In vivo measurement of axon diameter distribution in the corpus callosum of rat brain

被引:318
作者
Barazany, Daniel [1 ]
Basser, Peter J. [2 ]
Assaf, Yaniv [1 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Neurobiol, IL-69978 Tel Aviv, Israel
[2] NICHHD, Sect Tissue Biophys & Biomimet, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院; 以色列科学基金会;
关键词
MRI; brain; corpus callosum; axon diameter distribution; diffusion; MYELINATED NERVE-FIBERS; DIFFUSION-TENSOR; WHITE-MATTER; RESTRICTED DIFFUSION; CONDUCTION-VELOCITY; MRI; DEMYELINATION; SPECTROSCOPY; MORPHOLOGY; HUMANS;
D O I
10.1093/brain/awp042
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Here, we present the first in vivo non-invasive measurement of the axon diameter distribution in the rat corpus callosum. Previously, this measurement was only possible using invasive histological methods. The axon diameter, along with other physical properties, such as the intra-axonal resistance, membrane resistance and capacitance etc. helps determine many important functional properties of nerves, such as their conduction velocity. In this work, we provide a novel magnetic resonance imaging method called AxCaliber, which can resolve the distinct signatures of trapped water molecules diffusing within axons as well as water molecules diffusing freely within the extra-axonal space. Using a series of diffusion weighted magnetic resonance imaging brain scans, we can reliably infer both the distribution of axon diameters and the volume fraction of these axons within each white matter voxel. We were able to verify the known microstructural variation along the corpus callosum of the rat from the anterior (genu) to posterior (splenium) regions. AxCaliber yields a narrow distribution centered 1 m in the genu and splenium and much broader distributions centered 3 m in the body of the corpus callosum. The axon diameter distribution found by AxCaliber is generally broader than those usually obtained by histology. One factor contributing to this difference is the significant tissue shrinkage that results from histological preparation. To that end, AxCaliber might provide a better estimate of the in vivo morphology of white matter. Being a magnetic resonance imaging based methodology, AxCaliber has the potential to be used in human scanners for morphological studies of white matter in normal and abnormal development, and white matter related diseases.
引用
收藏
页码:1210 / 1220
页数:11
相关论文
共 40 条
[31]  
Piven J, 1997, AM J PSYCHIAT, V154, P1051
[32]   SCHIZOPHRENIA, ABNORMAL CONNECTION, AND BRAIN EVOLUTION [J].
RANDALL, PL .
MEDICAL HYPOTHESES, 1983, 10 (03) :247-280
[33]  
Rice D, 2000, ENVIRON HEALTH PERSP, V108, P511, DOI 10.2307/3454543
[34]   ON THE RELATION BETWEEN FIBER DIAMETER AND CONDUCTION-VELOCITY IN MYELINATED NERVE-FIBERS [J].
RITCHIE, JM .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1982, 217 (1206) :29-35
[35]   Demyelination increases radial diffusivity in corpus callosum of mouse brain [J].
Song, SK ;
Yoshino, J ;
Le, TQ ;
Lin, SJ ;
Sun, SW ;
Cross, AH ;
Armstrong, RC .
NEUROIMAGE, 2005, 26 (01) :132-140
[36]   An analytical model of restricted diffusion in bovine optic nerve [J].
Stanisz, GJ ;
Szafer, A ;
Wright, GA ;
Henkelman, RM .
MAGNETIC RESONANCE IN MEDICINE, 1997, 37 (01) :103-111
[37]   Noninvasive detection of cuprizone induced axonal damage and demyelination in the mouse corpus callosum [J].
Sun, SW ;
Liang, HF ;
Trinkaus, K ;
Cross, AH ;
Armstrong, RC ;
Song, SK .
MAGNETIC RESONANCE IN MEDICINE, 2006, 55 (02) :302-308
[38]   Acquired lesions of the corpus callosum: MR imaging [J].
Uchino, A ;
Takase, Y ;
Nomiyama, K ;
Egashira, R ;
Kudo, S .
EUROPEAN RADIOLOGY, 2006, 16 (04) :905-914
[39]  
VIRTANEN J, 1984, ACTA OPHTHALMOL, V62, P577
[40]   DETERMINANTS OF CONDUCTION-VELOCITY IN MYELINATED NERVE-FIBERS [J].
WAXMAN, SG .
MUSCLE & NERVE, 1980, 3 (02) :141-150