Probing metabolite diffusion at ultra-short time scales in the mouse brain using optimized oscillating gradients and "short"-echo-time diffusion-weighted MRS

被引:23
|
作者
Ligneul, Clemence [1 ,2 ]
Valette, Julien [1 ,2 ]
机构
[1] MIRCen, Commissariat Energie Atom & Energies Alternat C, DRF, Inst Imagerie Biomed I2BM, F-92260 Fontenay Aux Roses, France
[2] Univ Paris Saclay, Univ Paris Sud, CNRS, Neurodegenerat Dis Lab,UMR 9199, F-92260 Fontenay Aux Roses, France
基金
欧洲研究理事会;
关键词
brain; diffusion; macromolecule; metabolite; motion artifact; MRS; oscillating gradient; MAGNETIC-RESONANCE-SPECTROSCOPY; INTRACELLULAR METABOLITES; SELF-DIFFUSION; FIBERS;
D O I
10.1002/nbm.3671
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Measuring diffusion at ultra-short time scales may yield information about short-range intracellular structure and cytosol viscosity. However, reaching such time scales usually requires oscillating gradients, which in turn imply long echo times TE. Here we propose a new kind of stretched oscillating gradient that allows us to increase diffusion-weighting b while preserving spectral and temporal properties of the gradient modulation. We used these optimized gradients to measure metabolite diffusion in the mouse brain down to effective diffusion times of 1 ms while keeping TE relatively short (60 ms). At such TE, a significant macromolecule signal could still be observed and used as an internal reference of approximately null diffusivity, which proved critical to discard datasets corrupted by some motion artifact. The methods introduced here may be useful to improve the accuracy and precision of metabolite apparent diffusion coefficient measurements with oscillating gradients.
引用
收藏
页数:10
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