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Journal Article

Water diffusion in rat brain in vivo as detected at very large b values is multicompartmental


Pfeuffer,  J
Department Physiology of Cognitive Processes, Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Pfeuffer, J., Provencher, S., & Gruetter, R. (1999). Water diffusion in rat brain in vivo as detected at very large b values is multicompartmental. MAGMA, 8, 98-108.

Cite as: http://hdl.handle.net/11858/00-001M-0000-0013-E74D-1
The diffusion-weighted signal attenuation of water in rat brain was measured with pulsed-field gradient NMR methods in a single voxel under in vivo and global ischemic conditions. The diffusion-attenuated water signal was observed in vivo at b-values of 300-ms/m2 (strength of diffusion weighting) and diffusion times up to 400-ms. A series of constant diffusion time (ct) experiments with varied gradient directions and diffusion times revealed a multiexponential decay with apparent diffusion coefficients (ADC) covering two orders of magnitude from 1 to 0.01-m2/ms. In a four-exponential fit the observed changes during global ischemia could be fully explained by changes in the relative volume fractions only with unchanged ADC's. An anisotropy of the ADC, detected at small b-values, was not observed for the ADC at large b-values, but for the concomitant volume fractions. An inverse Laplace Transform of the ct curves, performed with CONTIN, resulted in continuously distributed diffusion coefficients, for which the term 'diffusogram' is proposed. This approach was more appropriate than a discrete exponential model with four to six components, being related to the morphology of brain tissue and its cell size distribution. On the basis of an analytical, quantitative model it is suggested that the measured ADC at small b-values reflects mainly properties of the restricting boundaries, i.e. the relative volume fractions and the extracellular tortuosity, while the intrinsic intracellular diffusion constant and the exchange time are predicted to have minor influence.