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In Vivo Quantification of T₂ Anisotropy in White Matter Fibers in Marmoset Monkeys

Overview
Journal Neuroimage
Specialty Radiology
Date 2011 Sep 13
PMID 21906687
Citations 39
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Abstract

T₂-weighted MRI at high field is a promising approach for studying noninvasively the tissue structure and composition of the brain. However, the biophysical origin of T₂ contrast, especially in white matter, remains poorly understood. Recent work has shown that R₂ (=1/T₂) may depend on the tissue's orientation relative to the static magnetic field (B(0)) and suggested that this dependence could be attributed to local anisotropy in the magnetic properties of brain tissue. In the present work, we analyzed high-resolution, multi-gradient-echo images of in vivo marmoset brains at 7T, and compared them with ex vivo diffusion tensor images, to show that R₂ relaxation in white matter is highly sensitive to the fiber orientation relative to the main field. We directly demonstrate this orientation dependence by performing in vivo multi-gradient-echo experiments in two orthogonal brain positions, uncovering a nearly 50% change in the R₂ relaxation rate constant of the optic radiations. We attribute this substantial R₂ anisotropy to local subvoxel susceptibility effects arising from the highly ordered and anisotropic structure of the myelin sheath.

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References
1.
Bock N, Kocharyan A, Liu J, Silva A . Visualizing the entire cortical myelination pattern in marmosets with magnetic resonance imaging. J Neurosci Methods. 2009; 185(1):15-22. PMC: 2783340. DOI: 10.1016/j.jneumeth.2009.08.022. View

2.
Hikishima K, Quallo M, Komaki Y, Yamada M, Kawai K, Momoshima S . Population-averaged standard template brain atlas for the common marmoset (Callithrix jacchus). Neuroimage. 2010; 54(4):2741-9. DOI: 10.1016/j.neuroimage.2010.10.061. View

3.
Cremillieux Y, Ding S, Dunn J . High-resolution in vivo measurements of transverse relaxation times in rats at 7 Tesla. Magn Reson Med. 1998; 39(2):285-90. DOI: 10.1002/mrm.1910390216. View

4.
Reichenbach J, Venkatesan R, Schillinger D, Kido D, Haacke E . Small vessels in the human brain: MR venography with deoxyhemoglobin as an intrinsic contrast agent. Radiology. 1997; 204(1):272-7. DOI: 10.1148/radiology.204.1.9205259. View

5.
Yablonskiy D . Quantitation of intrinsic magnetic susceptibility-related effects in a tissue matrix. Phantom study. Magn Reson Med. 1998; 39(3):417-28. DOI: 10.1002/mrm.1910390312. View