| Literature DB >> 19041402 |
Damon Hyde1, Ruben de Kleine, Sarah A MacLaurin, Eric Miller, Dana H Brooks, Thomas Krucker, Vasilis Ntziachristos.
Abstract
The need to study molecular and functional parameters of Alzheimer's disease progression in animal models has led to the development of disease-specific fluorescent markers. However, curved optical interfaces and a highly heterogeneous internal structure make quantitative fluorescence imaging of the murine brain a particularly challenging tomographic problem. We investigated the integration of X-ray computed tomography (CT) information into a state-of-the-art fluorescence molecular tomography (FMT) scheme and establish that the dual-modality approach is essential for high fidelity reconstructions of distributed fluorescence within the murine brain, as compared to conventional fluorescence tomography. We employ this method in vivo using a fluorescent oxazine dye to quantify amyloid-beta plaque burden in transgenic APP23 mice modeling Alzheimer's disease. Multi-modal imaging allows for accurate signal localization and correlation of in vivo findings to ex vivo studies. The results point to FMT-CT as an essential tool for in vivo study of neurodegenerative disease in animal models and potentially humans.Entities:
Mesh:
Year: 2008 PMID: 19041402 DOI: 10.1016/j.neuroimage.2008.10.038
Source DB: PubMed Journal: Neuroimage ISSN: 1053-8119 Impact factor: 6.556