Clemence Ligneul1,2, Marco Palombo1,2, and Julien Valette1,2
Diffusion-weighted magnetic
resonance spectroscopy is performed in a large voxel in the mouse brain at two
diffusion times, up to very high b-values. We combine different echo times and
mixing times to investigate the potential interplay between relaxation
properties and diffusion attenuation. Under current experimental conditions, we
don’t observe any significant dependence of metabolite diffusion properties on
TE/TM, except for water (and possibly NAA at very high b-values), which
supports the interpretation and modeling of metabolite diffusion based
primarily on geometry, irrespective of relaxation properties.