by optical imaging because of this organ's opacity. MR is nondestructive and obtains deep tissue contrast with 100-µm3 voxel resolution or better. Manganese-enhanced MRI (MEMRI) may be used to observe axonal transport and localized neural activity in the living rodent and avian brain. Such enhancement enables researchers to investigate differences in functional circuitry or neuronal activity in images of brains of different animals. Moreover, once MR images of a number of animals are aligned into a single matrix, statistical analysis can be done comparing MR intensities between different multi-animal cohorts comprising individuals from different mouse strains or different transgenic animals, or at different time points after an experimental manipulation. Although preprocessing steps for such comparisons (including skull stripping and alignment) are automated for human imaging, no such automated processing has previously been readily available for mouse or other widely used experimental animals, and most investigators use in-house custom processing. This protocol describes a stepwise method to perform such preprocessing for mouse. © 2017 by John Wiley & Sons, Inc.Entities:
Keywords: computational analysis and preprocessing; magnetic resonance imaging (MRI); manganese-enhanced magnetic resonance imaging (MEMRI); mouse and rodent brain; phenotyping brain anatomy
Mesh:
Year: 2017 PMID: 28678440 PMCID: PMC6195809 DOI: 10.1002/cpmb.40
Source DB: PubMed Journal: Curr Protoc Mol Biol ISSN: 1934-3647