Abstract
Purpose
MRI using manganese as a trans-synaptic axonal tracing agent can unveil dynamics of axonal transport in living subjects. We use this technology to test the hypotheses if impaired axonal transport is a significant pathophysiological process in aging and early Alzheimer’s disease (AD) and in part accounting for “selective vulnerability” of projection neurons in AD.
Methods
To allow quantitative assessment of axonal transport in vivo, we developed voxel-based statistical mapping technology as well as a tracer kinetic modeling method based on mass transport for manganese-enhanced MRI to estimate axonal transport rates in aging rats and AD transgenic mice.
Results
These techniques demonstrated manganese-enhanced signal changes in axonal projections of the olfactory tract and decreased axonal transport rates in rodent models of aging and AD.
Conclusion
Altered axonal transport may be a critical pathophysiological process in aging and AD. Manganese-enhanced MRI provides exciting opportunities for the investigations of altered axonal transport in AD and related disorders.
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The authors declare that they have no relevant financial or any other interests in this manuscript.
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Minoshima, S., Cross, D. In vivo imaging of axonal transport using MRI: aging and Alzheimer’s disease. Eur J Nucl Med Mol Imaging 35 (Suppl 1), 89–92 (2008). https://doi.org/10.1007/s00259-007-0707-8
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DOI: https://doi.org/10.1007/s00259-007-0707-8