Skip Navigation



Cerebral Cortex Advance Access published online on July 24, 2008

Cerebral Cortex, doi:10.1093/cercor/bhn112
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
19/3/675    most recent
bhn112v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Baloch, S.
Right arrow Articles by Davatzikos, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Baloch, S.
Right arrow Articles by Davatzikos, C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org

Quantification of Brain Maturation and Growth Patterns in C57BL/6J Mice via Computational Neuroanatomy of Diffusion Tensor Images

Sajjad Baloch1, Ragini Verma1, Hao Huang2, Parmeshwar Khurd1, Sarah Clark3, Paul Yarowsky3,4, Ted Abel5, Susumu Mori2 and Christos Davatzikos1

1 Department of Radiology, University of Pennsylvania, PA 19104, USA, 2 Department of Radiology, Johns Hopkins University, Baltimore, MD 21287, USA, 3 School of Medicine, University of Maryland, Baltimore, MD 21250, USA, 4 Research Service, Department of Veterans Affairs Medical Center, Baltimore, MD 21201, USA, 5 Department of Biology, University of Pennsylvania, PA 19104-6021, USA

Address correspondence to Sajjad Baloch, PhD, Department of Radiology, University of Pennsylvania, PA 19104, USA. Email: sajjad.baloch{at}gmail.com.

Diffusion Tensor magnetic resonance imaging and computational neuroanatomy are used to quantify postnatal developmental patterns of C57BL/6J mouse brain. Changes in neuronal organization and myelination occurring as the brain matures into adulthood are examined, and a normative baseline is developed, against which transgenic mice may be compared in genotype–phenotype studies. In early postnatal days, gray matter–based cortical and hippocampal structures exhibit high water diffusion anisotropy, presumably reflecting the radial neuronal organization. Anisotropy drops rapidly within a week, indicating that the underlying brain tissue becomes more isotropic in orientation, possibly due to formation of a complex randomly intertwined web of dendrites. Gradual white matter anisotropy increase implies progressively more organized axonal pathways, likely reflecting the myelination of axons forming tightly packed fiber bundles. In contrast to the spatially complex pattern of tissue maturation, volumetric growth is somewhat uniform, with the cortex and the cerebellum exhibiting slightly more pronounced growth. Temporally, structural growth rates demonstrate an initial rapid volumetric increase in most structures, gradually tapering off to a steady state by about 20 days. Fiber maturation reaches steady state in about 10 days for the cortex, to 30–40 days for the corpus callosum, the hippocampus, and the internal and external capsules.

Key Words: computational neuroanatomy • development atlas • diffusion tensor imaging • fractional anisotropy • mouse brain


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.